U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Protein

Items: 1 to 20 of 438

1.

rs1489586270 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    11:13354384 (GRCh38)
    11:13375931 (GRCh37)
    Canonical SPDI:
    NC_000011.10:13354383:A:G
    Gene:
    ARNTL (Varview), LOC124902636 (Varview)
    Functional Consequence:
    coding_sequence_variant,500B_downstream_variant,non_coding_transcript_variant,genic_upstream_transcript_variant,downstream_transcript_variant,missense_variant,5_prime_UTR_variant,upstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0./0 (ALFA)
    G=0.000004/1 (GnomAD_exomes)
    G=0.000008/2 (TOPMED)
    HGVS:
    NC_000011.10:g.13354384A>G, NC_000011.9:g.13375931A>G, NM_001178.6:c.76A>G, NM_001178.5:c.76A>G, NM_001178.4:c.76A>G, XM_011520105.4:c.205A>G, XM_011520105.3:c.205A>G, XM_011520105.2:c.205A>G, XM_011520105.1:c.76A>G, XM_011520107.4:c.205A>G, XM_011520107.3:c.205A>G, XM_011520107.2:c.205A>G, XM_011520107.1:c.76A>G, XM_017017738.3:c.205A>G, XM_017017738.2:c.205A>G, XM_017017738.1:c.205A>G, XM_017017739.3:c.205A>G, XM_017017739.2:c.205A>G, XM_017017739.1:c.205A>G, NM_001030273.3:c.-125A>G, NM_001030273.2:c.-125A>G, NM_001030273.1:c.-125A>G, NM_001030272.3:c.76A>G, NM_001030272.2:c.76A>G, NM_001030272.1:c.76A>G, NR_147789.2:n.417A>G, NR_147789.1:n.480A>G, NR_147787.2:n.417A>G, NR_147787.1:n.480A>G, NM_001351812.2:c.-100A>G, NM_001351812.1:c.-100A>G, NR_147790.2:n.417A>G, NR_147790.1:n.480A>G, NR_147791.2:n.417A>G, NR_147791.1:n.480A>G, NR_147788.2:n.472A>G, NR_147788.1:n.535A>G, NM_001351823.2:c.-125A>G, NM_001351823.1:c.-125A>G, NM_001351808.2:c.-125A>G, NM_001351808.1:c.-125A>G, NM_001351809.2:c.-100A>G, NM_001351809.1:c.-100A>G, NM_001351818.2:c.-125A>G, NM_001351818.1:c.-125A>G, NM_001351820.2:c.-118A>G, NM_001351820.1:c.-118A>G, NR_147785.2:n.417A>G, NR_147785.1:n.480A>G, NR_147786.2:n.417A>G, NR_147786.1:n.480A>G, NM_001351813.2:c.-125A>G, NM_001351813.1:c.-125A>G, NM_001351816.2:c.-125A>G, NM_001351816.1:c.-125A>G, NM_001351814.2:c.76A>G, NM_001351814.1:c.76A>G, NM_001297724.2:c.-118A>G, NM_001297724.1:c.-118A>G, NM_001297719.2:c.76A>G, NM_001297719.1:c.76A>G, NM_001351807.2:c.76A>G, NM_001351807.1:c.76A>G, NM_001351819.2:c.76A>G, NM_001351819.1:c.76A>G, NM_001351821.2:c.-125A>G, NM_001351821.1:c.-125A>G, NM_001297722.2:c.76A>G, NM_001297722.1:c.76A>G, NM_001351811.2:c.-667A>G, NM_001351811.1:c.-667A>G, NM_001351805.2:c.76A>G, NM_001351805.1:c.76A>G, NM_001351806.2:c.76A>G, NM_001351806.1:c.76A>G, NM_001351822.2:c.-125A>G, NM_001351822.1:c.-125A>G, XM_011520109.2:c.76A>G, XM_011520109.1:c.76A>G, XM_017017741.2:c.76A>G, XM_017017741.1:c.76A>G, NM_001351824.2:c.76A>G, NM_001351824.1:c.76A>G, NM_001351815.2:c.76A>G, NM_001351815.1:c.76A>G, NM_001351810.2:c.76A>G, NM_001351810.1:c.76A>G, NM_001351817.2:c.76A>G, NM_001351817.1:c.76A>G, XM_047426956.1:c.76A>G, NM_001351804.1:c.76A>G, XM_047426953.1:c.76A>G, XM_047426955.1:c.76A>G, XM_047426952.1:c.76A>G, XM_047426954.1:c.76A>G, XM_047426957.1:c.205A>G, XM_047426958.1:c.205A>G, NP_001169.3:p.Ser26Gly, XP_011518407.2:p.Ser69Gly, XP_011518409.2:p.Ser69Gly, XP_016873227.1:p.Ser69Gly, XP_016873228.1:p.Ser69Gly, NP_001025443.1:p.Ser26Gly, NP_001338743.1:p.Ser26Gly, NP_001284648.1:p.Ser26Gly, NP_001338736.1:p.Ser26Gly, NP_001338748.1:p.Ser26Gly, NP_001284651.1:p.Ser26Gly, NP_001338734.1:p.Ser26Gly, NP_001338735.1:p.Ser26Gly, XP_011518411.1:p.Ser26Gly, XP_016873230.1:p.Ser26Gly, NP_001338753.1:p.Ser26Gly, NP_001338744.1:p.Ser26Gly, NP_001338739.1:p.Ser26Gly, NP_001338746.1:p.Ser26Gly, XP_047282912.1:p.Ser26Gly, NP_001338733.1:p.Ser26Gly, XP_047282909.1:p.Ser26Gly, XP_047282911.1:p.Ser26Gly, XP_047282908.1:p.Ser26Gly, XP_047282910.1:p.Ser26Gly, XP_047282913.1:p.Ser69Gly, XP_047282914.1:p.Ser69Gly

    2.

    rs1487477840 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>G [Show Flanks]
      Chromosome:
      11:13372339 (GRCh38)
      11:13393886 (GRCh37)
      Canonical SPDI:
      NC_000011.10:13372338:A:G
      Gene:
      ARNTL (Varview)
      Functional Consequence:
      coding_sequence_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant,missense_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      G=0./0 (ALFA)
      G=0.000007/1 (GnomAD)
      G=0.000015/4 (TOPMED)
      HGVS:
      NC_000011.10:g.13372339A>G, NC_000011.9:g.13393886A>G, NM_001178.6:c.994A>G, NM_001178.5:c.994A>G, NM_001178.4:c.994A>G, XM_011520105.4:c.1123A>G, XM_011520105.3:c.1123A>G, XM_011520105.2:c.1123A>G, XM_011520105.1:c.994A>G, XM_011520107.4:c.1123A>G, XM_011520107.3:c.1123A>G, XM_011520107.2:c.1123A>G, XM_011520107.1:c.994A>G, XM_017017738.3:c.1126A>G, XM_017017738.2:c.1126A>G, XM_017017738.1:c.1126A>G, XM_017017739.3:c.1126A>G, XM_017017739.2:c.1126A>G, XM_017017739.1:c.1126A>G, NM_001030273.3:c.865A>G, NM_001030273.2:c.865A>G, NM_001030273.1:c.865A>G, NM_001030272.3:c.994A>G, NM_001030272.2:c.994A>G, NM_001030272.1:c.994A>G, NR_147789.2:n.1406A>G, NR_147789.1:n.1469A>G, NR_147787.2:n.1338A>G, NR_147787.1:n.1401A>G, NM_001351812.2:c.946A>G, NM_001351812.1:c.946A>G, NR_147790.2:n.1409A>G, NR_147790.1:n.1472A>G, NR_147791.2:n.1406A>G, NR_147791.1:n.1469A>G, NR_147788.2:n.1390A>G, NR_147788.1:n.1453A>G, NM_001351823.2:c.868A>G, NM_001351823.1:c.868A>G, NM_001351808.2:c.868A>G, NM_001351808.1:c.868A>G, NM_001351809.2:c.946A>G, NM_001351809.1:c.946A>G, NM_001351818.2:c.865A>G, NM_001351818.1:c.865A>G, NM_001351820.2:c.868A>G, NM_001351820.1:c.868A>G, NR_147785.2:n.1338A>G, NR_147785.1:n.1401A>G, NR_147786.2:n.1335A>G, NR_147786.1:n.1398A>G, NM_001351813.2:c.865A>G, NM_001351813.1:c.865A>G, NM_001351816.2:c.868A>G, NM_001351816.1:c.868A>G, NM_001351814.2:c.997A>G, NM_001351814.1:c.997A>G, NM_001297724.2:c.868A>G, NM_001297724.1:c.868A>G, NM_001297719.2:c.997A>G, NM_001297719.1:c.997A>G, NM_001351807.2:c.997A>G, NM_001351807.1:c.997A>G, NM_001351819.2:c.994A>G, NM_001351819.1:c.994A>G, NM_001351821.2:c.868A>G, NM_001351821.1:c.868A>G, NM_001297722.2:c.997A>G, NM_001297722.1:c.997A>G, NM_001351811.2:c.247A>G, NM_001351811.1:c.247A>G, NM_001351805.2:c.958A>G, NM_001351805.1:c.958A>G, NM_001351806.2:c.955A>G, NM_001351806.1:c.955A>G, NM_001351822.2:c.868A>G, NM_001351822.1:c.868A>G, XM_011520109.2:c.997A>G, XM_011520109.1:c.997A>G, XM_017017741.2:c.994A>G, XM_017017741.1:c.994A>G, NM_001351824.2:c.997A>G, NM_001351824.1:c.997A>G, NM_001351815.2:c.994A>G, NM_001351815.1:c.994A>G, XM_047426956.1:c.997A>G, NM_001351804.1:c.994A>G, XM_024448522.1:c.946A>G, XM_047426953.1:c.997A>G, XM_047426955.1:c.997A>G, XM_047426952.1:c.997A>G, XM_047426954.1:c.997A>G, XM_047426957.1:c.1126A>G, NP_001169.3:p.Ile332Val, XP_011518407.2:p.Ile375Val, XP_011518409.2:p.Ile375Val, XP_016873227.1:p.Ile376Val, XP_016873228.1:p.Ile376Val, NP_001025444.1:p.Ile289Val, NP_001025443.1:p.Ile332Val, NP_001338741.1:p.Ile316Val, NP_001338752.1:p.Ile290Val, NP_001338737.1:p.Ile290Val, NP_001338738.1:p.Ile316Val, NP_001338747.1:p.Ile289Val, NP_001338749.1:p.Ile290Val, NP_001338742.1:p.Ile289Val, NP_001338745.1:p.Ile290Val, NP_001338743.1:p.Ile333Val, NP_001284653.1:p.Ile290Val, NP_001284648.1:p.Ile333Val, NP_001338736.1:p.Ile333Val, NP_001338748.1:p.Ile332Val, NP_001338750.1:p.Ile290Val, NP_001284651.1:p.Ile333Val, NP_001338740.1:p.Ile83Val, NP_001338734.1:p.Ile320Val, NP_001338735.1:p.Ile319Val, NP_001338751.1:p.Ile290Val, XP_011518411.1:p.Ile333Val, XP_016873230.1:p.Ile332Val, NP_001338753.1:p.Ile333Val, NP_001338744.1:p.Ile332Val, XP_047282912.1:p.Ile333Val, NP_001338733.1:p.Ile332Val, XP_024304290.1:p.Ile316Val, XP_047282909.1:p.Ile333Val, XP_047282911.1:p.Ile333Val, XP_047282908.1:p.Ile333Val, XP_047282910.1:p.Ile333Val, XP_047282913.1:p.Ile376Val

      3.

      rs1486537170 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>A [Show Flanks]
        Chromosome:
        11:13372316 (GRCh38)
        11:13393863 (GRCh37)
        Canonical SPDI:
        NC_000011.10:13372315:T:A
        Gene:
        ARNTL (Varview)
        Functional Consequence:
        coding_sequence_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant,missense_variant
        Validated:
        by frequency
        MAF:
        A=0.000004/1 (GnomAD_exomes)
        HGVS:
        NC_000011.10:g.13372316T>A, NC_000011.9:g.13393863T>A, NM_001178.6:c.971T>A, NM_001178.5:c.971T>A, NM_001178.4:c.971T>A, XM_011520105.4:c.1100T>A, XM_011520105.3:c.1100T>A, XM_011520105.2:c.1100T>A, XM_011520105.1:c.971T>A, XM_011520107.4:c.1100T>A, XM_011520107.3:c.1100T>A, XM_011520107.2:c.1100T>A, XM_011520107.1:c.971T>A, XM_017017738.3:c.1103T>A, XM_017017738.2:c.1103T>A, XM_017017738.1:c.1103T>A, XM_017017739.3:c.1103T>A, XM_017017739.2:c.1103T>A, XM_017017739.1:c.1103T>A, NM_001030273.3:c.842T>A, NM_001030273.2:c.842T>A, NM_001030273.1:c.842T>A, NM_001030272.3:c.971T>A, NM_001030272.2:c.971T>A, NM_001030272.1:c.971T>A, NR_147789.2:n.1383T>A, NR_147789.1:n.1446T>A, NR_147787.2:n.1315T>A, NR_147787.1:n.1378T>A, NM_001351812.2:c.923T>A, NM_001351812.1:c.923T>A, NR_147790.2:n.1386T>A, NR_147790.1:n.1449T>A, NR_147791.2:n.1383T>A, NR_147791.1:n.1446T>A, NR_147788.2:n.1367T>A, NR_147788.1:n.1430T>A, NM_001351823.2:c.845T>A, NM_001351823.1:c.845T>A, NM_001351808.2:c.845T>A, NM_001351808.1:c.845T>A, NM_001351809.2:c.923T>A, NM_001351809.1:c.923T>A, NM_001351818.2:c.842T>A, NM_001351818.1:c.842T>A, NM_001351820.2:c.845T>A, NM_001351820.1:c.845T>A, NR_147785.2:n.1315T>A, NR_147785.1:n.1378T>A, NR_147786.2:n.1312T>A, NR_147786.1:n.1375T>A, NM_001351813.2:c.842T>A, NM_001351813.1:c.842T>A, NM_001351816.2:c.845T>A, NM_001351816.1:c.845T>A, NM_001351814.2:c.974T>A, NM_001351814.1:c.974T>A, NM_001297724.2:c.845T>A, NM_001297724.1:c.845T>A, NM_001297719.2:c.974T>A, NM_001297719.1:c.974T>A, NM_001351807.2:c.974T>A, NM_001351807.1:c.974T>A, NM_001351819.2:c.971T>A, NM_001351819.1:c.971T>A, NM_001351821.2:c.845T>A, NM_001351821.1:c.845T>A, NM_001297722.2:c.974T>A, NM_001297722.1:c.974T>A, NM_001351811.2:c.224T>A, NM_001351811.1:c.224T>A, NM_001351805.2:c.935T>A, NM_001351805.1:c.935T>A, NM_001351806.2:c.932T>A, NM_001351806.1:c.932T>A, NM_001351822.2:c.845T>A, NM_001351822.1:c.845T>A, XM_011520109.2:c.974T>A, XM_011520109.1:c.974T>A, XM_017017741.2:c.971T>A, XM_017017741.1:c.971T>A, NM_001351824.2:c.974T>A, NM_001351824.1:c.974T>A, NM_001351815.2:c.971T>A, NM_001351815.1:c.971T>A, XM_047426956.1:c.974T>A, NM_001351804.1:c.971T>A, XM_024448522.1:c.923T>A, XM_047426953.1:c.974T>A, XM_047426955.1:c.974T>A, XM_047426952.1:c.974T>A, XM_047426954.1:c.974T>A, XM_047426957.1:c.1103T>A, NP_001169.3:p.Val324Asp, XP_011518407.2:p.Val367Asp, XP_011518409.2:p.Val367Asp, XP_016873227.1:p.Val368Asp, XP_016873228.1:p.Val368Asp, NP_001025444.1:p.Val281Asp, NP_001025443.1:p.Val324Asp, NP_001338741.1:p.Val308Asp, NP_001338752.1:p.Val282Asp, NP_001338737.1:p.Val282Asp, NP_001338738.1:p.Val308Asp, NP_001338747.1:p.Val281Asp, NP_001338749.1:p.Val282Asp, NP_001338742.1:p.Val281Asp, NP_001338745.1:p.Val282Asp, NP_001338743.1:p.Val325Asp, NP_001284653.1:p.Val282Asp, NP_001284648.1:p.Val325Asp, NP_001338736.1:p.Val325Asp, NP_001338748.1:p.Val324Asp, NP_001338750.1:p.Val282Asp, NP_001284651.1:p.Val325Asp, NP_001338740.1:p.Val75Asp, NP_001338734.1:p.Val312Asp, NP_001338735.1:p.Val311Asp, NP_001338751.1:p.Val282Asp, XP_011518411.1:p.Val325Asp, XP_016873230.1:p.Val324Asp, NP_001338753.1:p.Val325Asp, NP_001338744.1:p.Val324Asp, XP_047282912.1:p.Val325Asp, NP_001338733.1:p.Val324Asp, XP_024304290.1:p.Val308Asp, XP_047282909.1:p.Val325Asp, XP_047282911.1:p.Val325Asp, XP_047282908.1:p.Val325Asp, XP_047282910.1:p.Val325Asp, XP_047282913.1:p.Val368Asp

