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Items: 1 to 20 of 622

1.

rs1490944179 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    15:77614116 (GRCh38)
    15:77906458 (GRCh37)
    Canonical SPDI:
    NC_000015.10:77614115:A:G
    Gene:
    LINGO1 (Varview), LOC105370906 (Varview)
    Functional Consequence:
    genic_downstream_transcript_variant,intron_variant,coding_sequence_variant,synonymous_variant
    Validated:
    by frequency
    MAF:
    G=0.000004/1 (GnomAD_exomes)
    HGVS:
    NC_000015.10:g.77614116A>G, NC_000015.9:g.77906458A>G, NM_032808.7:c.1791T>C, NM_032808.6:c.1791T>C, NM_032808.5:c.1791T>C, XM_011522118.3:c.1773T>C, XM_011522118.2:c.1773T>C, XM_011522118.1:c.1773T>C, XM_017022682.2:c.1773T>C, XM_017022682.1:c.1773T>C, NM_001301191.2:c.1773T>C, NM_001301191.1:c.1773T>C, NM_001301189.2:c.1773T>C, NM_001301189.1:c.1773T>C, NM_001301192.2:c.1773T>C, NM_001301192.1:c.1773T>C, NM_001301187.2:c.1773T>C, NM_001301187.1:c.1773T>C, XM_024450091.2:c.1773T>C, XM_024450091.1:c.1773T>C, NM_001301186.2:c.1773T>C, NM_001301186.1:c.1773T>C, NM_001301200.2:c.1773T>C, NM_001301200.1:c.1773T>C, NM_001301195.2:c.1773T>C, NM_001301195.1:c.1773T>C, NM_001301197.2:c.1773T>C, NM_001301197.1:c.1773T>C, NM_001301194.2:c.1773T>C, NM_001301194.1:c.1773T>C, NM_001301199.2:c.1773T>C, NM_001301199.1:c.1773T>C, NM_001301198.2:c.1773T>C, NM_001301198.1:c.1773T>C

    2.

    rs1489941017 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A [Show Flanks]
      Chromosome:
      15:77614490 (GRCh38)
      15:77906832 (GRCh37)
      Canonical SPDI:
      NC_000015.10:77614489:G:A
      Gene:
      LINGO1 (Varview), LOC105370906 (Varview)
      Functional Consequence:
      genic_downstream_transcript_variant,missense_variant,intron_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa
      MAF:
      A=0./0 (ALFA)
      A=0.000004/1 (GnomAD_exomes)
      HGVS:
      NC_000015.10:g.77614490G>A, NC_000015.9:g.77906832G>A, NM_032808.7:c.1417C>T, NM_032808.6:c.1417C>T, NM_032808.5:c.1417C>T, XM_011522118.3:c.1399C>T, XM_011522118.2:c.1399C>T, XM_011522118.1:c.1399C>T, XM_017022682.2:c.1399C>T, XM_017022682.1:c.1399C>T, NM_001301191.2:c.1399C>T, NM_001301191.1:c.1399C>T, NM_001301189.2:c.1399C>T, NM_001301189.1:c.1399C>T, NM_001301192.2:c.1399C>T, NM_001301192.1:c.1399C>T, NM_001301187.2:c.1399C>T, NM_001301187.1:c.1399C>T, XM_024450091.2:c.1399C>T, XM_024450091.1:c.1399C>T, NM_001301186.2:c.1399C>T, NM_001301186.1:c.1399C>T, NM_001301200.2:c.1399C>T, NM_001301200.1:c.1399C>T, NM_001301195.2:c.1399C>T, NM_001301195.1:c.1399C>T, NM_001301197.2:c.1399C>T, NM_001301197.1:c.1399C>T, NM_001301194.2:c.1399C>T, NM_001301194.1:c.1399C>T, NM_001301199.2:c.1399C>T, NM_001301199.1:c.1399C>T, NM_001301198.2:c.1399C>T, NM_001301198.1:c.1399C>T, NP_116197.4:p.Arg473Trp, XP_011520420.1:p.Arg467Trp, XP_016878171.1:p.Arg467Trp, NP_001288120.1:p.Arg467Trp, NP_001288118.1:p.Arg467Trp, NP_001288121.1:p.Arg467Trp, NP_001288116.1:p.Arg467Trp, XP_024305859.1:p.Arg467Trp, NP_001288115.1:p.Arg467Trp, NP_001288129.1:p.Arg467Trp, NP_001288124.1:p.Arg467Trp, NP_001288126.1:p.Arg467Trp, NP_001288123.1:p.Arg467Trp, NP_001288128.1:p.Arg467Trp, NP_001288127.1:p.Arg467Trp

      3.

      rs1487995400 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A [Show Flanks]
        Chromosome:
        15:77615710 (GRCh38)
        15:77908052 (GRCh37)
        Canonical SPDI:
        NC_000015.10:77615709:G:A
        Gene:
        LINGO1 (Varview), LOC105370906 (Varview)
        Functional Consequence:
        genic_downstream_transcript_variant,missense_variant,intron_variant,coding_sequence_variant
        HGVS:
        NC_000015.10:g.77615710G>A, NC_000015.9:g.77908052G>A, NM_032808.7:c.197C>T, NM_032808.6:c.197C>T, NM_032808.5:c.197C>T, XM_011522118.3:c.179C>T, XM_011522118.2:c.179C>T, XM_011522118.1:c.179C>T, XM_017022682.2:c.179C>T, XM_017022682.1:c.179C>T, NM_001301191.2:c.179C>T, NM_001301191.1:c.179C>T, NM_001301189.2:c.179C>T, NM_001301189.1:c.179C>T, NM_001301192.2:c.179C>T, NM_001301192.1:c.179C>T, NM_001301187.2:c.179C>T, NM_001301187.1:c.179C>T, XM_024450091.2:c.179C>T, XM_024450091.1:c.179C>T, NM_001301186.2:c.179C>T, NM_001301186.1:c.179C>T, NM_001301200.2:c.179C>T, NM_001301200.1:c.179C>T, NM_001301195.2:c.179C>T, NM_001301195.1:c.179C>T, NM_001301197.2:c.179C>T, NM_001301197.1:c.179C>T, NM_001301194.2:c.179C>T, NM_001301194.1:c.179C>T, NM_001301199.2:c.179C>T, NM_001301199.1:c.179C>T, NM_001301198.2:c.179C>T, NM_001301198.1:c.179C>T, NP_116197.4:p.Pro66Leu, XP_011520420.1:p.Pro60Leu, XP_016878171.1:p.Pro60Leu, NP_001288120.1:p.Pro60Leu, NP_001288118.1:p.Pro60Leu, NP_001288121.1:p.Pro60Leu, NP_001288116.1:p.Pro60Leu, XP_024305859.1:p.Pro60Leu, NP_001288115.1:p.Pro60Leu, NP_001288129.1:p.Pro60Leu, NP_001288124.1:p.Pro60Leu, NP_001288126.1:p.Pro60Leu, NP_001288123.1:p.Pro60Leu, NP_001288128.1:p.Pro60Leu, NP_001288127.1:p.Pro60Leu

        4.