        4.

        rs1483665028 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>G [Show Flanks]
          Chromosome:
          11:13358518 (GRCh38)
          11:13380065 (GRCh37)
          Canonical SPDI:
          NC_000011.10:13358517:C:G
          Gene:
          ARNTL (Varview), LOC124902636 (Varview)
          Functional Consequence:
          intron_variant,non_coding_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant,5_prime_UTR_variant,upstream_transcript_variant,missense_variant
          Validated:
          by frequency
          MAF:
          G=0.000004/1 (GnomAD_exomes)
          HGVS:
          NC_000011.10:g.13358518C>G, NC_000011.9:g.13380065C>G, NM_001178.6:c.306C>G, NM_001178.5:c.306C>G, NM_001178.4:c.306C>G, XM_011520105.4:c.435C>G, XM_011520105.3:c.435C>G, XM_011520105.2:c.435C>G, XM_011520105.1:c.306C>G, XM_011520107.4:c.435C>G, XM_011520107.3:c.435C>G, XM_011520107.2:c.435C>G, XM_011520107.1:c.306C>G, XM_017017738.3:c.435C>G, XM_017017738.2:c.435C>G, XM_017017738.1:c.435C>G, XM_017017739.3:c.435C>G, XM_017017739.2:c.435C>G, XM_017017739.1:c.435C>G, NM_001030273.3:c.177C>G, NM_001030273.2:c.177C>G, NM_001030273.1:c.177C>G, NM_001030272.3:c.306C>G, NM_001030272.2:c.306C>G, NM_001030272.1:c.306C>G, NR_147789.2:n.718C>G, NR_147789.1:n.781C>G, NR_147787.2:n.647C>G, NR_147787.1:n.710C>G, NM_001351812.2:c.255C>G, NM_001351812.1:c.255C>G, NR_147790.2:n.718C>G, NR_147790.1:n.781C>G, NR_147791.2:n.718C>G, NR_147791.1:n.781C>G, NR_147788.2:n.702C>G, NR_147788.1:n.765C>G, NM_001351823.2:c.177C>G, NM_001351823.1:c.177C>G, NM_001351808.2:c.177C>G, NM_001351808.1:c.177C>G, NM_001351809.2:c.255C>G, NM_001351809.1:c.255C>G, NM_001351818.2:c.177C>G, NM_001351818.1:c.177C>G, NM_001351820.2:c.177C>G, NM_001351820.1:c.177C>G, NR_147785.2:n.647C>G, NR_147785.1:n.710C>G, NR_147786.2:n.647C>G, NR_147786.1:n.710C>G, NM_001351813.2:c.177C>G, NM_001351813.1:c.177C>G, NM_001351816.2:c.177C>G, NM_001351816.1:c.177C>G, NM_001351814.2:c.306C>G, NM_001351814.1:c.306C>G, NM_001297724.2:c.177C>G, NM_001297724.1:c.177C>G, NM_001297719.2:c.306C>G, NM_001297719.1:c.306C>G, NM_001351807.2:c.306C>G, NM_001351807.1:c.306C>G, NM_001351819.2:c.306C>G, NM_001351819.1:c.306C>G, NM_001351821.2:c.177C>G, NM_001351821.1:c.177C>G, NM_001297722.2:c.306C>G, NM_001297722.1:c.306C>G, NM_001351811.2:c.-366C>G, NM_001351811.1:c.-366C>G, NM_001351805.2:c.267C>G, NM_001351805.1:c.267C>G, NM_001351806.2:c.267C>G, NM_001351806.1:c.267C>G, NM_001351822.2:c.177C>G, NM_001351822.1:c.177C>G, XM_011520109.2:c.306C>G, XM_011520109.1:c.306C>G, XM_017017741.2:c.306C>G, XM_017017741.1:c.306C>G, NM_001351824.2:c.306C>G, NM_001351824.1:c.306C>G, NM_001351815.2:c.306C>G, NM_001351815.1:c.306C>G, NM_001351810.2:c.306C>G, NM_001351810.1:c.306C>G, NM_001351817.2:c.306C>G, NM_001351817.1:c.306C>G, XM_047426956.1:c.306C>G, NM_001351804.1:c.306C>G, XM_024448522.1:c.255C>G, XM_047426953.1:c.306C>G, XM_047426955.1:c.306C>G, XM_047426952.1:c.306C>G, XM_047426954.1:c.306C>G, XM_047426957.1:c.435C>G, XM_047426958.1:c.435C>G, NP_001169.3:p.Cys102Trp, XP_011518407.2:p.Cys145Trp, XP_011518409.2:p.Cys145Trp, XP_016873227.1:p.Cys145Trp, XP_016873228.1:p.Cys145Trp, NP_001025444.1:p.Cys59Trp, NP_001025443.1:p.Cys102Trp, NP_001338741.1:p.Cys85Trp, NP_001338752.1:p.Cys59Trp, NP_001338737.1:p.Cys59Trp, NP_001338738.1:p.Cys85Trp, NP_001338747.1:p.Cys59Trp, NP_001338749.1:p.Cys59Trp, NP_001338742.1:p.Cys59Trp, NP_001338745.1:p.Cys59Trp, NP_001338743.1:p.Cys102Trp, NP_001284653.1:p.Cys59Trp, NP_001284648.1:p.Cys102Trp, NP_001338736.1:p.Cys102Trp, NP_001338748.1:p.Cys102Trp, NP_001338750.1:p.Cys59Trp, NP_001284651.1:p.Cys102Trp, NP_001338734.1:p.Cys89Trp, NP_001338735.1:p.Cys89Trp, NP_001338751.1:p.Cys59Trp, XP_011518411.1:p.Cys102Trp, XP_016873230.1:p.Cys102Trp, NP_001338753.1:p.Cys102Trp, NP_001338744.1:p.Cys102Trp, NP_001338739.1:p.Cys102Trp, NP_001338746.1:p.Cys102Trp, XP_047282912.1:p.Cys102Trp, NP_001338733.1:p.Cys102Trp, XP_024304290.1:p.Cys85Trp, XP_047282909.1:p.Cys102Trp, XP_047282911.1:p.Cys102Trp, XP_047282908.1:p.Cys102Trp, XP_047282910.1:p.Cys102Trp, XP_047282913.1:p.Cys145Trp, XP_047282914.1:p.Cys145Trp

          5.

          rs1480267514 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>T [Show Flanks]
            Chromosome:
            11:13365535 (GRCh38)
            11:13387082 (GRCh37)
            Canonical SPDI:
            NC_000011.10:13365534:C:T
            Gene:
            ARNTL (Varview)
            Functional Consequence:
            5_prime_UTR_variant,synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            T=0.0002/1 (ALFA)
            T=0.0002/1 (Estonian)
            HGVS:
            NC_000011.10:g.13365535C>T, NC_000011.9:g.13387082C>T, NM_001178.6:c.495C>T, NM_001178.5:c.495C>T, NM_001178.4:c.495C>T, XM_011520105.4:c.624C>T, XM_011520105.3:c.624C>T, XM_011520105.2:c.624C>T, XM_011520105.1:c.495C>T, XM_011520107.4:c.624C>T, XM_011520107.3:c.624C>T, XM_011520107.2:c.624C>T, XM_011520107.1:c.495C>T, XM_017017738.3:c.624C>T, XM_017017738.2:c.624C>T, XM_017017738.1:c.624C>T, XM_017017739.3:c.624C>T, XM_017017739.2:c.624C>T, XM_017017739.1:c.624C>T, NM_001030273.3:c.366C>T, NM_001030273.2:c.366C>T, NM_001030273.1:c.366C>T, NM_001030272.3:c.495C>T, NM_001030272.2:c.495C>T, NM_001030272.1:c.495C>T, NR_147789.2:n.907C>T, NR_147789.1:n.970C>T, NR_147787.2:n.836C>T, NR_147787.1:n.899C>T, NM_001351812.2:c.444C>T, NM_001351812.1:c.444C>T, NR_147790.2:n.907C>T, NR_147790.1:n.970C>T, NR_147791.2:n.907C>T, NR_147791.1:n.970C>T, NR_147788.2:n.891C>T, NR_147788.1:n.954C>T, NM_001351823.2:c.366C>T, NM_001351823.1:c.366C>T, NM_001351808.2:c.366C>T, NM_001351808.1:c.366C>T, NM_001351809.2:c.444C>T, NM_001351809.1:c.444C>T, NM_001351818.2:c.366C>T, NM_001351818.1:c.366C>T, NM_001351820.2:c.366C>T, NM_001351820.1:c.366C>T, NR_147785.2:n.836C>T, NR_147785.1:n.899C>T, NR_147786.2:n.836C>T, NR_147786.1:n.899C>T, NM_001351813.2:c.366C>T, NM_001351813.1:c.366C>T, NM_001351816.2:c.366C>T, NM_001351816.1:c.366C>T, NM_001351814.2:c.495C>T, NM_001351814.1:c.495C>T, NM_001297724.2:c.366C>T, NM_001297724.1:c.366C>T, NM_001297719.2:c.495C>T, NM_001297719.1:c.495C>T, NM_001351807.2:c.495C>T, NM_001351807.1:c.495C>T, NM_001351819.2:c.495C>T, NM_001351819.1:c.495C>T, NM_001351821.2:c.366C>T, NM_001351821.1:c.366C>T, NM_001297722.2:c.495C>T, NM_001297722.1:c.495C>T, NM_001351811.2:c.-177C>T, NM_001351811.1:c.-177C>T, NM_001351805.2:c.456C>T, NM_001351805.1:c.456C>T, NM_001351806.2:c.456C>T, NM_001351806.1:c.456C>T, NM_001351822.2:c.366C>T, NM_001351822.1:c.366C>T, XM_011520109.2:c.495C>T, XM_011520109.1:c.495C>T, XM_017017741.2:c.495C>T, XM_017017741.1:c.495C>T, NM_001351824.2:c.495C>T, NM_001351824.1:c.495C>T, NM_001351815.2:c.495C>T, NM_001351815.1:c.495C>T, NM_001351810.2:c.495C>T, NM_001351810.1:c.495C>T, NM_001351817.2:c.495C>T, NM_001351817.1:c.495C>T, XM_047426956.1:c.495C>T, NM_001351804.1:c.495C>T, XM_024448522.1:c.444C>T, XM_047426953.1:c.495C>T, XM_047426955.1:c.495C>T, XM_047426952.1:c.495C>T, XM_047426954.1:c.495C>T, XM_047426957.1:c.624C>T, XM_047426958.1:c.624C>T

            6.