        rs1485168104 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A,T [Show Flanks]
          Chromosome:
          15:77615855 (GRCh38)
          15:77908197 (GRCh37)
          Canonical SPDI:
          NC_000015.10:77615854:G:A,NC_000015.10:77615854:G:T
          Gene:
          LINGO1 (Varview), LOC105370906 (Varview)
          Functional Consequence:
          genic_downstream_transcript_variant,missense_variant,intron_variant,coding_sequence_variant
          HGVS:
          NC_000015.10:g.77615855G>A, NC_000015.10:g.77615855G>T, NC_000015.9:g.77908197G>A, NC_000015.9:g.77908197G>T, NM_032808.7:c.52C>T, NM_032808.7:c.52C>A, NM_032808.6:c.52C>T, NM_032808.6:c.52C>A, NM_032808.5:c.52C>T, NM_032808.5:c.52C>A, XM_011522118.3:c.34C>T, XM_011522118.3:c.34C>A, XM_011522118.2:c.34C>T, XM_011522118.2:c.34C>A, XM_011522118.1:c.34C>T, XM_011522118.1:c.34C>A, XM_017022682.2:c.34C>T, XM_017022682.2:c.34C>A, XM_017022682.1:c.34C>T, XM_017022682.1:c.34C>A, NM_001301191.2:c.34C>T, NM_001301191.2:c.34C>A, NM_001301191.1:c.34C>T, NM_001301191.1:c.34C>A, NM_001301189.2:c.34C>T, NM_001301189.2:c.34C>A, NM_001301189.1:c.34C>T, NM_001301189.1:c.34C>A, NM_001301192.2:c.34C>T, NM_001301192.2:c.34C>A, NM_001301192.1:c.34C>T, NM_001301192.1:c.34C>A, NM_001301187.2:c.34C>T, NM_001301187.2:c.34C>A, NM_001301187.1:c.34C>T, NM_001301187.1:c.34C>A, XM_024450091.2:c.34C>T, XM_024450091.2:c.34C>A, XM_024450091.1:c.34C>T, XM_024450091.1:c.34C>A, NM_001301186.2:c.34C>T, NM_001301186.2:c.34C>A, NM_001301186.1:c.34C>T, NM_001301186.1:c.34C>A, NM_001301200.2:c.34C>T, NM_001301200.2:c.34C>A, NM_001301200.1:c.34C>T, NM_001301200.1:c.34C>A, NM_001301195.2:c.34C>T, NM_001301195.2:c.34C>A, NM_001301195.1:c.34C>T, NM_001301195.1:c.34C>A, NM_001301197.2:c.34C>T, NM_001301197.2:c.34C>A, NM_001301197.1:c.34C>T, NM_001301197.1:c.34C>A, NM_001301194.2:c.34C>T, NM_001301194.2:c.34C>A, NM_001301194.1:c.34C>T, NM_001301194.1:c.34C>A, NM_001301199.2:c.34C>T, NM_001301199.2:c.34C>A, NM_001301199.1:c.34C>T, NM_001301199.1:c.34C>A, NM_001301198.2:c.34C>T, NM_001301198.2:c.34C>A, NM_001301198.1:c.34C>T, NM_001301198.1:c.34C>A, NP_116197.4:p.Pro18Ser, NP_116197.4:p.Pro18Thr, XP_011520420.1:p.Pro12Ser, XP_011520420.1:p.Pro12Thr, XP_016878171.1:p.Pro12Ser, XP_016878171.1:p.Pro12Thr, NP_001288120.1:p.Pro12Ser, NP_001288120.1:p.Pro12Thr, NP_001288118.1:p.Pro12Ser, NP_001288118.1:p.Pro12Thr, NP_001288121.1:p.Pro12Ser, NP_001288121.1:p.Pro12Thr, NP_001288116.1:p.Pro12Ser, NP_001288116.1:p.Pro12Thr, XP_024305859.1:p.Pro12Ser, XP_024305859.1:p.Pro12Thr, NP_001288115.1:p.Pro12Ser, NP_001288115.1:p.Pro12Thr, NP_001288129.1:p.Pro12Ser, NP_001288129.1:p.Pro12Thr, NP_001288124.1:p.Pro12Ser, NP_001288124.1:p.Pro12Thr, NP_001288126.1:p.Pro12Ser, NP_001288126.1:p.Pro12Thr, NP_001288123.1:p.Pro12Ser, NP_001288123.1:p.Pro12Thr, NP_001288128.1:p.Pro12Ser, NP_001288128.1:p.Pro12Thr, NP_001288127.1:p.Pro12Ser, NP_001288127.1:p.Pro12Thr

          5.

          rs1481140231 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>A [Show Flanks]
            Chromosome:
            15:77614675 (GRCh38)
            15:77907017 (GRCh37)
            Canonical SPDI:
            NC_000015.10:77614674:G:A
            Gene:
            LINGO1 (Varview), LOC105370906 (Varview)
            Functional Consequence:
            missense_variant,intron_variant,coding_sequence_variant,genic_downstream_transcript_variant
            HGVS:
            NC_000015.10:g.77614675G>A, NC_000015.9:g.77907017G>A, NM_032808.7:c.1232C>T, NM_032808.6:c.1232C>T, NM_032808.5:c.1232C>T, XM_011522118.3:c.1214C>T, XM_011522118.2:c.1214C>T, XM_011522118.1:c.1214C>T, XM_017022682.2:c.1214C>T, XM_017022682.1:c.1214C>T, NM_001301191.2:c.1214C>T, NM_001301191.1:c.1214C>T, NM_001301189.2:c.1214C>T, NM_001301189.1:c.1214C>T, NM_001301192.2:c.1214C>T, NM_001301192.1:c.1214C>T, NM_001301187.2:c.1214C>T, NM_001301187.1:c.1214C>T, XM_024450091.2:c.1214C>T, XM_024450091.1:c.1214C>T, NM_001301186.2:c.1214C>T, NM_001301186.1:c.1214C>T, NM_001301200.2:c.1214C>T, NM_001301200.1:c.1214C>T, NM_001301195.2:c.1214C>T, NM_001301195.1:c.1214C>T, NM_001301197.2:c.1214C>T, NM_001301197.1:c.1214C>T, NM_001301194.2:c.1214C>T, NM_001301194.1:c.1214C>T, NM_001301199.2:c.1214C>T, NM_001301199.1:c.1214C>T, NM_001301198.2:c.1214C>T, NM_001301198.1:c.1214C>T, NP_116197.4:p.Pro411Leu, XP_011520420.1:p.Pro405Leu, XP_016878171.1:p.Pro405Leu, NP_001288120.1:p.Pro405Leu, NP_001288118.1:p.Pro405Leu, NP_001288121.1:p.Pro405Leu, NP_001288116.1:p.Pro405Leu, XP_024305859.1:p.Pro405Leu, NP_001288115.1:p.Pro405Leu, NP_001288129.1:p.Pro405Leu, NP_001288124.1:p.Pro405Leu, NP_001288126.1:p.Pro405Leu, NP_001288123.1:p.Pro405Leu, NP_001288128.1:p.Pro405Leu, NP_001288127.1:p.Pro405Leu

            6.

            rs1480681202 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              15:77614759 (GRCh38)
              15:77907101 (GRCh37)
              Canonical SPDI:
              NC_000015.10:77614758:C:T
              Gene:
              LINGO1 (Varview), LOC105370906 (Varview)
              Functional Consequence:
              missense_variant,intron_variant,coding_sequence_variant,genic_downstream_transcript_variant
              HGVS:
              NC_000015.10:g.77614759C>T, NC_000015.9:g.77907101C>T, NM_032808.7:c.1148G>A, NM_032808.6:c.1148G>A, NM_032808.5:c.1148G>A, XM_011522118.3:c.1130G>A, XM_011522118.2:c.1130G>A, XM_011522118.1:c.1130G>A, XM_017022682.2:c.1130G>A, XM_017022682.1:c.1130G>A, NM_001301191.2:c.1130G>A, NM_001301191.1:c.1130G>A, NM_001301189.2:c.1130G>A, NM_001301189.1:c.1130G>A, NM_001301192.2:c.1130G>A, NM_001301192.1:c.1130G>A, NM_001301187.2:c.1130G>A, NM_001301187.1:c.1130G>A, XM_024450091.2:c.1130G>A, XM_024450091.1:c.1130G>A, NM_001301186.2:c.1130G>A, NM_001301186.1:c.1130G>A, NM_001301200.2:c.1130G>A, NM_001301200.1:c.1130G>A, NM_001301195.2:c.1130G>A, NM_001301195.1:c.1130G>A, NM_001301197.2:c.1130G>A, NM_001301197.1:c.1130G>A, NM_001301194.2:c.1130G>A, NM_001301194.1:c.1130G>A, NM_001301199.2:c.1130G>A, NM_001301199.1:c.1130G>A, NM_001301198.2:c.1130G>A, NM_001301198.1:c.1130G>A, NP_116197.4:p.Arg383His, XP_011520420.1:p.Arg377His, XP_016878171.1:p.Arg377His, NP_001288120.1:p.Arg377His, NP_001288118.1:p.Arg377His, NP_001288121.1:p.Arg377His, NP_001288116.1:p.Arg377His, XP_024305859.1:p.Arg377His, NP_001288115.1:p.Arg377His, NP_001288129.1:p.Arg377His, NP_001288124.1:p.Arg377His, NP_001288126.1:p.Arg377His, NP_001288123.1:p.Arg377His, NP_001288128.1:p.Arg377His, NP_001288127.1:p.Arg377His

              7.