            rs1479720523 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>G,T [Show Flanks]
              Chromosome:
              11:13378342 (GRCh38)
              11:13399889 (GRCh37)
              Canonical SPDI:
              NC_000011.10:13378341:C:G,NC_000011.10:13378341:C:T
              Gene:
              ARNTL (Varview)
              Functional Consequence:
              synonymous_variant,non_coding_transcript_variant,genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              G=0./0 (ALFA)
              G=0.000004/1 (TOPMED)
              G=0.000007/1 (GnomAD)
              T=0.000342/1 (KOREAN)
              HGVS:
              NC_000011.10:g.13378342C>G, NC_000011.10:g.13378342C>T, NC_000011.9:g.13399889C>G, NC_000011.9:g.13399889C>T, NM_001178.6:c.1417C>G, NM_001178.6:c.1417C>T, NM_001178.5:c.1417C>G, NM_001178.5:c.1417C>T, NM_001178.4:c.1417C>G, NM_001178.4:c.1417C>T, XM_011520105.4:c.1561C>G, XM_011520105.4:c.1561C>T, XM_011520105.3:c.1561C>G, XM_011520105.3:c.1561C>T, XM_011520105.2:c.1561C>G, XM_011520105.2:c.1561C>T, XM_011520105.1:c.1432C>G, XM_011520105.1:c.1432C>T, XM_011520107.4:c.1546C>G, XM_011520107.4:c.1546C>T, XM_011520107.3:c.1546C>G, XM_011520107.3:c.1546C>T, XM_011520107.2:c.1546C>G, XM_011520107.2:c.1546C>T, XM_011520107.1:c.1417C>G, XM_011520107.1:c.1417C>T, XM_017017738.3:c.1564C>G, XM_017017738.3:c.1564C>T, XM_017017738.2:c.1564C>G, XM_017017738.2:c.1564C>T, XM_017017738.1:c.1564C>G, XM_017017738.1:c.1564C>T, XM_017017739.3:c.1549C>G, XM_017017739.3:c.1549C>T, XM_017017739.2:c.1549C>G, XM_017017739.2:c.1549C>T, XM_017017739.1:c.1549C>G, XM_017017739.1:c.1549C>T, NM_001030273.3:c.1288C>G, NM_001030273.3:c.1288C>T, NM_001030273.2:c.1288C>G, NM_001030273.2:c.1288C>T, NM_001030273.1:c.1288C>G, NM_001030273.1:c.1288C>T, NM_001030272.3:c.1417C>G, NM_001030272.3:c.1417C>T, NM_001030272.2:c.1417C>G, NM_001030272.2:c.1417C>T, NM_001030272.1:c.1417C>G, NM_001030272.1:c.1417C>T, NR_147789.2:n.1829C>G, NR_147789.2:n.1829C>T, NR_147789.1:n.1892C>G, NR_147789.1:n.1892C>T, NR_147787.2:n.1761C>G, NR_147787.2:n.1761C>T, NR_147787.1:n.1824C>G, NR_147787.1:n.1824C>T, NM_001351812.2:c.1369C>G, NM_001351812.2:c.1369C>T, NM_001351812.1:c.1369C>G, NM_001351812.1:c.1369C>T, NR_147790.2:n.1927C>G, NR_147790.2:n.1927C>T, NR_147790.1:n.1990C>G, NR_147790.1:n.1990C>T, NR_147791.2:n.1924C>G, NR_147791.2:n.1924C>T, NR_147791.1:n.1987C>G, NR_147791.1:n.1987C>T, NR_147788.2:n.1908C>G, NR_147788.2:n.1908C>T, NR_147788.1:n.1971C>G, NR_147788.1:n.1971C>T, NM_001351823.2:c.1306C>G, NM_001351823.2:c.1306C>T, NM_001351823.1:c.1306C>G, NM_001351823.1:c.1306C>T, NM_001351808.2:c.1291C>G, NM_001351808.2:c.1291C>T, NM_001351808.1:c.1291C>G, NM_001351808.1:c.1291C>T, NM_001351809.2:c.1369C>G, NM_001351809.2:c.1369C>T, NM_001351809.1:c.1369C>G, NM_001351809.1:c.1369C>T, NM_001351818.2:c.1288C>G, NM_001351818.2:c.1288C>T, NM_001351818.1:c.1288C>G, NM_001351818.1:c.1288C>T, NM_001351820.2:c.1291C>G, NM_001351820.2:c.1291C>T, NM_001351820.1:c.1291C>G, NM_001351820.1:c.1291C>T, NR_147785.2:n.1856C>G, NR_147785.2:n.1856C>T, NR_147785.1:n.1919C>G, NR_147785.1:n.1919C>T, NR_147786.2:n.1853C>G, NR_147786.2:n.1853C>T, NR_147786.1:n.1916C>G, NR_147786.1:n.1916C>T, NM_001351813.2:c.1303C>G, NM_001351813.2:c.1303C>T, NM_001351813.1:c.1303C>G, NM_001351813.1:c.1303C>T, NM_001351816.2:c.1291C>G, NM_001351816.2:c.1291C>T, NM_001351816.1:c.1291C>G, NM_001351816.1:c.1291C>T, NM_001351814.2:c.1435C>G, NM_001351814.2:c.1435C>T, NM_001351814.1:c.1435C>G, NM_001351814.1:c.1435C>T, NM_001297724.2:c.1291C>G, NM_001297724.2:c.1291C>T, NM_001297724.1:c.1291C>G, NM_001297724.1:c.1291C>T, NM_001297719.2:c.1420C>G, NM_001297719.2:c.1420C>T, NM_001297719.1:c.1420C>G, NM_001297719.1:c.1420C>T, NM_001351807.2:c.1435C>G, NM_001351807.2:c.1435C>T, NM_001351807.1:c.1435C>G, NM_001351807.1:c.1435C>T, NM_001351819.2:c.1432C>G, NM_001351819.2:c.1432C>T, NM_001351819.1:c.1432C>G, NM_001351819.1:c.1432C>T, NM_001351821.2:c.1291C>G, NM_001351821.2:c.1291C>T, NM_001351821.1:c.1291C>G, NM_001351821.1:c.1291C>T, NM_001297722.2:c.1420C>G, NM_001297722.2:c.1420C>T, NM_001297722.1:c.1420C>G, NM_001297722.1:c.1420C>T, NM_001351811.2:c.670C>G, NM_001351811.2:c.670C>T, NM_001351811.1:c.670C>G, NM_001351811.1:c.670C>T, NM_001351805.2:c.1381C>G, NM_001351805.2:c.1381C>T, NM_001351805.1:c.1381C>G, NM_001351805.1:c.1381C>T, NM_001351806.2:c.1378C>G, NM_001351806.2:c.1378C>T, NM_001351806.1:c.1378C>G, NM_001351806.1:c.1378C>T, NM_001351822.2:c.1291C>G, NM_001351822.2:c.1291C>T, NM_001351822.1:c.1291C>G, NM_001351822.1:c.1291C>T, XM_011520109.2:c.1435C>G, XM_011520109.2:c.1435C>T, XM_011520109.1:c.1435C>G, XM_011520109.1:c.1435C>T, XM_017017741.2:c.1432C>G, XM_017017741.2:c.1432C>T, XM_017017741.1:c.1432C>G, XM_017017741.1:c.1432C>T, NM_001351824.2:c.1420C>G, NM_001351824.2:c.1420C>T, NM_001351824.1:c.1420C>G, NM_001351824.1:c.1420C>T, NM_001351815.2:c.1417C>G, NM_001351815.2:c.1417C>T, NM_001351815.1:c.1417C>G, NM_001351815.1:c.1417C>T, NM_001351810.2:c.1066C>G, NM_001351810.2:c.1066C>T, NM_001351810.1:c.1066C>G, NM_001351810.1:c.1066C>T, NM_001351817.2:c.1066C>G, NM_001351817.2:c.1066C>T, NM_001351817.1:c.1066C>G, NM_001351817.1:c.1066C>T, XM_047426956.1:c.1435C>G, XM_047426956.1:c.1435C>T, NM_001351804.1:c.1417C>G, NM_001351804.1:c.1417C>T, XM_024448522.1:c.1369C>G, XM_024448522.1:c.1369C>T, XM_047426953.1:c.1435C>G, XM_047426953.1:c.1435C>T, XM_047426955.1:c.1435C>G, XM_047426955.1:c.1435C>T, XM_047426952.1:c.1435C>G, XM_047426952.1:c.1435C>T, XM_047426954.1:c.1435C>G, XM_047426954.1:c.1435C>T, XM_047426957.1:c.1644C>G, XM_047426957.1:c.1644C>T, NP_001169.3:p.Pro473Ala, NP_001169.3:p.Pro473Ser, XP_011518407.2:p.Pro521Ala, XP_011518407.2:p.Pro521Ser, XP_011518409.2:p.Pro516Ala, XP_011518409.2:p.Pro516Ser, XP_016873227.1:p.Pro522Ala, XP_016873227.1:p.Pro522Ser, XP_016873228.1:p.Pro517Ala, XP_016873228.1:p.Pro517Ser, NP_001025444.1:p.Pro430Ala, NP_001025444.1:p.Pro430Ser, NP_001025443.1:p.Pro473Ala, NP_001025443.1:p.Pro473Ser, NP_001338741.1:p.Pro457Ala, NP_001338741.1:p.Pro457Ser, NP_001338752.1:p.Pro436Ala, NP_001338752.1:p.Pro436Ser, NP_001338737.1:p.Pro431Ala, NP_001338737.1:p.Pro431Ser, NP_001338738.1:p.Pro457Ala, NP_001338738.1:p.Pro457Ser, NP_001338747.1:p.Pro430Ala, NP_001338747.1:p.Pro430Ser, NP_001338749.1:p.Pro431Ala, NP_001338749.1:p.Pro431Ser, NP_001338742.1:p.Pro435Ala, NP_001338742.1:p.Pro435Ser, NP_001338745.1:p.Pro431Ala, NP_001338745.1:p.Pro431Ser, NP_001338743.1:p.Pro479Ala, NP_001338743.1:p.Pro479Ser, NP_001284653.1:p.Pro431Ala, NP_001284653.1:p.Pro431Ser, NP_001284648.1:p.Pro474Ala, NP_001284648.1:p.Pro474Ser, NP_001338736.1:p.Pro479Ala, NP_001338736.1:p.Pro479Ser, NP_001338748.1:p.Pro478Ala, NP_001338748.1:p.Pro478Ser, NP_001338750.1:p.Pro431Ala, NP_001338750.1:p.Pro431Ser, NP_001284651.1:p.Pro474Ala, NP_001284651.1:p.Pro474Ser, NP_001338740.1:p.Pro224Ala, NP_001338740.1:p.Pro224Ser, NP_001338734.1:p.Pro461Ala, NP_001338734.1:p.Pro461Ser, NP_001338735.1:p.Pro460Ala, NP_001338735.1:p.Pro460Ser, NP_001338751.1:p.Pro431Ala, NP_001338751.1:p.Pro431Ser, XP_011518411.1:p.Pro479Ala, XP_011518411.1:p.Pro479Ser, XP_016873230.1:p.Pro478Ala, XP_016873230.1:p.Pro478Ser, NP_001338753.1:p.Pro474Ala, NP_001338753.1:p.Pro474Ser, NP_001338744.1:p.Pro473Ala, NP_001338744.1:p.Pro473Ser, NP_001338739.1:p.Pro356Ala, NP_001338739.1:p.Pro356Ser, NP_001338746.1:p.Pro356Ala, NP_001338746.1:p.Pro356Ser, XP_047282912.1:p.Pro479Ala, XP_047282912.1:p.Pro479Ser, NP_001338733.1:p.Pro473Ala, NP_001338733.1:p.Pro473Ser, XP_024304290.1:p.Pro457Ala, XP_024304290.1:p.Pro457Ser, XP_047282909.1:p.Pro479Ala, XP_047282909.1:p.Pro479Ser, XP_047282911.1:p.Pro479Ala, XP_047282911.1:p.Pro479Ser, XP_047282908.1:p.Pro479Ala, XP_047282908.1:p.Pro479Ser, XP_047282910.1:p.Pro479Ala, XP_047282910.1:p.Pro479Ser

              7.

              rs1474506574 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>A [Show Flanks]
                Chromosome:
                11:13374156 (GRCh38)
                11:13395703 (GRCh37)
                Canonical SPDI:
                NC_000011.10:13374155:T:A
                Gene:
                ARNTL (Varview)
                Functional Consequence:
                intron_variant,non_coding_transcript_variant,genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                A=0./0 (ALFA)
                A=0.000007/1 (GnomAD)
                HGVS:
                NC_000011.10:g.13374156T>A, NC_000011.9:g.13395703T>A, NM_001178.6:c.1126T>A, NM_001178.5:c.1126T>A, NM_001178.4:c.1126T>A, XM_011520105.4:c.1255T>A, XM_011520105.3:c.1255T>A, XM_011520105.2:c.1255T>A, XM_011520105.1:c.1126T>A, XM_011520107.4:c.1255T>A, XM_011520107.3:c.1255T>A, XM_011520107.2:c.1255T>A, XM_011520107.1:c.1126T>A, XM_017017738.3:c.1258T>A, XM_017017738.2:c.1258T>A, XM_017017738.1:c.1258T>A, XM_017017739.3:c.1258T>A, XM_017017739.2:c.1258T>A, XM_017017739.1:c.1258T>A, NM_001030273.3:c.997T>A, NM_001030273.2:c.997T>A, NM_001030273.1:c.997T>A, NM_001030272.3:c.1126T>A, NM_001030272.2:c.1126T>A, NM_001030272.1:c.1126T>A, NR_147789.2:n.1538T>A, NR_147789.1:n.1601T>A, NR_147787.2:n.1470T>A, NR_147787.1:n.1533T>A, NM_001351812.2:c.1078T>A, NM_001351812.1:c.1078T>A, NR_147790.2:n.1541T>A, NR_147790.1:n.1604T>A, NR_147791.2:n.1538T>A, NR_147791.1:n.1601T>A, NR_147788.2:n.1522T>A, NR_147788.1:n.1585T>A, NM_001351823.2:c.1000T>A, NM_001351823.1:c.1000T>A, NM_001351808.2:c.1000T>A, NM_001351808.1:c.1000T>A, NM_001351809.2:c.1078T>A, NM_001351809.1:c.1078T>A, NM_001351818.2:c.997T>A, NM_001351818.1:c.997T>A, NM_001351820.2:c.1000T>A, NM_001351820.1:c.1000T>A, NR_147785.2:n.1470T>A, NR_147785.1:n.1533T>A, NR_147786.2:n.1467T>A, NR_147786.1:n.1530T>A, NM_001351813.2:c.997T>A, NM_001351813.1:c.997T>A, NM_001351816.2:c.1000T>A, NM_001351816.1:c.1000T>A, NM_001351814.2:c.1129T>A, NM_001351814.1:c.1129T>A, NM_001297724.2:c.1000T>A, NM_001297724.1:c.1000T>A, NM_001297719.2:c.1129T>A, NM_001297719.1:c.1129T>A, NM_001351807.2:c.1129T>A, NM_001351807.1:c.1129T>A, NM_001351819.2:c.1126T>A, NM_001351819.1:c.1126T>A, NM_001351821.2:c.1000T>A, NM_001351821.1:c.1000T>A, NM_001297722.2:c.1129T>A, NM_001297722.1:c.1129T>A, NM_001351811.2:c.379T>A, NM_001351811.1:c.379T>A, NM_001351805.2:c.1090T>A, NM_001351805.1:c.1090T>A, NM_001351806.2:c.1087T>A, NM_001351806.1:c.1087T>A, NM_001351822.2:c.1000T>A, NM_001351822.1:c.1000T>A, XM_011520109.2:c.1129T>A, XM_011520109.1:c.1129T>A, XM_017017741.2:c.1126T>A, XM_017017741.1:c.1126T>A, NM_001351824.2:c.1129T>A, NM_001351824.1:c.1129T>A, NM_001351815.2:c.1126T>A, NM_001351815.1:c.1126T>A, XM_047426956.1:c.1129T>A, NM_001351804.1:c.1126T>A, XM_024448522.1:c.1078T>A, XM_047426953.1:c.1129T>A, XM_047426955.1:c.1129T>A, XM_047426952.1:c.1129T>A, XM_047426954.1:c.1129T>A, XM_047426957.1:c.1258T>A, NP_001169.3:p.Phe376Ile, XP_011518407.2:p.Phe419Ile, XP_011518409.2:p.Phe419Ile, XP_016873227.1:p.Phe420Ile, XP_016873228.1:p.Phe420Ile, NP_001025444.1:p.Phe333Ile, NP_001025443.1:p.Phe376Ile, NP_001338741.1:p.Phe360Ile, NP_001338752.1:p.Phe334Ile, NP_001338737.1:p.Phe334Ile, NP_001338738.1:p.Phe360Ile, NP_001338747.1:p.Phe333Ile, NP_001338749.1:p.Phe334Ile, NP_001338742.1:p.Phe333Ile, NP_001338745.1:p.Phe334Ile, NP_001338743.1:p.Phe377Ile, NP_001284653.1:p.Phe334Ile, NP_001284648.1:p.Phe377Ile, NP_001338736.1:p.Phe377Ile, NP_001338748.1:p.Phe376Ile, NP_001338750.1:p.Phe334Ile, NP_001284651.1:p.Phe377Ile, NP_001338740.1:p.Phe127Ile, NP_001338734.1:p.Phe364Ile, NP_001338735.1:p.Phe363Ile, NP_001338751.1:p.Phe334Ile, XP_011518411.1:p.Phe377Ile, XP_016873230.1:p.Phe376Ile, NP_001338753.1:p.Phe377Ile, NP_001338744.1:p.Phe376Ile, XP_047282912.1:p.Phe377Ile, NP_001338733.1:p.Phe376Ile, XP_024304290.1:p.Phe360Ile, XP_047282909.1:p.Phe377Ile, XP_047282911.1:p.Phe377Ile, XP_047282908.1:p.Phe377Ile, XP_047282910.1:p.Phe377Ile, XP_047282913.1:p.Phe420Ile

                8.