              rs1480029782 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>T [Show Flanks]
                Chromosome:
                15:77614270 (GRCh38)
                15:77906612 (GRCh37)
                Canonical SPDI:
                NC_000015.10:77614269:G:T
                Gene:
                LINGO1 (Varview), LOC105370906 (Varview)
                Functional Consequence:
                missense_variant,intron_variant,coding_sequence_variant,genic_downstream_transcript_variant
                Validated:
                by frequency
                MAF:
                T=0.000004/1 (GnomAD_exomes)
                HGVS:
                NC_000015.10:g.77614270G>T, NC_000015.9:g.77906612G>T, NM_032808.7:c.1637C>A, NM_032808.6:c.1637C>A, NM_032808.5:c.1637C>A, XM_011522118.3:c.1619C>A, XM_011522118.2:c.1619C>A, XM_011522118.1:c.1619C>A, XM_017022682.2:c.1619C>A, XM_017022682.1:c.1619C>A, NM_001301191.2:c.1619C>A, NM_001301191.1:c.1619C>A, NM_001301189.2:c.1619C>A, NM_001301189.1:c.1619C>A, NM_001301192.2:c.1619C>A, NM_001301192.1:c.1619C>A, NM_001301187.2:c.1619C>A, NM_001301187.1:c.1619C>A, XM_024450091.2:c.1619C>A, XM_024450091.1:c.1619C>A, NM_001301186.2:c.1619C>A, NM_001301186.1:c.1619C>A, NM_001301200.2:c.1619C>A, NM_001301200.1:c.1619C>A, NM_001301195.2:c.1619C>A, NM_001301195.1:c.1619C>A, NM_001301197.2:c.1619C>A, NM_001301197.1:c.1619C>A, NM_001301194.2:c.1619C>A, NM_001301194.1:c.1619C>A, NM_001301199.2:c.1619C>A, NM_001301199.1:c.1619C>A, NM_001301198.2:c.1619C>A, NM_001301198.1:c.1619C>A, NP_116197.4:p.Ala546Asp, XP_011520420.1:p.Ala540Asp, XP_016878171.1:p.Ala540Asp, NP_001288120.1:p.Ala540Asp, NP_001288118.1:p.Ala540Asp, NP_001288121.1:p.Ala540Asp, NP_001288116.1:p.Ala540Asp, XP_024305859.1:p.Ala540Asp, NP_001288115.1:p.Ala540Asp, NP_001288129.1:p.Ala540Asp, NP_001288124.1:p.Ala540Asp, NP_001288126.1:p.Ala540Asp, NP_001288123.1:p.Ala540Asp, NP_001288128.1:p.Ala540Asp, NP_001288127.1:p.Ala540Asp

                8.

                rs1479507037 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>A,C [Show Flanks]
                  Chromosome:
                  15:77614413 (GRCh38)
                  15:77906755 (GRCh37)
                  Canonical SPDI:
                  NC_000015.10:77614412:G:A,NC_000015.10:77614412:G:C
                  Gene:
                  LINGO1 (Varview), LOC105370906 (Varview)
                  Functional Consequence:
                  intron_variant,missense_variant,genic_downstream_transcript_variant,synonymous_variant,coding_sequence_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  C=0./0 (ALFA)
                  A=0.000004/1 (GnomAD_exomes)
                  A=0.000004/1 (TOPMED)
                  HGVS:
                  NC_000015.10:g.77614413G>A, NC_000015.10:g.77614413G>C, NC_000015.9:g.77906755G>A, NC_000015.9:g.77906755G>C, NM_032808.7:c.1494C>T, NM_032808.7:c.1494C>G, NM_032808.6:c.1494C>T, NM_032808.6:c.1494C>G, NM_032808.5:c.1494C>T, NM_032808.5:c.1494C>G, XM_011522118.3:c.1476C>T, XM_011522118.3:c.1476C>G, XM_011522118.2:c.1476C>T, XM_011522118.2:c.1476C>G, XM_011522118.1:c.1476C>T, XM_011522118.1:c.1476C>G, XM_017022682.2:c.1476C>T, XM_017022682.2:c.1476C>G, XM_017022682.1:c.1476C>T, XM_017022682.1:c.1476C>G, NM_001301191.2:c.1476C>T, NM_001301191.2:c.1476C>G, NM_001301191.1:c.1476C>T, NM_001301191.1:c.1476C>G, NM_001301189.2:c.1476C>T, NM_001301189.2:c.1476C>G, NM_001301189.1:c.1476C>T, NM_001301189.1:c.1476C>G, NM_001301192.2:c.1476C>T, NM_001301192.2:c.1476C>G, NM_001301192.1:c.1476C>T, NM_001301192.1:c.1476C>G, NM_001301187.2:c.1476C>T, NM_001301187.2:c.1476C>G, NM_001301187.1:c.1476C>T, NM_001301187.1:c.1476C>G, XM_024450091.2:c.1476C>T, XM_024450091.2:c.1476C>G, XM_024450091.1:c.1476C>T, XM_024450091.1:c.1476C>G, NM_001301186.2:c.1476C>T, NM_001301186.2:c.1476C>G, NM_001301186.1:c.1476C>T, NM_001301186.1:c.1476C>G, NM_001301200.2:c.1476C>T, NM_001301200.2:c.1476C>G, NM_001301200.1:c.1476C>T, NM_001301200.1:c.1476C>G, NM_001301195.2:c.1476C>T, NM_001301195.2:c.1476C>G, NM_001301195.1:c.1476C>T, NM_001301195.1:c.1476C>G, NM_001301197.2:c.1476C>T, NM_001301197.2:c.1476C>G, NM_001301197.1:c.1476C>T, NM_001301197.1:c.1476C>G, NM_001301194.2:c.1476C>T, NM_001301194.2:c.1476C>G, NM_001301194.1:c.1476C>T, NM_001301194.1:c.1476C>G, NM_001301199.2:c.1476C>T, NM_001301199.2:c.1476C>G, NM_001301199.1:c.1476C>T, NM_001301199.1:c.1476C>G, NM_001301198.2:c.1476C>T, NM_001301198.2:c.1476C>G, NM_001301198.1:c.1476C>T, NM_001301198.1:c.1476C>G, NP_116197.4:p.Ile498Met, XP_011520420.1:p.Ile492Met, XP_016878171.1:p.Ile492Met, NP_001288120.1:p.Ile492Met, NP_001288118.1:p.Ile492Met, NP_001288121.1:p.Ile492Met, NP_001288116.1:p.Ile492Met, XP_024305859.1:p.Ile492Met, NP_001288115.1:p.Ile492Met, NP_001288129.1:p.Ile492Met, NP_001288124.1:p.Ile492Met, NP_001288126.1:p.Ile492Met, NP_001288123.1:p.Ile492Met, NP_001288128.1:p.Ile492Met, NP_001288127.1:p.Ile492Met