                rs1471310121 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>C,G [Show Flanks]
                  Chromosome:
                  11:13375632 (GRCh38)
                  11:13397179 (GRCh37)
                  Canonical SPDI:
                  NC_000011.10:13375631:A:C,NC_000011.10:13375631:A:G
                  Gene:
                  ARNTL (Varview)
                  Functional Consequence:
                  missense_variant,coding_sequence_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0./0 (ALFA)
                  C=0.000014/2 (GnomAD)
                  HGVS:
                  NC_000011.10:g.13375632A>C, NC_000011.10:g.13375632A>G, NC_000011.9:g.13397179A>C, NC_000011.9:g.13397179A>G, NM_001178.6:c.1192A>C, NM_001178.6:c.1192A>G, NM_001178.5:c.1192A>C, NM_001178.5:c.1192A>G, NM_001178.4:c.1192A>C, NM_001178.4:c.1192A>G, XM_011520105.4:c.1321A>C, XM_011520105.4:c.1321A>G, XM_011520105.3:c.1321A>C, XM_011520105.3:c.1321A>G, XM_011520105.2:c.1321A>C, XM_011520105.2:c.1321A>G, XM_011520105.1:c.1192A>C, XM_011520105.1:c.1192A>G, XM_011520107.4:c.1321A>C, XM_011520107.4:c.1321A>G, XM_011520107.3:c.1321A>C, XM_011520107.3:c.1321A>G, XM_011520107.2:c.1321A>C, XM_011520107.2:c.1321A>G, XM_011520107.1:c.1192A>C, XM_011520107.1:c.1192A>G, XM_017017738.3:c.1324A>C, XM_017017738.3:c.1324A>G, XM_017017738.2:c.1324A>C, XM_017017738.2:c.1324A>G, XM_017017738.1:c.1324A>C, XM_017017738.1:c.1324A>G, XM_017017739.3:c.1324A>C, XM_017017739.3:c.1324A>G, XM_017017739.2:c.1324A>C, XM_017017739.2:c.1324A>G, XM_017017739.1:c.1324A>C, XM_017017739.1:c.1324A>G, NM_001030273.3:c.1063A>C, NM_001030273.3:c.1063A>G, NM_001030273.2:c.1063A>C, NM_001030273.2:c.1063A>G, NM_001030273.1:c.1063A>C, NM_001030273.1:c.1063A>G, NM_001030272.3:c.1192A>C, NM_001030272.3:c.1192A>G, NM_001030272.2:c.1192A>C, NM_001030272.2:c.1192A>G, NM_001030272.1:c.1192A>C, NM_001030272.1:c.1192A>G, NR_147789.2:n.1604A>C, NR_147789.2:n.1604A>G, NR_147789.1:n.1667A>C, NR_147789.1:n.1667A>G, NR_147787.2:n.1536A>C, NR_147787.2:n.1536A>G, NR_147787.1:n.1599A>C, NR_147787.1:n.1599A>G, NM_001351812.2:c.1144A>C, NM_001351812.2:c.1144A>G, NM_001351812.1:c.1144A>C, NM_001351812.1:c.1144A>G, NR_147790.2:n.1607A>C, NR_147790.2:n.1607A>G, NR_147790.1:n.1670A>C, NR_147790.1:n.1670A>G, NR_147791.2:n.1604A>C, NR_147791.2:n.1604A>G, NR_147791.1:n.1667A>C, NR_147791.1:n.1667A>G, NR_147788.2:n.1588A>C, NR_147788.2:n.1588A>G, NR_147788.1:n.1651A>C, NR_147788.1:n.1651A>G, NM_001351823.2:c.1066A>C, NM_001351823.2:c.1066A>G, NM_001351823.1:c.1066A>C, NM_001351823.1:c.1066A>G, NM_001351808.2:c.1066A>C, NM_001351808.2:c.1066A>G, NM_001351808.1:c.1066A>C, NM_001351808.1:c.1066A>G, NM_001351809.2:c.1144A>C, NM_001351809.2:c.1144A>G, NM_001351809.1:c.1144A>C, NM_001351809.1:c.1144A>G, NM_001351818.2:c.1063A>C, NM_001351818.2:c.1063A>G, NM_001351818.1:c.1063A>C, NM_001351818.1:c.1063A>G, NM_001351820.2:c.1066A>C, NM_001351820.2:c.1066A>G, NM_001351820.1:c.1066A>C, NM_001351820.1:c.1066A>G, NR_147785.2:n.1536A>C, NR_147785.2:n.1536A>G, NR_147785.1:n.1599A>C, NR_147785.1:n.1599A>G, NR_147786.2:n.1533A>C, NR_147786.2:n.1533A>G, NR_147786.1:n.1596A>C, NR_147786.1:n.1596A>G, NM_001351813.2:c.1063A>C, NM_001351813.2:c.1063A>G, NM_001351813.1:c.1063A>C, NM_001351813.1:c.1063A>G, NM_001351816.2:c.1066A>C, NM_001351816.2:c.1066A>G, NM_001351816.1:c.1066A>C, NM_001351816.1:c.1066A>G, NM_001351814.2:c.1195A>C, NM_001351814.2:c.1195A>G, NM_001351814.1:c.1195A>C, NM_001351814.1:c.1195A>G, NM_001297724.2:c.1066A>C, NM_001297724.2:c.1066A>G, NM_001297724.1:c.1066A>C, NM_001297724.1:c.1066A>G, NM_001297719.2:c.1195A>C, NM_001297719.2:c.1195A>G, NM_001297719.1:c.1195A>C, NM_001297719.1:c.1195A>G, NM_001351807.2:c.1195A>C, NM_001351807.2:c.1195A>G, NM_001351807.1:c.1195A>C, NM_001351807.1:c.1195A>G, NM_001351819.2:c.1192A>C, NM_001351819.2:c.1192A>G, NM_001351819.1:c.1192A>C, NM_001351819.1:c.1192A>G, NM_001351821.2:c.1066A>C, NM_001351821.2:c.1066A>G, NM_001351821.1:c.1066A>C, NM_001351821.1:c.1066A>G, NM_001297722.2:c.1195A>C, NM_001297722.2:c.1195A>G, NM_001297722.1:c.1195A>C, NM_001297722.1:c.1195A>G, NM_001351811.2:c.445A>C, NM_001351811.2:c.445A>G, NM_001351811.1:c.445A>C, NM_001351811.1:c.445A>G, NM_001351805.2:c.1156A>C, NM_001351805.2:c.1156A>G, NM_001351805.1:c.1156A>C, NM_001351805.1:c.1156A>G, NM_001351806.2:c.1153A>C, NM_001351806.2:c.1153A>G, NM_001351806.1:c.1153A>C, NM_001351806.1:c.1153A>G, NM_001351822.2:c.1066A>C, NM_001351822.2:c.1066A>G, NM_001351822.1:c.1066A>C, NM_001351822.1:c.1066A>G, XM_011520109.2:c.1195A>C, XM_011520109.2:c.1195A>G, XM_011520109.1:c.1195A>C, XM_011520109.1:c.1195A>G, XM_017017741.2:c.1192A>C, XM_017017741.2:c.1192A>G, XM_017017741.1:c.1192A>C, XM_017017741.1:c.1192A>G, NM_001351824.2:c.1195A>C, NM_001351824.2:c.1195A>G, NM_001351824.1:c.1195A>C, NM_001351824.1:c.1195A>G, NM_001351815.2:c.1192A>C, NM_001351815.2:c.1192A>G, NM_001351815.1:c.1192A>C, NM_001351815.1:c.1192A>G, NM_001351810.2:c.841A>C, NM_001351810.2:c.841A>G, NM_001351810.1:c.841A>C, NM_001351810.1:c.841A>G, NM_001351817.2:c.841A>C, NM_001351817.2:c.841A>G, NM_001351817.1:c.841A>C, NM_001351817.1:c.841A>G, XM_047426956.1:c.1195A>C, XM_047426956.1:c.1195A>G, NM_001351804.1:c.1192A>C, NM_001351804.1:c.1192A>G, XM_024448522.1:c.1144A>C, XM_024448522.1:c.1144A>G, XM_047426953.1:c.1195A>C, XM_047426953.1:c.1195A>G, XM_047426955.1:c.1195A>C, XM_047426955.1:c.1195A>G, XM_047426952.1:c.1195A>C, XM_047426952.1:c.1195A>G, XM_047426954.1:c.1195A>C, XM_047426954.1:c.1195A>G, XM_047426957.1:c.1324A>C, XM_047426957.1:c.1324A>G, NP_001169.3:p.Ile398Leu, NP_001169.3:p.Ile398Val, XP_011518407.2:p.Ile441Leu, XP_011518407.2:p.Ile441Val, XP_011518409.2:p.Ile441Leu, XP_011518409.2:p.Ile441Val, XP_016873227.1:p.Ile442Leu, XP_016873227.1:p.Ile442Val, XP_016873228.1:p.Ile442Leu, XP_016873228.1:p.Ile442Val, NP_001025444.1:p.Ile355Leu, NP_001025444.1:p.Ile355Val, NP_001025443.1:p.Ile398Leu, NP_001025443.1:p.Ile398Val, NP_001338741.1:p.Ile382Leu, NP_001338741.1:p.Ile382Val, NP_001338752.1:p.Ile356Leu, NP_001338752.1:p.Ile356Val, NP_001338737.1:p.Ile356Leu, NP_001338737.1:p.Ile356Val, NP_001338738.1:p.Ile382Leu, NP_001338738.1:p.Ile382Val, NP_001338747.1:p.Ile355Leu, NP_001338747.1:p.Ile355Val, NP_001338749.1:p.Ile356Leu, NP_001338749.1:p.Ile356Val, NP_001338742.1:p.Ile355Leu, NP_001338742.1:p.Ile355Val, NP_001338745.1:p.Ile356Leu, NP_001338745.1:p.Ile356Val, NP_001338743.1:p.Ile399Leu, NP_001338743.1:p.Ile399Val, NP_001284653.1:p.Ile356Leu, NP_001284653.1:p.Ile356Val, NP_001284648.1:p.Ile399Leu, NP_001284648.1:p.Ile399Val, NP_001338736.1:p.Ile399Leu, NP_001338736.1:p.Ile399Val, NP_001338748.1:p.Ile398Leu, NP_001338748.1:p.Ile398Val, NP_001338750.1:p.Ile356Leu, NP_001338750.1:p.Ile356Val, NP_001284651.1:p.Ile399Leu, NP_001284651.1:p.Ile399Val, NP_001338740.1:p.Ile149Leu, NP_001338740.1:p.Ile149Val, NP_001338734.1:p.Ile386Leu, NP_001338734.1:p.Ile386Val, NP_001338735.1:p.Ile385Leu, NP_001338735.1:p.Ile385Val, NP_001338751.1:p.Ile356Leu, NP_001338751.1:p.Ile356Val, XP_011518411.1:p.Ile399Leu, XP_011518411.1:p.Ile399Val, XP_016873230.1:p.Ile398Leu, XP_016873230.1:p.Ile398Val, NP_001338753.1:p.Ile399Leu, NP_001338753.1:p.Ile399Val, NP_001338744.1:p.Ile398Leu, NP_001338744.1:p.Ile398Val, NP_001338739.1:p.Ile281Leu, NP_001338739.1:p.Ile281Val, NP_001338746.1:p.Ile281Leu, NP_001338746.1:p.Ile281Val, XP_047282912.1:p.Ile399Leu, XP_047282912.1:p.Ile399Val, NP_001338733.1:p.Ile398Leu, NP_001338733.1:p.Ile398Val, XP_024304290.1:p.Ile382Leu, XP_024304290.1:p.Ile382Val, XP_047282909.1:p.Ile399Leu, XP_047282909.1:p.Ile399Val, XP_047282911.1:p.Ile399Leu, XP_047282911.1:p.Ile399Val, XP_047282908.1:p.Ile399Leu, XP_047282908.1:p.Ile399Val, XP_047282910.1:p.Ile399Leu, XP_047282910.1:p.Ile399Val, XP_047282913.1:p.Ile442Leu, XP_047282913.1:p.Ile442Val

                  9.

                  rs1469622122 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>C [Show Flanks]
                    Chromosome:
                    11:13354338 (GRCh38)
                    11:13375885 (GRCh37)
                    Canonical SPDI:
                    NC_000011.10:13354337:A:C
                    Gene:
                    ARNTL (Varview), LOC124902636 (Varview)
                    Functional Consequence:
                    500B_downstream_variant,non_coding_transcript_variant,synonymous_variant,downstream_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    C=0./0 (ALFA)
                    C=0.000007/1 (GnomAD)
                    C=0.000023/6 (TOPMED)
                    HGVS:
                    NC_000011.10:g.13354338A>C, NC_000011.9:g.13375885A>C, NM_001178.6:c.30A>C, NM_001178.5:c.30A>C, NM_001178.4:c.30A>C, XM_011520105.4:c.159A>C, XM_011520105.3:c.159A>C, XM_011520105.2:c.159A>C, XM_011520105.1:c.30A>C, XM_011520107.4:c.159A>C, XM_011520107.3:c.159A>C, XM_011520107.2:c.159A>C, XM_011520107.1:c.30A>C, XM_017017738.3:c.159A>C, XM_017017738.2:c.159A>C, XM_017017738.1:c.159A>C, XM_017017739.3:c.159A>C, XM_017017739.2:c.159A>C, XM_017017739.1:c.159A>C, NM_001030273.3:c.-171A>C, NM_001030273.2:c.-171A>C, NM_001030273.1:c.-171A>C, NM_001030272.3:c.30A>C, NM_001030272.2:c.30A>C, NM_001030272.1:c.30A>C, NR_147789.2:n.371A>C, NR_147789.1:n.434A>C, NR_147787.2:n.371A>C, NR_147787.1:n.434A>C, NM_001351812.2:c.-146A>C, NM_001351812.1:c.-146A>C, NR_147790.2:n.371A>C, NR_147790.1:n.434A>C, NR_147791.2:n.371A>C, NR_147791.1:n.434A>C, NR_147788.2:n.426A>C, NR_147788.1:n.489A>C, NM_001351823.2:c.-171A>C, NM_001351823.1:c.-171A>C, NM_001351808.2:c.-171A>C, NM_001351808.1:c.-171A>C, NM_001351809.2:c.-146A>C, NM_001351809.1:c.-146A>C, NM_001351818.2:c.-171A>C, NM_001351818.1:c.-171A>C, NM_001351820.2:c.-164A>C, NM_001351820.1:c.-164A>C, NR_147785.2:n.371A>C, NR_147785.1:n.434A>C, NR_147786.2:n.371A>C, NR_147786.1:n.434A>C, NM_001351813.2:c.-171A>C, NM_001351813.1:c.-171A>C, NM_001351816.2:c.-171A>C, NM_001351816.1:c.-171A>C, NM_001351814.2:c.30A>C, NM_001351814.1:c.30A>C, NM_001297724.2:c.-164A>C, NM_001297724.1:c.-164A>C, NM_001297719.2:c.30A>C, NM_001297719.1:c.30A>C, NM_001351807.2:c.30A>C, NM_001351807.1:c.30A>C, NM_001351819.2:c.30A>C, NM_001351819.1:c.30A>C, NM_001351821.2:c.-171A>C, NM_001351821.1:c.-171A>C, NM_001297722.2:c.30A>C, NM_001297722.1:c.30A>C, NM_001351811.2:c.-713A>C, NM_001351811.1:c.-713A>C, NM_001351805.2:c.30A>C, NM_001351805.1:c.30A>C, NM_001351806.2:c.30A>C, NM_001351806.1:c.30A>C, NM_001351822.2:c.-171A>C, NM_001351822.1:c.-171A>C, XM_011520109.2:c.30A>C, XM_011520109.1:c.30A>C, XM_017017741.2:c.30A>C, XM_017017741.1:c.30A>C, NM_001351824.2:c.30A>C, NM_001351824.1:c.30A>C, NM_001351815.2:c.30A>C, NM_001351815.1:c.30A>C, NM_001351810.2:c.30A>C, NM_001351810.1:c.30A>C, NM_001351817.2:c.30A>C, NM_001351817.1:c.30A>C, XM_047426956.1:c.30A>C, NM_001351804.1:c.30A>C, XM_047426953.1:c.30A>C, XM_047426955.1:c.30A>C, XM_047426952.1:c.30A>C, XM_047426954.1:c.30A>C, XM_047426957.1:c.159A>C, XM_047426958.1:c.159A>C

                    10.