                  9.

                  rs1477354909 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A [Show Flanks]
                    Chromosome:
                    15:77615716 (GRCh38)
                    15:77908058 (GRCh37)
                    Canonical SPDI:
                    NC_000015.10:77615715:G:A
                    Gene:
                    LINGO1 (Varview), LOC105370906 (Varview)
                    Functional Consequence:
                    missense_variant,intron_variant,coding_sequence_variant,genic_downstream_transcript_variant
                    HGVS:
                    NC_000015.10:g.77615716G>A, NC_000015.9:g.77908058G>A, NM_032808.7:c.191C>T, NM_032808.6:c.191C>T, NM_032808.5:c.191C>T, XM_011522118.3:c.173C>T, XM_011522118.2:c.173C>T, XM_011522118.1:c.173C>T, XM_017022682.2:c.173C>T, XM_017022682.1:c.173C>T, NM_001301191.2:c.173C>T, NM_001301191.1:c.173C>T, NM_001301189.2:c.173C>T, NM_001301189.1:c.173C>T, NM_001301192.2:c.173C>T, NM_001301192.1:c.173C>T, NM_001301187.2:c.173C>T, NM_001301187.1:c.173C>T, XM_024450091.2:c.173C>T, XM_024450091.1:c.173C>T, NM_001301186.2:c.173C>T, NM_001301186.1:c.173C>T, NM_001301200.2:c.173C>T, NM_001301200.1:c.173C>T, NM_001301195.2:c.173C>T, NM_001301195.1:c.173C>T, NM_001301197.2:c.173C>T, NM_001301197.1:c.173C>T, NM_001301194.2:c.173C>T, NM_001301194.1:c.173C>T, NM_001301199.2:c.173C>T, NM_001301199.1:c.173C>T, NM_001301198.2:c.173C>T, NM_001301198.1:c.173C>T, NP_116197.4:p.Ala64Val, XP_011520420.1:p.Ala58Val, XP_016878171.1:p.Ala58Val, NP_001288120.1:p.Ala58Val, NP_001288118.1:p.Ala58Val, NP_001288121.1:p.Ala58Val, NP_001288116.1:p.Ala58Val, XP_024305859.1:p.Ala58Val, NP_001288115.1:p.Ala58Val, NP_001288129.1:p.Ala58Val, NP_001288124.1:p.Ala58Val, NP_001288126.1:p.Ala58Val, NP_001288123.1:p.Ala58Val, NP_001288128.1:p.Ala58Val, NP_001288127.1:p.Ala58Val

                    10.