                    rs1469394014 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      T>C [Show Flanks]
                      Chromosome:
                      11:13376648 (GRCh38)
                      11:13398195 (GRCh37)
                      Canonical SPDI:
                      NC_000011.10:13376647:T:C
                      Gene:
                      ARNTL (Varview)
                      Functional Consequence:
                      coding_sequence_variant,missense_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      C=0./0 (ALFA)
                      C=0.000004/1 (TOPMED)
                      C=0.000008/2 (GnomAD_exomes)
                      HGVS:
                      NC_000011.10:g.13376648T>C, NC_000011.9:g.13398195T>C, NM_001178.6:c.1331T>C, NM_001178.5:c.1331T>C, NM_001178.4:c.1331T>C, XM_011520105.4:c.1460T>C, XM_011520105.3:c.1460T>C, XM_011520105.2:c.1460T>C, XM_011520105.1:c.1331T>C, XM_011520107.4:c.1460T>C, XM_011520107.3:c.1460T>C, XM_011520107.2:c.1460T>C, XM_011520107.1:c.1331T>C, XM_017017738.3:c.1463T>C, XM_017017738.2:c.1463T>C, XM_017017738.1:c.1463T>C, XM_017017739.3:c.1463T>C, XM_017017739.2:c.1463T>C, XM_017017739.1:c.1463T>C, NM_001030273.3:c.1202T>C, NM_001030273.2:c.1202T>C, NM_001030273.1:c.1202T>C, NM_001030272.3:c.1331T>C, NM_001030272.2:c.1331T>C, NM_001030272.1:c.1331T>C, NR_147789.2:n.1743T>C, NR_147789.1:n.1806T>C, NR_147787.2:n.1675T>C, NR_147787.1:n.1738T>C, NM_001351812.2:c.1283T>C, NM_001351812.1:c.1283T>C, NR_147790.2:n.1841T>C, NR_147790.1:n.1904T>C, NR_147791.2:n.1838T>C, NR_147791.1:n.1901T>C, NR_147788.2:n.1822T>C, NR_147788.1:n.1885T>C, NM_001351823.2:c.1205T>C, NM_001351823.1:c.1205T>C, NM_001351808.2:c.1205T>C, NM_001351808.1:c.1205T>C, NM_001351809.2:c.1283T>C, NM_001351809.1:c.1283T>C, NM_001351818.2:c.1202T>C, NM_001351818.1:c.1202T>C, NM_001351820.2:c.1205T>C, NM_001351820.1:c.1205T>C, NR_147785.2:n.1770T>C, NR_147785.1:n.1833T>C, NR_147786.2:n.1767T>C, NR_147786.1:n.1830T>C, NM_001351813.2:c.1202T>C, NM_001351813.1:c.1202T>C, NM_001351816.2:c.1205T>C, NM_001351816.1:c.1205T>C, NM_001351814.2:c.1334T>C, NM_001351814.1:c.1334T>C, NM_001297724.2:c.1205T>C, NM_001297724.1:c.1205T>C, NM_001297719.2:c.1334T>C, NM_001297719.1:c.1334T>C, NM_001351807.2:c.1334T>C, NM_001351807.1:c.1334T>C, NM_001351819.2:c.1331T>C, NM_001351819.1:c.1331T>C, NM_001351821.2:c.1205T>C, NM_001351821.1:c.1205T>C, NM_001297722.2:c.1334T>C, NM_001297722.1:c.1334T>C, NM_001351811.2:c.584T>C, NM_001351811.1:c.584T>C, NM_001351805.2:c.1295T>C, NM_001351805.1:c.1295T>C, NM_001351806.2:c.1292T>C, NM_001351806.1:c.1292T>C, NM_001351822.2:c.1205T>C, NM_001351822.1:c.1205T>C, XM_011520109.2:c.1334T>C, XM_011520109.1:c.1334T>C, XM_017017741.2:c.1331T>C, XM_017017741.1:c.1331T>C, NM_001351824.2:c.1334T>C, NM_001351824.1:c.1334T>C, NM_001351815.2:c.1331T>C, NM_001351815.1:c.1331T>C, NM_001351810.2:c.980T>C, NM_001351810.1:c.980T>C, NM_001351817.2:c.980T>C, NM_001351817.1:c.980T>C, XM_047426956.1:c.1334T>C, NM_001351804.1:c.1331T>C, XM_024448522.1:c.1283T>C, XM_047426953.1:c.1334T>C, XM_047426955.1:c.1334T>C, XM_047426952.1:c.1334T>C, XM_047426954.1:c.1334T>C, XM_047426957.1:c.1558T>C, NP_001169.3:p.Val444Ala, XP_011518407.2:p.Val487Ala, XP_011518409.2:p.Val487Ala, XP_016873227.1:p.Val488Ala, XP_016873228.1:p.Val488Ala, NP_001025444.1:p.Val401Ala, NP_001025443.1:p.Val444Ala, NP_001338741.1:p.Val428Ala, NP_001338752.1:p.Val402Ala, NP_001338737.1:p.Val402Ala, NP_001338738.1:p.Val428Ala, NP_001338747.1:p.Val401Ala, NP_001338749.1:p.Val402Ala, NP_001338742.1:p.Val401Ala, NP_001338745.1:p.Val402Ala, NP_001338743.1:p.Val445Ala, NP_001284653.1:p.Val402Ala, NP_001284648.1:p.Val445Ala, NP_001338736.1:p.Val445Ala, NP_001338748.1:p.Val444Ala, NP_001338750.1:p.Val402Ala, NP_001284651.1:p.Val445Ala, NP_001338740.1:p.Val195Ala, NP_001338734.1:p.Val432Ala, NP_001338735.1:p.Val431Ala, NP_001338751.1:p.Val402Ala, XP_011518411.1:p.Val445Ala, XP_016873230.1:p.Val444Ala, NP_001338753.1:p.Val445Ala, NP_001338744.1:p.Val444Ala, NP_001338739.1:p.Val327Ala, NP_001338746.1:p.Val327Ala, XP_047282912.1:p.Val445Ala, NP_001338733.1:p.Val444Ala, XP_024304290.1:p.Val428Ala, XP_047282909.1:p.Val445Ala, XP_047282911.1:p.Val445Ala, XP_047282908.1:p.Val445Ala, XP_047282910.1:p.Val445Ala, XP_047282913.1:p.Ser520Pro

                      11.

                      rs1467340502 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        A>G [Show Flanks]
                        Chromosome:
                        11:13354316 (GRCh38)
                        11:13375863 (GRCh37)
                        Canonical SPDI:
                        NC_000011.10:13354315:A:G
                        Gene:
                        ARNTL (Varview), LOC124902636 (Varview)
                        Functional Consequence:
                        500B_downstream_variant,missense_variant,non_coding_transcript_variant,downstream_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant
                        Validated:
                        by frequency,by cluster
                        MAF:
                        G=0.000004/1 (GnomAD_exomes)
                        HGVS:
                        NC_000011.10:g.13354316A>G, NC_000011.9:g.13375863A>G, NM_001178.6:c.8A>G, NM_001178.5:c.8A>G, NM_001178.4:c.8A>G, XM_011520105.4:c.137A>G, XM_011520105.3:c.137A>G, XM_011520105.2:c.137A>G, XM_011520105.1:c.8A>G, XM_011520107.4:c.137A>G, XM_011520107.3:c.137A>G, XM_011520107.2:c.137A>G, XM_011520107.1:c.8A>G, XM_017017738.3:c.137A>G, XM_017017738.2:c.137A>G, XM_017017738.1:c.137A>G, XM_017017739.3:c.137A>G, XM_017017739.2:c.137A>G, XM_017017739.1:c.137A>G, NM_001030273.3:c.-193A>G, NM_001030273.2:c.-193A>G, NM_001030273.1:c.-193A>G, NM_001030272.3:c.8A>G, NM_001030272.2:c.8A>G, NM_001030272.1:c.8A>G, NR_147789.2:n.349A>G, NR_147789.1:n.412A>G, NR_147787.2:n.349A>G, NR_147787.1:n.412A>G, NM_001351812.2:c.-168A>G, NM_001351812.1:c.-168A>G, NR_147790.2:n.349A>G, NR_147790.1:n.412A>G, NR_147791.2:n.349A>G, NR_147791.1:n.412A>G, NR_147788.2:n.404A>G, NR_147788.1:n.467A>G, NM_001351823.2:c.-193A>G, NM_001351823.1:c.-193A>G, NM_001351808.2:c.-193A>G, NM_001351808.1:c.-193A>G, NM_001351809.2:c.-168A>G, NM_001351809.1:c.-168A>G, NM_001351818.2:c.-193A>G, NM_001351818.1:c.-193A>G, NM_001351820.2:c.-186A>G, NM_001351820.1:c.-186A>G, NR_147785.2:n.349A>G, NR_147785.1:n.412A>G, NR_147786.2:n.349A>G, NR_147786.1:n.412A>G, NM_001351813.2:c.-193A>G, NM_001351813.1:c.-193A>G, NM_001351816.2:c.-193A>G, NM_001351816.1:c.-193A>G, NM_001351814.2:c.8A>G, NM_001351814.1:c.8A>G, NM_001297724.2:c.-186A>G, NM_001297724.1:c.-186A>G, NM_001297719.2:c.8A>G, NM_001297719.1:c.8A>G, NM_001351807.2:c.8A>G, NM_001351807.1:c.8A>G, NM_001351819.2:c.8A>G, NM_001351819.1:c.8A>G, NM_001351821.2:c.-193A>G, NM_001351821.1:c.-193A>G, NM_001297722.2:c.8A>G, NM_001297722.1:c.8A>G, NM_001351811.2:c.-735A>G, NM_001351811.1:c.-735A>G, NM_001351805.2:c.8A>G, NM_001351805.1:c.8A>G, NM_001351806.2:c.8A>G, NM_001351806.1:c.8A>G, NM_001351822.2:c.-193A>G, NM_001351822.1:c.-193A>G, XM_011520109.2:c.8A>G, XM_011520109.1:c.8A>G, XM_017017741.2:c.8A>G, XM_017017741.1:c.8A>G, NM_001351824.2:c.8A>G, NM_001351824.1:c.8A>G, NM_001351815.2:c.8A>G, NM_001351815.1:c.8A>G, NM_001351810.2:c.8A>G, NM_001351810.1:c.8A>G, NM_001351817.2:c.8A>G, NM_001351817.1:c.8A>G, XM_047426956.1:c.8A>G, NM_001351804.1:c.8A>G, XM_047426953.1:c.8A>G, XM_047426955.1:c.8A>G, XM_047426952.1:c.8A>G, XM_047426954.1:c.8A>G, XM_047426957.1:c.137A>G, XM_047426958.1:c.137A>G, NP_001169.3:p.Asp3Gly, XP_011518407.2:p.Asp46Gly, XP_011518409.2:p.Asp46Gly, XP_016873227.1:p.Asp46Gly, XP_016873228.1:p.Asp46Gly, NP_001025443.1:p.Asp3Gly, NP_001338743.1:p.Asp3Gly, NP_001284648.1:p.Asp3Gly, NP_001338736.1:p.Asp3Gly, NP_001338748.1:p.Asp3Gly, NP_001284651.1:p.Asp3Gly, NP_001338734.1:p.Asp3Gly, NP_001338735.1:p.Asp3Gly, XP_011518411.1:p.Asp3Gly, XP_016873230.1:p.Asp3Gly, NP_001338753.1:p.Asp3Gly, NP_001338744.1:p.Asp3Gly, NP_001338739.1:p.Asp3Gly, NP_001338746.1:p.Asp3Gly, XP_047282912.1:p.Asp3Gly, NP_001338733.1:p.Asp3Gly, XP_047282909.1:p.Asp3Gly, XP_047282911.1:p.Asp3Gly, XP_047282908.1:p.Asp3Gly, XP_047282910.1:p.Asp3Gly, XP_047282913.1:p.Asp46Gly, XP_047282914.1:p.Asp46Gly

                        12.

                        rs1456469487 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          A>G [Show Flanks]
                          Chromosome:
                          11:13360375 (GRCh38)
                          11:13381922 (GRCh37)
                          Canonical SPDI:
                          NC_000011.10:13360374:A:G
                          Gene:
                          ARNTL (Varview), LOC124902636 (Varview)
                          Functional Consequence:
                          missense_variant,non_coding_transcript_variant,2KB_upstream_variant,5_prime_UTR_variant,upstream_transcript_variant,coding_sequence_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          G=0./0 (ALFA)
                          G=0.000004/1 (GnomAD_exomes)
                          G=0.000004/1 (TOPMED)
                          G=0.000007/1 (GnomAD)
                          HGVS:
                          NC_000011.10:g.13360375A>G, NC_000011.9:g.13381922A>G, NM_001178.6:c.410A>G, NM_001178.5:c.410A>G, NM_001178.4:c.410A>G, XM_011520105.4:c.539A>G, XM_011520105.3:c.539A>G, XM_011520105.2:c.539A>G, XM_011520105.1:c.410A>G, XM_011520107.4:c.539A>G, XM_011520107.3:c.539A>G, XM_011520107.2:c.539A>G, XM_011520107.1:c.410A>G, XM_017017738.3:c.539A>G, XM_017017738.2:c.539A>G, XM_017017738.1:c.539A>G, XM_017017739.3:c.539A>G, XM_017017739.2:c.539A>G, XM_017017739.1:c.539A>G, NM_001030273.3:c.281A>G, NM_001030273.2:c.281A>G, NM_001030273.1:c.281A>G, NM_001030272.3:c.410A>G, NM_001030272.2:c.410A>G, NM_001030272.1:c.410A>G, NR_147789.2:n.822A>G, NR_147789.1:n.885A>G, NR_147787.2:n.751A>G, NR_147787.1:n.814A>G, NM_001351812.2:c.359A>G, NM_001351812.1:c.359A>G, NR_147790.2:n.822A>G, NR_147790.1:n.885A>G, NR_147791.2:n.822A>G, NR_147791.1:n.885A>G, NR_147788.2:n.806A>G, NR_147788.1:n.869A>G, NM_001351823.2:c.281A>G, NM_001351823.1:c.281A>G, NM_001351808.2:c.281A>G, NM_001351808.1:c.281A>G, NM_001351809.2:c.359A>G, NM_001351809.1:c.359A>G, NM_001351818.2:c.281A>G, NM_001351818.1:c.281A>G, NM_001351820.2:c.281A>G, NM_001351820.1:c.281A>G, NR_147785.2:n.751A>G, NR_147785.1:n.814A>G, NR_147786.2:n.751A>G, NR_147786.1:n.814A>G, NM_001351813.2:c.281A>G, NM_001351813.1:c.281A>G, NM_001351816.2:c.281A>G, NM_001351816.1:c.281A>G, NM_001351814.2:c.410A>G, NM_001351814.1:c.410A>G, NM_001297724.2:c.281A>G, NM_001297724.1:c.281A>G, NM_001297719.2:c.410A>G, NM_001297719.1:c.410A>G, NM_001351807.2:c.410A>G, NM_001351807.1:c.410A>G, NM_001351819.2:c.410A>G, NM_001351819.1:c.410A>G, NM_001351821.2:c.281A>G, NM_001351821.1:c.281A>G, NM_001297722.2:c.410A>G, NM_001297722.1:c.410A>G, NM_001351811.2:c.-262A>G, NM_001351811.1:c.-262A>G, NM_001351805.2:c.371A>G, NM_001351805.1:c.371A>G, NM_001351806.2:c.371A>G, NM_001351806.1:c.371A>G, NM_001351822.2:c.281A>G, NM_001351822.1:c.281A>G, XM_011520109.2:c.410A>G, XM_011520109.1:c.410A>G, XM_017017741.2:c.410A>G, XM_017017741.1:c.410A>G, NM_001351824.2:c.410A>G, NM_001351824.1:c.410A>G, NM_001351815.2:c.410A>G, NM_001351815.1:c.410A>G, NM_001351810.2:c.410A>G, NM_001351810.1:c.410A>G, NM_001351817.2:c.410A>G, NM_001351817.1:c.410A>G, XM_047426956.1:c.410A>G, NM_001351804.1:c.410A>G, XM_024448522.1:c.359A>G, XM_047426953.1:c.410A>G, XM_047426955.1:c.410A>G, XM_047426952.1:c.410A>G, XM_047426954.1:c.410A>G, XM_047426957.1:c.539A>G, XM_047426958.1:c.539A>G, NP_001169.3:p.Tyr137Cys, XP_011518407.2:p.Tyr180Cys, XP_011518409.2:p.Tyr180Cys, XP_016873227.1:p.Tyr180Cys, XP_016873228.1:p.Tyr180Cys, NP_001025444.1:p.Tyr94Cys, NP_001025443.1:p.Tyr137Cys, NP_001338741.1:p.Tyr120Cys, NP_001338752.1:p.Tyr94Cys, NP_001338737.1:p.Tyr94Cys, NP_001338738.1:p.Tyr120Cys, NP_001338747.1:p.Tyr94Cys, NP_001338749.1:p.Tyr94Cys, NP_001338742.1:p.Tyr94Cys, NP_001338745.1:p.Tyr94Cys, NP_001338743.1:p.Tyr137Cys, NP_001284653.1:p.Tyr94Cys, NP_001284648.1:p.Tyr137Cys, NP_001338736.1:p.Tyr137Cys, NP_001338748.1:p.Tyr137Cys, NP_001338750.1:p.Tyr94Cys, NP_001284651.1:p.Tyr137Cys, NP_001338734.1:p.Tyr124Cys, NP_001338735.1:p.Tyr124Cys, NP_001338751.1:p.Tyr94Cys, XP_011518411.1:p.Tyr137Cys, XP_016873230.1:p.Tyr137Cys, NP_001338753.1:p.Tyr137Cys, NP_001338744.1:p.Tyr137Cys, NP_001338739.1:p.Tyr137Cys, NP_001338746.1:p.Tyr137Cys, XP_047282912.1:p.Tyr137Cys, NP_001338733.1:p.Tyr137Cys, XP_024304290.1:p.Tyr120Cys, XP_047282909.1:p.Tyr137Cys, XP_047282911.1:p.Tyr137Cys, XP_047282908.1:p.Tyr137Cys, XP_047282910.1:p.Tyr137Cys, XP_047282913.1:p.Tyr180Cys, XP_047282914.1:p.Tyr180Cys

                          13.