                    rs1476762168 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A [Show Flanks]
                      Chromosome:
                      15:77615859 (GRCh38)
                      15:77908201 (GRCh37)
                      Canonical SPDI:
                      NC_000015.10:77615858:G:A
                      Gene:
                      LINGO1 (Varview), LOC105370906 (Varview)
                      Functional Consequence:
                      intron_variant,coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0./0 (ALFA)
                      A=0.000004/1 (TOPMED)
                      A=0.000007/1 (GnomAD)
                      HGVS:
                      NC_000015.10:g.77615859G>A, NC_000015.9:g.77908201G>A, NM_032808.7:c.48C>T, NM_032808.6:c.48C>T, NM_032808.5:c.48C>T, XM_011522118.3:c.30C>T, XM_011522118.2:c.30C>T, XM_011522118.1:c.30C>T, XM_017022682.2:c.30C>T, XM_017022682.1:c.30C>T, NM_001301191.2:c.30C>T, NM_001301191.1:c.30C>T, NM_001301189.2:c.30C>T, NM_001301189.1:c.30C>T, NM_001301192.2:c.30C>T, NM_001301192.1:c.30C>T, NM_001301187.2:c.30C>T, NM_001301187.1:c.30C>T, XM_024450091.2:c.30C>T, XM_024450091.1:c.30C>T, NM_001301186.2:c.30C>T, NM_001301186.1:c.30C>T, NM_001301200.2:c.30C>T, NM_001301200.1:c.30C>T, NM_001301195.2:c.30C>T, NM_001301195.1:c.30C>T, NM_001301197.2:c.30C>T, NM_001301197.1:c.30C>T, NM_001301194.2:c.30C>T, NM_001301194.1:c.30C>T, NM_001301199.2:c.30C>T, NM_001301199.1:c.30C>T, NM_001301198.2:c.30C>T, NM_001301198.1:c.30C>T

                      11.

                      rs1472174518 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>A [Show Flanks]
                        Chromosome:
                        15:77615814 (GRCh38)
                        15:77908156 (GRCh37)
                        Canonical SPDI:
                        NC_000015.10:77615813:C:A
                        Gene:
                        LINGO1 (Varview), LOC105370906 (Varview)
                        Functional Consequence:
                        intron_variant,coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
                        HGVS:
                        NC_000015.10:g.77615814C>A, NC_000015.9:g.77908156C>A, NM_032808.7:c.93G>T, NM_032808.6:c.93G>T, NM_032808.5:c.93G>T, XM_011522118.3:c.75G>T, XM_011522118.2:c.75G>T, XM_011522118.1:c.75G>T, XM_017022682.2:c.75G>T, XM_017022682.1:c.75G>T, NM_001301191.2:c.75G>T, NM_001301191.1:c.75G>T, NM_001301189.2:c.75G>T, NM_001301189.1:c.75G>T, NM_001301192.2:c.75G>T, NM_001301192.1:c.75G>T, NM_001301187.2:c.75G>T, NM_001301187.1:c.75G>T, XM_024450091.2:c.75G>T, XM_024450091.1:c.75G>T, NM_001301186.2:c.75G>T, NM_001301186.1:c.75G>T, NM_001301200.2:c.75G>T, NM_001301200.1:c.75G>T, NM_001301195.2:c.75G>T, NM_001301195.1:c.75G>T, NM_001301197.2:c.75G>T, NM_001301197.1:c.75G>T, NM_001301194.2:c.75G>T, NM_001301194.1:c.75G>T, NM_001301199.2:c.75G>T, NM_001301199.1:c.75G>T, NM_001301198.2:c.75G>T, NM_001301198.1:c.75G>T

                        12.

                        rs1471414411 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A [Show Flanks]
                          Chromosome:
                          15:77614497 (GRCh38)
                          15:77906839 (GRCh37)
                          Canonical SPDI:
                          NC_000015.10:77614496:G:A
                          Gene:
                          LINGO1 (Varview), LOC105370906 (Varview)
                          Functional Consequence:
                          intron_variant,coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0./0 (ALFA)
                          A=0.000004/1 (TOPMED)
                          A=0.000007/1 (GnomAD)
                          HGVS:
                          NC_000015.10:g.77614497G>A, NC_000015.9:g.77906839G>A, NM_032808.7:c.1410C>T, NM_032808.6:c.1410C>T, NM_032808.5:c.1410C>T, XM_011522118.3:c.1392C>T, XM_011522118.2:c.1392C>T, XM_011522118.1:c.1392C>T, XM_017022682.2:c.1392C>T, XM_017022682.1:c.1392C>T, NM_001301191.2:c.1392C>T, NM_001301191.1:c.1392C>T, NM_001301189.2:c.1392C>T, NM_001301189.1:c.1392C>T, NM_001301192.2:c.1392C>T, NM_001301192.1:c.1392C>T, NM_001301187.2:c.1392C>T, NM_001301187.1:c.1392C>T, XM_024450091.2:c.1392C>T, XM_024450091.1:c.1392C>T, NM_001301186.2:c.1392C>T, NM_001301186.1:c.1392C>T, NM_001301200.2:c.1392C>T, NM_001301200.1:c.1392C>T, NM_001301195.2:c.1392C>T, NM_001301195.1:c.1392C>T, NM_001301197.2:c.1392C>T, NM_001301197.1:c.1392C>T, NM_001301194.2:c.1392C>T, NM_001301194.1:c.1392C>T, NM_001301199.2:c.1392C>T, NM_001301199.1:c.1392C>T, NM_001301198.2:c.1392C>T, NM_001301198.1:c.1392C>T

                          13.