                          rs1455771390 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>A [Show Flanks]
                            Chromosome:
                            11:13372257 (GRCh38)
                            11:13393804 (GRCh37)
                            Canonical SPDI:
                            NC_000011.10:13372256:C:A
                            Gene:
                            ARNTL (Varview)
                            Functional Consequence:
                            missense_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant,coding_sequence_variant
                            Validated:
                            by frequency
                            MAF:
                            A=0.000004/1 (GnomAD_exomes)
                            HGVS:
                            NC_000011.10:g.13372257C>A, NC_000011.9:g.13393804C>A, NM_001178.6:c.912C>A, NM_001178.5:c.912C>A, NM_001178.4:c.912C>A, XM_011520105.4:c.1041C>A, XM_011520105.3:c.1041C>A, XM_011520105.2:c.1041C>A, XM_011520105.1:c.912C>A, XM_011520107.4:c.1041C>A, XM_011520107.3:c.1041C>A, XM_011520107.2:c.1041C>A, XM_011520107.1:c.912C>A, XM_017017738.3:c.1044C>A, XM_017017738.2:c.1044C>A, XM_017017738.1:c.1044C>A, XM_017017739.3:c.1044C>A, XM_017017739.2:c.1044C>A, XM_017017739.1:c.1044C>A, NM_001030273.3:c.783C>A, NM_001030273.2:c.783C>A, NM_001030273.1:c.783C>A, NM_001030272.3:c.912C>A, NM_001030272.2:c.912C>A, NM_001030272.1:c.912C>A, NR_147789.2:n.1324C>A, NR_147789.1:n.1387C>A, NR_147787.2:n.1256C>A, NR_147787.1:n.1319C>A, NM_001351812.2:c.864C>A, NM_001351812.1:c.864C>A, NR_147790.2:n.1327C>A, NR_147790.1:n.1390C>A, NR_147791.2:n.1324C>A, NR_147791.1:n.1387C>A, NR_147788.2:n.1308C>A, NR_147788.1:n.1371C>A, NM_001351823.2:c.786C>A, NM_001351823.1:c.786C>A, NM_001351808.2:c.786C>A, NM_001351808.1:c.786C>A, NM_001351809.2:c.864C>A, NM_001351809.1:c.864C>A, NM_001351818.2:c.783C>A, NM_001351818.1:c.783C>A, NM_001351820.2:c.786C>A, NM_001351820.1:c.786C>A, NR_147785.2:n.1256C>A, NR_147785.1:n.1319C>A, NR_147786.2:n.1253C>A, NR_147786.1:n.1316C>A, NM_001351813.2:c.783C>A, NM_001351813.1:c.783C>A, NM_001351816.2:c.786C>A, NM_001351816.1:c.786C>A, NM_001351814.2:c.915C>A, NM_001351814.1:c.915C>A, NM_001297724.2:c.786C>A, NM_001297724.1:c.786C>A, NM_001297719.2:c.915C>A, NM_001297719.1:c.915C>A, NM_001351807.2:c.915C>A, NM_001351807.1:c.915C>A, NM_001351819.2:c.912C>A, NM_001351819.1:c.912C>A, NM_001351821.2:c.786C>A, NM_001351821.1:c.786C>A, NM_001297722.2:c.915C>A, NM_001297722.1:c.915C>A, NM_001351811.2:c.165C>A, NM_001351811.1:c.165C>A, NM_001351805.2:c.876C>A, NM_001351805.1:c.876C>A, NM_001351806.2:c.873C>A, NM_001351806.1:c.873C>A, NM_001351822.2:c.786C>A, NM_001351822.1:c.786C>A, XM_011520109.2:c.915C>A, XM_011520109.1:c.915C>A, XM_017017741.2:c.912C>A, XM_017017741.1:c.912C>A, NM_001351824.2:c.915C>A, NM_001351824.1:c.915C>A, NM_001351815.2:c.912C>A, NM_001351815.1:c.912C>A, XM_047426956.1:c.915C>A, NM_001351804.1:c.912C>A, XM_024448522.1:c.864C>A, XM_047426953.1:c.915C>A, XM_047426955.1:c.915C>A, XM_047426952.1:c.915C>A, XM_047426954.1:c.915C>A, XM_047426957.1:c.1044C>A, NP_001169.3:p.Asp304Glu, XP_011518407.2:p.Asp347Glu, XP_011518409.2:p.Asp347Glu, XP_016873227.1:p.Asp348Glu, XP_016873228.1:p.Asp348Glu, NP_001025444.1:p.Asp261Glu, NP_001025443.1:p.Asp304Glu, NP_001338741.1:p.Asp288Glu, NP_001338752.1:p.Asp262Glu, NP_001338737.1:p.Asp262Glu, NP_001338738.1:p.Asp288Glu, NP_001338747.1:p.Asp261Glu, NP_001338749.1:p.Asp262Glu, NP_001338742.1:p.Asp261Glu, NP_001338745.1:p.Asp262Glu, NP_001338743.1:p.Asp305Glu, NP_001284653.1:p.Asp262Glu, NP_001284648.1:p.Asp305Glu, NP_001338736.1:p.Asp305Glu, NP_001338748.1:p.Asp304Glu, NP_001338750.1:p.Asp262Glu, NP_001284651.1:p.Asp305Glu, NP_001338740.1:p.Asp55Glu, NP_001338734.1:p.Asp292Glu, NP_001338735.1:p.Asp291Glu, NP_001338751.1:p.Asp262Glu, XP_011518411.1:p.Asp305Glu, XP_016873230.1:p.Asp304Glu, NP_001338753.1:p.Asp305Glu, NP_001338744.1:p.Asp304Glu, XP_047282912.1:p.Asp305Glu, NP_001338733.1:p.Asp304Glu, XP_024304290.1:p.Asp288Glu, XP_047282909.1:p.Asp305Glu, XP_047282911.1:p.Asp305Glu, XP_047282908.1:p.Asp305Glu, XP_047282910.1:p.Asp305Glu, XP_047282913.1:p.Asp348Glu

                            14.

                            rs1455360668 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C [Show Flanks]
                              Chromosome:
                              11:13372355 (GRCh38)
                              11:13393902 (GRCh37)
                              Canonical SPDI:
                              NC_000011.10:13372354:T:C
                              Gene:
                              ARNTL (Varview)
                              Functional Consequence:
                              intron_variant,missense_variant,coding_sequence_variant,non_coding_transcript_variant,genic_downstream_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              C=0./0 (ALFA)
                              C=0.000004/1 (GnomAD_exomes)
                              C=0.000004/1 (TOPMED)
                              HGVS:
                              NC_000011.10:g.13372355T>C, NC_000011.9:g.13393902T>C, NM_001178.6:c.1010T>C, NM_001178.5:c.1010T>C, NM_001178.4:c.1010T>C, XM_011520105.4:c.1139T>C, XM_011520105.3:c.1139T>C, XM_011520105.2:c.1139T>C, XM_011520105.1:c.1010T>C, XM_011520107.4:c.1139T>C, XM_011520107.3:c.1139T>C, XM_011520107.2:c.1139T>C, XM_011520107.1:c.1010T>C, XM_017017738.3:c.1142T>C, XM_017017738.2:c.1142T>C, XM_017017738.1:c.1142T>C, XM_017017739.3:c.1142T>C, XM_017017739.2:c.1142T>C, XM_017017739.1:c.1142T>C, NM_001030273.3:c.881T>C, NM_001030273.2:c.881T>C, NM_001030273.1:c.881T>C, NM_001030272.3:c.1010T>C, NM_001030272.2:c.1010T>C, NM_001030272.1:c.1010T>C, NR_147789.2:n.1422T>C, NR_147789.1:n.1485T>C, NR_147787.2:n.1354T>C, NR_147787.1:n.1417T>C, NM_001351812.2:c.962T>C, NM_001351812.1:c.962T>C, NR_147790.2:n.1425T>C, NR_147790.1:n.1488T>C, NR_147791.2:n.1422T>C, NR_147791.1:n.1485T>C, NR_147788.2:n.1406T>C, NR_147788.1:n.1469T>C, NM_001351823.2:c.884T>C, NM_001351823.1:c.884T>C, NM_001351808.2:c.884T>C, NM_001351808.1:c.884T>C, NM_001351809.2:c.962T>C, NM_001351809.1:c.962T>C, NM_001351818.2:c.881T>C, NM_001351818.1:c.881T>C, NM_001351820.2:c.884T>C, NM_001351820.1:c.884T>C, NR_147785.2:n.1354T>C, NR_147785.1:n.1417T>C, NR_147786.2:n.1351T>C, NR_147786.1:n.1414T>C, NM_001351813.2:c.881T>C, NM_001351813.1:c.881T>C, NM_001351816.2:c.884T>C, NM_001351816.1:c.884T>C, NM_001351814.2:c.1013T>C, NM_001351814.1:c.1013T>C, NM_001297724.2:c.884T>C, NM_001297724.1:c.884T>C, NM_001297719.2:c.1013T>C, NM_001297719.1:c.1013T>C, NM_001351807.2:c.1013T>C, NM_001351807.1:c.1013T>C, NM_001351819.2:c.1010T>C, NM_001351819.1:c.1010T>C, NM_001351821.2:c.884T>C, NM_001351821.1:c.884T>C, NM_001297722.2:c.1013T>C, NM_001297722.1:c.1013T>C, NM_001351811.2:c.263T>C, NM_001351811.1:c.263T>C, NM_001351805.2:c.974T>C, NM_001351805.1:c.974T>C, NM_001351806.2:c.971T>C, NM_001351806.1:c.971T>C, NM_001351822.2:c.884T>C, NM_001351822.1:c.884T>C, XM_011520109.2:c.1013T>C, XM_011520109.1:c.1013T>C, XM_017017741.2:c.1010T>C, XM_017017741.1:c.1010T>C, NM_001351824.2:c.1013T>C, NM_001351824.1:c.1013T>C, NM_001351815.2:c.1010T>C, NM_001351815.1:c.1010T>C, XM_047426956.1:c.1013T>C, NM_001351804.1:c.1010T>C, XM_024448522.1:c.962T>C, XM_047426953.1:c.1013T>C, XM_047426955.1:c.1013T>C, XM_047426952.1:c.1013T>C, XM_047426954.1:c.1013T>C, XM_047426957.1:c.1142T>C, NP_001169.3:p.Met337Thr, XP_011518407.2:p.Met380Thr, XP_011518409.2:p.Met380Thr, XP_016873227.1:p.Met381Thr, XP_016873228.1:p.Met381Thr, NP_001025444.1:p.Met294Thr, NP_001025443.1:p.Met337Thr, NP_001338741.1:p.Met321Thr, NP_001338752.1:p.Met295Thr, NP_001338737.1:p.Met295Thr, NP_001338738.1:p.Met321Thr, NP_001338747.1:p.Met294Thr, NP_001338749.1:p.Met295Thr, NP_001338742.1:p.Met294Thr, NP_001338745.1:p.Met295Thr, NP_001338743.1:p.Met338Thr, NP_001284653.1:p.Met295Thr, NP_001284648.1:p.Met338Thr, NP_001338736.1:p.Met338Thr, NP_001338748.1:p.Met337Thr, NP_001338750.1:p.Met295Thr, NP_001284651.1:p.Met338Thr, NP_001338740.1:p.Met88Thr, NP_001338734.1:p.Met325Thr, NP_001338735.1:p.Met324Thr, NP_001338751.1:p.Met295Thr, XP_011518411.1:p.Met338Thr, XP_016873230.1:p.Met337Thr, NP_001338753.1:p.Met338Thr, NP_001338744.1:p.Met337Thr, XP_047282912.1:p.Met338Thr, NP_001338733.1:p.Met337Thr, XP_024304290.1:p.Met321Thr, XP_047282909.1:p.Met338Thr, XP_047282911.1:p.Met338Thr, XP_047282908.1:p.Met338Thr, XP_047282910.1:p.Met338Thr, XP_047282913.1:p.Met381Thr

                              15.

                              rs1454271026 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>T [Show Flanks]
                                Chromosome:
                                11:13366733 (GRCh38)
                                11:13388280 (GRCh37)
                                Canonical SPDI:
                                NC_000011.10:13366732:G:T
                                Gene:
                                ARNTL (Varview)
                                Functional Consequence:
                                5_prime_UTR_variant,non_coding_transcript_variant,coding_sequence_variant,missense_variant
                                HGVS:
                                NC_000011.10:g.13366733G>T, NC_000011.9:g.13388280G>T, NM_001178.6:c.621G>T, NM_001178.5:c.621G>T, NM_001178.4:c.621G>T, XM_011520105.4:c.750G>T, XM_011520105.3:c.750G>T, XM_011520105.2:c.750G>T, XM_011520105.1:c.621G>T, XM_011520107.4:c.750G>T, XM_011520107.3:c.750G>T, XM_011520107.2:c.750G>T, XM_011520107.1:c.621G>T, XM_017017738.3:c.750G>T, XM_017017738.2:c.750G>T, XM_017017738.1:c.750G>T, XM_017017739.3:c.750G>T, XM_017017739.2:c.750G>T, XM_017017739.1:c.750G>T, NM_001030273.3:c.492G>T, NM_001030273.2:c.492G>T, NM_001030273.1:c.492G>T, NM_001030272.3:c.621G>T, NM_001030272.2:c.621G>T, NM_001030272.1:c.621G>T, NR_147789.2:n.1033G>T, NR_147789.1:n.1096G>T, NR_147787.2:n.962G>T, NR_147787.1:n.1025G>T, NM_001351812.2:c.570G>T, NM_001351812.1:c.570G>T, NR_147790.2:n.1033G>T, NR_147790.1:n.1096G>T, NR_147791.2:n.1033G>T, NR_147791.1:n.1096G>T, NR_147788.2:n.1017G>T, NR_147788.1:n.1080G>T, NM_001351823.2:c.492G>T, NM_001351823.1:c.492G>T, NM_001351808.2:c.492G>T, NM_001351808.1:c.492G>T, NM_001351809.2:c.570G>T, NM_001351809.1:c.570G>T, NM_001351818.2:c.492G>T, NM_001351818.1:c.492G>T, NM_001351820.2:c.492G>T, NM_001351820.1:c.492G>T, NR_147785.2:n.962G>T, NR_147785.1:n.1025G>T, NR_147786.2:n.962G>T, NR_147786.1:n.1025G>T, NM_001351813.2:c.492G>T, NM_001351813.1:c.492G>T, NM_001351816.2:c.492G>T, NM_001351816.1:c.492G>T, NM_001351814.2:c.621G>T, NM_001351814.1:c.621G>T, NM_001297724.2:c.492G>T, NM_001297724.1:c.492G>T, NM_001297719.2:c.621G>T, NM_001297719.1:c.621G>T, NM_001351807.2:c.621G>T, NM_001351807.1:c.621G>T, NM_001351819.2:c.621G>T, NM_001351819.1:c.621G>T, NM_001351821.2:c.492G>T, NM_001351821.1:c.492G>T, NM_001297722.2:c.621G>T, NM_001297722.1:c.621G>T, NM_001351811.2:c.-51G>T, NM_001351811.1:c.-51G>T, NM_001351805.2:c.582G>T, NM_001351805.1:c.582G>T, NM_001351806.2:c.582G>T, NM_001351806.1:c.582G>T, NM_001351822.2:c.492G>T, NM_001351822.1:c.492G>T, XM_011520109.2:c.621G>T, XM_011520109.1:c.621G>T, XM_017017741.2:c.621G>T, XM_017017741.1:c.621G>T, NM_001351824.2:c.621G>T, NM_001351824.1:c.621G>T, NM_001351815.2:c.621G>T, NM_001351815.1:c.621G>T, NM_001351810.2:c.621G>T, NM_001351810.1:c.621G>T, NM_001351817.2:c.621G>T, NM_001351817.1:c.621G>T, XM_047426956.1:c.621G>T, NM_001351804.1:c.621G>T, XM_024448522.1:c.570G>T, XM_047426953.1:c.621G>T, XM_047426955.1:c.621G>T, XM_047426952.1:c.621G>T, XM_047426954.1:c.621G>T, XM_047426957.1:c.750G>T, XM_047426958.1:c.750G>T, NP_001169.3:p.Gln207His, XP_011518407.2:p.Gln250His, XP_011518409.2:p.Gln250His, XP_016873227.1:p.Gln250His, XP_016873228.1:p.Gln250His, NP_001025444.1:p.Gln164His, NP_001025443.1:p.Gln207His, NP_001338741.1:p.Gln190His, NP_001338752.1:p.Gln164His, NP_001338737.1:p.Gln164His, NP_001338738.1:p.Gln190His, NP_001338747.1:p.Gln164His, NP_001338749.1:p.Gln164His, NP_001338742.1:p.Gln164His, NP_001338745.1:p.Gln164His, NP_001338743.1:p.Gln207His, NP_001284653.1:p.Gln164His, NP_001284648.1:p.Gln207His, NP_001338736.1:p.Gln207His, NP_001338748.1:p.Gln207His, NP_001338750.1:p.Gln164His, NP_001284651.1:p.Gln207His, NP_001338734.1:p.Gln194His, NP_001338735.1:p.Gln194His, NP_001338751.1:p.Gln164His, XP_011518411.1:p.Gln207His, XP_016873230.1:p.Gln207His, NP_001338753.1:p.Gln207His, NP_001338744.1:p.Gln207His, NP_001338739.1:p.Gln207His, NP_001338746.1:p.Gln207His, XP_047282912.1:p.Gln207His, NP_001338733.1:p.Gln207His, XP_024304290.1:p.Gln190His, XP_047282909.1:p.Gln207His, XP_047282911.1:p.Gln207His, XP_047282908.1:p.Gln207His, XP_047282910.1:p.Gln207His, XP_047282913.1:p.Gln250His, XP_047282914.1:p.Gln250His

                                16.

                                rs1453415631 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>C [Show Flanks]
                                  Chromosome:
                                  11:13354327 (GRCh38)
                                  11:13375874 (GRCh37)
                                  Canonical SPDI:
                                  NC_000011.10:13354326:G:C
                                  Gene:
                                  ARNTL (Varview), LOC124902636 (Varview)
                                  Functional Consequence:
                                  non_coding_transcript_variant,genic_upstream_transcript_variant,downstream_transcript_variant,upstream_transcript_variant,missense_variant,coding_sequence_variant,5_prime_UTR_variant,500B_downstream_variant
                                  Validated:
                                  by frequency,by cluster
                                  MAF:
                                  C=0.000004/1 (GnomAD_exomes)
                                  HGVS:
                                  NC_000011.10:g.13354327G>C, NC_000011.9:g.13375874G>C, NM_001178.6:c.19G>C, NM_001178.5:c.19G>C, NM_001178.4:c.19G>C, XM_011520105.4:c.148G>C, XM_011520105.3:c.148G>C, XM_011520105.2:c.148G>C, XM_011520105.1:c.19G>C, XM_011520107.4:c.148G>C, XM_011520107.3:c.148G>C, XM_011520107.2:c.148G>C, XM_011520107.1:c.19G>C, XM_017017738.3:c.148G>C, XM_017017738.2:c.148G>C, XM_017017738.1:c.148G>C, XM_017017739.3:c.148G>C, XM_017017739.2:c.148G>C, XM_017017739.1:c.148G>C, NM_001030273.3:c.-182G>C, NM_001030273.2:c.-182G>C, NM_001030273.1:c.-182G>C, NM_001030272.3:c.19G>C, NM_001030272.2:c.19G>C, NM_001030272.1:c.19G>C, NR_147789.2:n.360G>C, NR_147789.1:n.423G>C, NR_147787.2:n.360G>C, NR_147787.1:n.423G>C, NM_001351812.2:c.-157G>C, NM_001351812.1:c.-157G>C, NR_147790.2:n.360G>C, NR_147790.1:n.423G>C, NR_147791.2:n.360G>C, NR_147791.1:n.423G>C, NR_147788.2:n.415G>C, NR_147788.1:n.478G>C, NM_001351823.2:c.-182G>C, NM_001351823.1:c.-182G>C, NM_001351808.2:c.-182G>C, NM_001351808.1:c.-182G>C, NM_001351809.2:c.-157G>C, NM_001351809.1:c.-157G>C, NM_001351818.2:c.-182G>C, NM_001351818.1:c.-182G>C, NM_001351820.2:c.-175G>C, NM_001351820.1:c.-175G>C, NR_147785.2:n.360G>C, NR_147785.1:n.423G>C, NR_147786.2:n.360G>C, NR_147786.1:n.423G>C, NM_001351813.2:c.-182G>C, NM_001351813.1:c.-182G>C, NM_001351816.2:c.-182G>C, NM_001351816.1:c.-182G>C, NM_001351814.2:c.19G>C, NM_001351814.1:c.19G>C, NM_001297724.2:c.-175G>C, NM_001297724.1:c.-175G>C, NM_001297719.2:c.19G>C, NM_001297719.1:c.19G>C, NM_001351807.2:c.19G>C, NM_001351807.1:c.19G>C, NM_001351819.2:c.19G>C, NM_001351819.1:c.19G>C, NM_001351821.2:c.-182G>C, NM_001351821.1:c.-182G>C, NM_001297722.2:c.19G>C, NM_001297722.1:c.19G>C, NM_001351811.2:c.-724G>C, NM_001351811.1:c.-724G>C, NM_001351805.2:c.19G>C, NM_001351805.1:c.19G>C, NM_001351806.2:c.19G>C, NM_001351806.1:c.19G>C, NM_001351822.2:c.-182G>C, NM_001351822.1:c.-182G>C, XM_011520109.2:c.19G>C, XM_011520109.1:c.19G>C, XM_017017741.2:c.19G>C, XM_017017741.1:c.19G>C, NM_001351824.2:c.19G>C, NM_001351824.1:c.19G>C, NM_001351815.2:c.19G>C, NM_001351815.1:c.19G>C, NM_001351810.2:c.19G>C, NM_001351810.1:c.19G>C, NM_001351817.2:c.19G>C, NM_001351817.1:c.19G>C, XM_047426956.1:c.19G>C, NM_001351804.1:c.19G>C, XM_047426953.1:c.19G>C, XM_047426955.1:c.19G>C, XM_047426952.1:c.19G>C, XM_047426954.1:c.19G>C, XM_047426957.1:c.148G>C, XM_047426958.1:c.148G>C, NP_001169.3:p.Asp7His, XP_011518407.2:p.Asp50His, XP_011518409.2:p.Asp50His, XP_016873227.1:p.Asp50His, XP_016873228.1:p.Asp50His, NP_001025443.1:p.Asp7His, NP_001338743.1:p.Asp7His, NP_001284648.1:p.Asp7His, NP_001338736.1:p.Asp7His, NP_001338748.1:p.Asp7His, NP_001284651.1:p.Asp7His, NP_001338734.1:p.Asp7His, NP_001338735.1:p.Asp7His, XP_011518411.1:p.Asp7His, XP_016873230.1:p.Asp7His, NP_001338753.1:p.Asp7His, NP_001338744.1:p.Asp7His, NP_001338739.1:p.Asp7His, NP_001338746.1:p.Asp7His, XP_047282912.1:p.Asp7His, NP_001338733.1:p.Asp7His, XP_047282909.1:p.Asp7His, XP_047282911.1:p.Asp7His, XP_047282908.1:p.Asp7His, XP_047282910.1:p.Asp7His, XP_047282913.1:p.Asp50His, XP_047282914.1:p.Asp50His

                                  17.

                                  rs1451645760 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>G [Show Flanks]
                                    Chromosome:
                                    11:13376705 (GRCh38)
                                    11:13398252 (GRCh37)
                                    Canonical SPDI:
                                    NC_000011.10:13376704:A:G
                                    Gene:
                                    ARNTL (Varview)
                                    Functional Consequence:
                                    non_coding_transcript_variant,genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0./0 (ALFA)
                                    G=0.000004/1 (GnomAD_exomes)
                                    G=0.000004/1 (TOPMED)
                                    G=0.000007/1 (GnomAD)
                                    HGVS:
                                    NC_000011.10:g.13376705A>G, NC_000011.9:g.13398252A>G, NM_001178.6:c.1388A>G, NM_001178.5:c.1388A>G, NM_001178.4:c.1388A>G, XM_011520105.4:c.1517A>G, XM_011520105.3:c.1517A>G, XM_011520105.2:c.1517A>G, XM_011520105.1:c.1388A>G, XM_011520107.4:c.1517A>G, XM_011520107.3:c.1517A>G, XM_011520107.2:c.1517A>G, XM_011520107.1:c.1388A>G, XM_017017738.3:c.1520A>G, XM_017017738.2:c.1520A>G, XM_017017738.1:c.1520A>G, XM_017017739.3:c.1520A>G, XM_017017739.2:c.1520A>G, XM_017017739.1:c.1520A>G, NM_001030273.3:c.1259A>G, NM_001030273.2:c.1259A>G, NM_001030273.1:c.1259A>G, NM_001030272.3:c.1388A>G, NM_001030272.2:c.1388A>G, NM_001030272.1:c.1388A>G, NR_147789.2:n.1800A>G, NR_147789.1:n.1863A>G, NR_147787.2:n.1732A>G, NR_147787.1:n.1795A>G, NM_001351812.2:c.1340A>G, NM_001351812.1:c.1340A>G, NR_147790.2:n.1898A>G, NR_147790.1:n.1961A>G, NR_147791.2:n.1895A>G, NR_147791.1:n.1958A>G, NR_147788.2:n.1879A>G, NR_147788.1:n.1942A>G, NM_001351823.2:c.1262A>G, NM_001351823.1:c.1262A>G, NM_001351808.2:c.1262A>G, NM_001351808.1:c.1262A>G, NM_001351809.2:c.1340A>G, NM_001351809.1:c.1340A>G, NM_001351818.2:c.1259A>G, NM_001351818.1:c.1259A>G, NM_001351820.2:c.1262A>G, NM_001351820.1:c.1262A>G, NR_147785.2:n.1827A>G, NR_147785.1:n.1890A>G, NR_147786.2:n.1824A>G, NR_147786.1:n.1887A>G, NM_001351813.2:c.1259A>G, NM_001351813.1:c.1259A>G, NM_001351816.2:c.1262A>G, NM_001351816.1:c.1262A>G, NM_001351814.2:c.1391A>G, NM_001351814.1:c.1391A>G, NM_001297724.2:c.1262A>G, NM_001297724.1:c.1262A>G, NM_001297719.2:c.1391A>G, NM_001297719.1:c.1391A>G, NM_001351807.2:c.1391A>G, NM_001351807.1:c.1391A>G, NM_001351819.2:c.1388A>G, NM_001351819.1:c.1388A>G, NM_001351821.2:c.1262A>G, NM_001351821.1:c.1262A>G, NM_001297722.2:c.1391A>G, NM_001297722.1:c.1391A>G, NM_001351811.2:c.641A>G, NM_001351811.1:c.641A>G, NM_001351805.2:c.1352A>G, NM_001351805.1:c.1352A>G, NM_001351806.2:c.1349A>G, NM_001351806.1:c.1349A>G, NM_001351822.2:c.1262A>G, NM_001351822.1:c.1262A>G, XM_011520109.2:c.1391A>G, XM_011520109.1:c.1391A>G, XM_017017741.2:c.1388A>G, XM_017017741.1:c.1388A>G, NM_001351824.2:c.1391A>G, NM_001351824.1:c.1391A>G, NM_001351815.2:c.1388A>G, NM_001351815.1:c.1388A>G, NM_001351810.2:c.1037A>G, NM_001351810.1:c.1037A>G, NM_001351817.2:c.1037A>G, NM_001351817.1:c.1037A>G, XM_047426956.1:c.1391A>G, NM_001351804.1:c.1388A>G, XM_024448522.1:c.1340A>G, XM_047426953.1:c.1391A>G, XM_047426955.1:c.1391A>G, XM_047426952.1:c.1391A>G, XM_047426954.1:c.1391A>G, XM_047426957.1:c.1615A>G, NP_001169.3:p.Asp463Gly, XP_011518407.2:p.Asp506Gly, XP_011518409.2:p.Asp506Gly, XP_016873227.1:p.Asp507Gly, XP_016873228.1:p.Asp507Gly, NP_001025444.1:p.Asp420Gly, NP_001025443.1:p.Asp463Gly, NP_001338741.1:p.Asp447Gly, NP_001338752.1:p.Asp421Gly, NP_001338737.1:p.Asp421Gly, NP_001338738.1:p.Asp447Gly, NP_001338747.1:p.Asp420Gly, NP_001338749.1:p.Asp421Gly, NP_001338742.1:p.Asp420Gly, NP_001338745.1:p.Asp421Gly, NP_001338743.1:p.Asp464Gly, NP_001284653.1:p.Asp421Gly, NP_001284648.1:p.Asp464Gly, NP_001338736.1:p.Asp464Gly, NP_001338748.1:p.Asp463Gly, NP_001338750.1:p.Asp421Gly, NP_001284651.1:p.Asp464Gly, NP_001338740.1:p.Asp214Gly, NP_001338734.1:p.Asp451Gly, NP_001338735.1:p.Asp450Gly, NP_001338751.1:p.Asp421Gly, XP_011518411.1:p.Asp464Gly, XP_016873230.1:p.Asp463Gly, NP_001338753.1:p.Asp464Gly, NP_001338744.1:p.Asp463Gly, NP_001338739.1:p.Asp346Gly, NP_001338746.1:p.Asp346Gly, XP_047282912.1:p.Asp464Gly, NP_001338733.1:p.Asp463Gly, XP_024304290.1:p.Asp447Gly, XP_047282909.1:p.Asp464Gly, XP_047282911.1:p.Asp464Gly, XP_047282908.1:p.Asp464Gly, XP_047282910.1:p.Asp464Gly, XP_047282913.1:p.Thr539Ala

                                    18.

                                    rs1450371323 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>G [Show Flanks]
                                      Chromosome:
                                      11:13375759 (GRCh38)
                                      11:13397306 (GRCh37)
                                      Canonical SPDI:
                                      NC_000011.10:13375758:T:G
                                      Gene:
                                      ARNTL (Varview)
                                      Functional Consequence:
                                      non_coding_transcript_variant,genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
                                      HGVS:
                                      NC_000011.10:g.13375759T>G, NC_000011.9:g.13397306T>G, NM_001178.6:c.1319T>G, NM_001178.5:c.1319T>G, NM_001178.4:c.1319T>G, XM_011520105.4:c.1448T>G, XM_011520105.3:c.1448T>G, XM_011520105.2:c.1448T>G, XM_011520105.1:c.1319T>G, XM_011520107.4:c.1448T>G, XM_011520107.3:c.1448T>G, XM_011520107.2:c.1448T>G, XM_011520107.1:c.1319T>G, XM_017017738.3:c.1451T>G, XM_017017738.2:c.1451T>G, XM_017017738.1:c.1451T>G, XM_017017739.3:c.1451T>G, XM_017017739.2:c.1451T>G, XM_017017739.1:c.1451T>G, NM_001030273.3:c.1190T>G, NM_001030273.2:c.1190T>G, NM_001030273.1:c.1190T>G, NM_001030272.3:c.1319T>G, NM_001030272.2:c.1319T>G, NM_001030272.1:c.1319T>G, NR_147789.2:n.1731T>G, NR_147789.1:n.1794T>G, NR_147787.2:n.1663T>G, NR_147787.1:n.1726T>G, NM_001351812.2:c.1271T>G, NM_001351812.1:c.1271T>G, NR_147790.2:n.1734T>G, NR_147790.1:n.1797T>G, NR_147791.2:n.1731T>G, NR_147791.1:n.1794T>G, NR_147788.2:n.1715T>G, NR_147788.1:n.1778T>G, NM_001351823.2:c.1193T>G, NM_001351823.1:c.1193T>G, NM_001351808.2:c.1193T>G, NM_001351808.1:c.1193T>G, NM_001351809.2:c.1271T>G, NM_001351809.1:c.1271T>G, NM_001351818.2:c.1190T>G, NM_001351818.1:c.1190T>G, NM_001351820.2:c.1193T>G, NM_001351820.1:c.1193T>G, NR_147785.2:n.1663T>G, NR_147785.1:n.1726T>G, NR_147786.2:n.1660T>G, NR_147786.1:n.1723T>G, NM_001351813.2:c.1190T>G, NM_001351813.1:c.1190T>G, NM_001351816.2:c.1193T>G, NM_001351816.1:c.1193T>G, NM_001351814.2:c.1322T>G, NM_001351814.1:c.1322T>G, NM_001297724.2:c.1193T>G, NM_001297724.1:c.1193T>G, NM_001297719.2:c.1322T>G, NM_001297719.1:c.1322T>G, NM_001351807.2:c.1322T>G, NM_001351807.1:c.1322T>G, NM_001351819.2:c.1319T>G, NM_001351819.1:c.1319T>G, NM_001351821.2:c.1193T>G, NM_001351821.1:c.1193T>G, NM_001297722.2:c.1322T>G, NM_001297722.1:c.1322T>G, NM_001351811.2:c.572T>G, NM_001351811.1:c.572T>G, NM_001351805.2:c.1283T>G, NM_001351805.1:c.1283T>G, NM_001351806.2:c.1280T>G, NM_001351806.1:c.1280T>G, NM_001351822.2:c.1193T>G, NM_001351822.1:c.1193T>G, XM_011520109.2:c.1322T>G, XM_011520109.1:c.1322T>G, XM_017017741.2:c.1319T>G, XM_017017741.1:c.1319T>G, NM_001351824.2:c.1322T>G, NM_001351824.1:c.1322T>G, NM_001351815.2:c.1319T>G, NM_001351815.1:c.1319T>G, NM_001351810.2:c.968T>G, NM_001351810.1:c.968T>G, NM_001351817.2:c.968T>G, NM_001351817.1:c.968T>G, XM_047426956.1:c.1322T>G, NM_001351804.1:c.1319T>G, XM_024448522.1:c.1271T>G, XM_047426953.1:c.1322T>G, XM_047426955.1:c.1322T>G, XM_047426952.1:c.1322T>G, XM_047426954.1:c.1322T>G, XM_047426957.1:c.1451T>G, NP_001169.3:p.Val440Gly, XP_011518407.2:p.Val483Gly, XP_011518409.2:p.Val483Gly, XP_016873227.1:p.Val484Gly, XP_016873228.1:p.Val484Gly, NP_001025444.1:p.Val397Gly, NP_001025443.1:p.Val440Gly, NP_001338741.1:p.Val424Gly, NP_001338752.1:p.Val398Gly, NP_001338737.1:p.Val398Gly, NP_001338738.1:p.Val424Gly, NP_001338747.1:p.Val397Gly, NP_001338749.1:p.Val398Gly, NP_001338742.1:p.Val397Gly, NP_001338745.1:p.Val398Gly, NP_001338743.1:p.Val441Gly, NP_001284653.1:p.Val398Gly, NP_001284648.1:p.Val441Gly, NP_001338736.1:p.Val441Gly, NP_001338748.1:p.Val440Gly, NP_001338750.1:p.Val398Gly, NP_001284651.1:p.Val441Gly, NP_001338740.1:p.Val191Gly, NP_001338734.1:p.Val428Gly, NP_001338735.1:p.Val427Gly, NP_001338751.1:p.Val398Gly, XP_011518411.1:p.Val441Gly, XP_016873230.1:p.Val440Gly, NP_001338753.1:p.Val441Gly, NP_001338744.1:p.Val440Gly, NP_001338739.1:p.Val323Gly, NP_001338746.1:p.Val323Gly, XP_047282912.1:p.Val441Gly, NP_001338733.1:p.Val440Gly, XP_024304290.1:p.Val424Gly, XP_047282909.1:p.Val441Gly, XP_047282911.1:p.Val441Gly, XP_047282908.1:p.Val441Gly, XP_047282910.1:p.Val441Gly, XP_047282913.1:p.Val484Gly

                                      19.

                                      rs1448895137 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>A [Show Flanks]
                                        Chromosome:
                                        11:13366671 (GRCh38)
                                        11:13388218 (GRCh37)
                                        Canonical SPDI:
                                        NC_000011.10:13366670:C:A
                                        Gene:
                                        ARNTL (Varview)
                                        Functional Consequence:
                                        5_prime_UTR_variant,non_coding_transcript_variant,coding_sequence_variant,missense_variant
                                        Validated:
                                        by frequency
                                        MAF:
                                        A=0.000004/1 (GnomAD_exomes)
                                        HGVS:
                                        NC_000011.10:g.13366671C>A, NC_000011.9:g.13388218C>A, NM_001178.6:c.559C>A, NM_001178.5:c.559C>A, NM_001178.4:c.559C>A, XM_011520105.4:c.688C>A, XM_011520105.3:c.688C>A, XM_011520105.2:c.688C>A, XM_011520105.1:c.559C>A, XM_011520107.4:c.688C>A, XM_011520107.3:c.688C>A, XM_011520107.2:c.688C>A, XM_011520107.1:c.559C>A, XM_017017738.3:c.688C>A, XM_017017738.2:c.688C>A, XM_017017738.1:c.688C>A, XM_017017739.3:c.688C>A, XM_017017739.2:c.688C>A, XM_017017739.1:c.688C>A, NM_001030273.3:c.430C>A, NM_001030273.2:c.430C>A, NM_001030273.1:c.430C>A, NM_001030272.3:c.559C>A, NM_001030272.2:c.559C>A, NM_001030272.1:c.559C>A, NR_147789.2:n.971C>A, NR_147789.1:n.1034C>A, NR_147787.2:n.900C>A, NR_147787.1:n.963C>A, NM_001351812.2:c.508C>A, NM_001351812.1:c.508C>A, NR_147790.2:n.971C>A, NR_147790.1:n.1034C>A, NR_147791.2:n.971C>A, NR_147791.1:n.1034C>A, NR_147788.2:n.955C>A, NR_147788.1:n.1018C>A, NM_001351823.2:c.430C>A, NM_001351823.1:c.430C>A, NM_001351808.2:c.430C>A, NM_001351808.1:c.430C>A, NM_001351809.2:c.508C>A, NM_001351809.1:c.508C>A, NM_001351818.2:c.430C>A, NM_001351818.1:c.430C>A, NM_001351820.2:c.430C>A, NM_001351820.1:c.430C>A, NR_147785.2:n.900C>A, NR_147785.1:n.963C>A, NR_147786.2:n.900C>A, NR_147786.1:n.963C>A, NM_001351813.2:c.430C>A, NM_001351813.1:c.430C>A, NM_001351816.2:c.430C>A, NM_001351816.1:c.430C>A, NM_001351814.2:c.559C>A, NM_001351814.1:c.559C>A, NM_001297724.2:c.430C>A, NM_001297724.1:c.430C>A, NM_001297719.2:c.559C>A, NM_001297719.1:c.559C>A, NM_001351807.2:c.559C>A, NM_001351807.1:c.559C>A, NM_001351819.2:c.559C>A, NM_001351819.1:c.559C>A, NM_001351821.2:c.430C>A, NM_001351821.1:c.430C>A, NM_001297722.2:c.559C>A, NM_001297722.1:c.559C>A, NM_001351811.2:c.-113C>A, NM_001351811.1:c.-113C>A, NM_001351805.2:c.520C>A, NM_001351805.1:c.520C>A, NM_001351806.2:c.520C>A, NM_001351806.1:c.520C>A, NM_001351822.2:c.430C>A, NM_001351822.1:c.430C>A, XM_011520109.2:c.559C>A, XM_011520109.1:c.559C>A, XM_017017741.2:c.559C>A, XM_017017741.1:c.559C>A, NM_001351824.2:c.559C>A, NM_001351824.1:c.559C>A, NM_001351815.2:c.559C>A, NM_001351815.1:c.559C>A, NM_001351810.2:c.559C>A, NM_001351810.1:c.559C>A, NM_001351817.2:c.559C>A, NM_001351817.1:c.559C>A, XM_047426956.1:c.559C>A, NM_001351804.1:c.559C>A, XM_024448522.1:c.508C>A, XM_047426953.1:c.559C>A, XM_047426955.1:c.559C>A, XM_047426952.1:c.559C>A, XM_047426954.1:c.559C>A, XM_047426957.1:c.688C>A, XM_047426958.1:c.688C>A, NP_001169.3:p.Leu187Met, XP_011518407.2:p.Leu230Met, XP_011518409.2:p.Leu230Met, XP_016873227.1:p.Leu230Met, XP_016873228.1:p.Leu230Met, NP_001025444.1:p.Leu144Met, NP_001025443.1:p.Leu187Met, NP_001338741.1:p.Leu170Met, NP_001338752.1:p.Leu144Met, NP_001338737.1:p.Leu144Met, NP_001338738.1:p.Leu170Met, NP_001338747.1:p.Leu144Met, NP_001338749.1:p.Leu144Met, NP_001338742.1:p.Leu144Met, NP_001338745.1:p.Leu144Met, NP_001338743.1:p.Leu187Met, NP_001284653.1:p.Leu144Met, NP_001284648.1:p.Leu187Met, NP_001338736.1:p.Leu187Met, NP_001338748.1:p.Leu187Met, NP_001338750.1:p.Leu144Met, NP_001284651.1:p.Leu187Met, NP_001338734.1:p.Leu174Met, NP_001338735.1:p.Leu174Met, NP_001338751.1:p.Leu144Met, XP_011518411.1:p.Leu187Met, XP_016873230.1:p.Leu187Met, NP_001338753.1:p.Leu187Met, NP_001338744.1:p.Leu187Met, NP_001338739.1:p.Leu187Met, NP_001338746.1:p.Leu187Met, XP_047282912.1:p.Leu187Met, NP_001338733.1:p.Leu187Met, XP_024304290.1:p.Leu170Met, XP_047282909.1:p.Leu187Met, XP_047282911.1:p.Leu187Met, XP_047282908.1:p.Leu187Met, XP_047282910.1:p.Leu187Met, XP_047282913.1:p.Leu230Met, XP_047282914.1:p.Leu230Met

                                        20.

                                        rs1446461583 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>G [Show Flanks]
                                          Chromosome:
                                          11:13375616 (GRCh38)
                                          11:13397163 (GRCh37)
                                          Canonical SPDI:
                                          NC_000011.10:13375615:A:G
                                          Gene:
                                          ARNTL (Varview)
                                          Functional Consequence:
                                          synonymous_variant,non_coding_transcript_variant,genic_downstream_transcript_variant,coding_sequence_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          G=0./0 (ALFA)
                                          HGVS:
                                          NC_000011.10:g.13375616A>G, NC_000011.9:g.13397163A>G, NM_001178.6:c.1176A>G, NM_001178.5:c.1176A>G, NM_001178.4:c.1176A>G, XM_011520105.4:c.1305A>G, XM_011520105.3:c.1305A>G, XM_011520105.2:c.1305A>G, XM_011520105.1:c.1176A>G, XM_011520107.4:c.1305A>G, XM_011520107.3:c.1305A>G, XM_011520107.2:c.1305A>G, XM_011520107.1:c.1176A>G, XM_017017738.3:c.1308A>G, XM_017017738.2:c.1308A>G, XM_017017738.1:c.1308A>G, XM_017017739.3:c.1308A>G, XM_017017739.2:c.1308A>G, XM_017017739.1:c.1308A>G, NM_001030273.3:c.1047A>G, NM_001030273.2:c.1047A>G, NM_001030273.1:c.1047A>G, NM_001030272.3:c.1176A>G, NM_001030272.2:c.1176A>G, NM_001030272.1:c.1176A>G, NR_147789.2:n.1588A>G, NR_147789.1:n.1651A>G, NR_147787.2:n.1520A>G, NR_147787.1:n.1583A>G, NM_001351812.2:c.1128A>G, NM_001351812.1:c.1128A>G, NR_147790.2:n.1591A>G, NR_147790.1:n.1654A>G, NR_147791.2:n.1588A>G, NR_147791.1:n.1651A>G, NR_147788.2:n.1572A>G, NR_147788.1:n.1635A>G, NM_001351823.2:c.1050A>G, NM_001351823.1:c.1050A>G, NM_001351808.2:c.1050A>G, NM_001351808.1:c.1050A>G, NM_001351809.2:c.1128A>G, NM_001351809.1:c.1128A>G, NM_001351818.2:c.1047A>G, NM_001351818.1:c.1047A>G, NM_001351820.2:c.1050A>G, NM_001351820.1:c.1050A>G, NR_147785.2:n.1520A>G, NR_147785.1:n.1583A>G, NR_147786.2:n.1517A>G, NR_147786.1:n.1580A>G, NM_001351813.2:c.1047A>G, NM_001351813.1:c.1047A>G, NM_001351816.2:c.1050A>G, NM_001351816.1:c.1050A>G, NM_001351814.2:c.1179A>G, NM_001351814.1:c.1179A>G, NM_001297724.2:c.1050A>G, NM_001297724.1:c.1050A>G, NM_001297719.2:c.1179A>G, NM_001297719.1:c.1179A>G, NM_001351807.2:c.1179A>G, NM_001351807.1:c.1179A>G, NM_001351819.2:c.1176A>G, NM_001351819.1:c.1176A>G, NM_001351821.2:c.1050A>G, NM_001351821.1:c.1050A>G, NM_001297722.2:c.1179A>G, NM_001297722.1:c.1179A>G, NM_001351811.2:c.429A>G, NM_001351811.1:c.429A>G, NM_001351805.2:c.1140A>G, NM_001351805.1:c.1140A>G, NM_001351806.2:c.1137A>G, NM_001351806.1:c.1137A>G, NM_001351822.2:c.1050A>G, NM_001351822.1:c.1050A>G, XM_011520109.2:c.1179A>G, XM_011520109.1:c.1179A>G, XM_017017741.2:c.1176A>G, XM_017017741.1:c.1176A>G, NM_001351824.2:c.1179A>G, NM_001351824.1:c.1179A>G, NM_001351815.2:c.1176A>G, NM_001351815.1:c.1176A>G, NM_001351810.2:c.825A>G, NM_001351810.1:c.825A>G, NM_001351817.2:c.825A>G, NM_001351817.1:c.825A>G, XM_047426956.1:c.1179A>G, NM_001351804.1:c.1176A>G, XM_024448522.1:c.1128A>G, XM_047426953.1:c.1179A>G, XM_047426955.1:c.1179A>G, XM_047426952.1:c.1179A>G, XM_047426954.1:c.1179A>G, XM_047426957.1:c.1308A>G

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Filters: Manage Filters

                                          Find related data

                                          Recent activity

                                          Clear Turn Off Turn On

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...