                          rs1470892677 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A [Show Flanks]
                            Chromosome:
                            15:77614632 (GRCh38)
                            15:77906974 (GRCh37)
                            Canonical SPDI:
                            NC_000015.10:77614631:G:A
                            Gene:
                            LINGO1 (Varview), LOC105370906 (Varview)
                            Functional Consequence:
                            intron_variant,coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
                            HGVS:
                            NC_000015.10:g.77614632G>A, NC_000015.9:g.77906974G>A, NM_032808.7:c.1275C>T, NM_032808.6:c.1275C>T, NM_032808.5:c.1275C>T, XM_011522118.3:c.1257C>T, XM_011522118.2:c.1257C>T, XM_011522118.1:c.1257C>T, XM_017022682.2:c.1257C>T, XM_017022682.1:c.1257C>T, NM_001301191.2:c.1257C>T, NM_001301191.1:c.1257C>T, NM_001301189.2:c.1257C>T, NM_001301189.1:c.1257C>T, NM_001301192.2:c.1257C>T, NM_001301192.1:c.1257C>T, NM_001301187.2:c.1257C>T, NM_001301187.1:c.1257C>T, XM_024450091.2:c.1257C>T, XM_024450091.1:c.1257C>T, NM_001301186.2:c.1257C>T, NM_001301186.1:c.1257C>T, NM_001301200.2:c.1257C>T, NM_001301200.1:c.1257C>T, NM_001301195.2:c.1257C>T, NM_001301195.1:c.1257C>T, NM_001301197.2:c.1257C>T, NM_001301197.1:c.1257C>T, NM_001301194.2:c.1257C>T, NM_001301194.1:c.1257C>T, NM_001301199.2:c.1257C>T, NM_001301199.1:c.1257C>T, NM_001301198.2:c.1257C>T, NM_001301198.1:c.1257C>T

                            14.

                            rs1465499742 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>C [Show Flanks]
                              Chromosome:
                              15:77614826 (GRCh38)
                              15:77907168 (GRCh37)
                              Canonical SPDI:
                              NC_000015.10:77614825:G:C
                              Gene:
                              LINGO1 (Varview), LOC105370906 (Varview)
                              Functional Consequence:
                              missense_variant,intron_variant,coding_sequence_variant,genic_downstream_transcript_variant
                              Validated:
                              by frequency
                              MAF:
                              C=0.000004/1 (GnomAD_exomes)
                              HGVS:
                              NC_000015.10:g.77614826G>C, NC_000015.9:g.77907168G>C, NM_032808.7:c.1081C>G, NM_032808.6:c.1081C>G, NM_032808.5:c.1081C>G, XM_011522118.3:c.1063C>G, XM_011522118.2:c.1063C>G, XM_011522118.1:c.1063C>G, XM_017022682.2:c.1063C>G, XM_017022682.1:c.1063C>G, NM_001301191.2:c.1063C>G, NM_001301191.1:c.1063C>G, NM_001301189.2:c.1063C>G, NM_001301189.1:c.1063C>G, NM_001301192.2:c.1063C>G, NM_001301192.1:c.1063C>G, NM_001301187.2:c.1063C>G, NM_001301187.1:c.1063C>G, XM_024450091.2:c.1063C>G, XM_024450091.1:c.1063C>G, NM_001301186.2:c.1063C>G, NM_001301186.1:c.1063C>G, NM_001301200.2:c.1063C>G, NM_001301200.1:c.1063C>G, NM_001301195.2:c.1063C>G, NM_001301195.1:c.1063C>G, NM_001301197.2:c.1063C>G, NM_001301197.1:c.1063C>G, NM_001301194.2:c.1063C>G, NM_001301194.1:c.1063C>G, NM_001301199.2:c.1063C>G, NM_001301199.1:c.1063C>G, NM_001301198.2:c.1063C>G, NM_001301198.1:c.1063C>G, NP_116197.4:p.Leu361Val, XP_011520420.1:p.Leu355Val, XP_016878171.1:p.Leu355Val, NP_001288120.1:p.Leu355Val, NP_001288118.1:p.Leu355Val, NP_001288121.1:p.Leu355Val, NP_001288116.1:p.Leu355Val, XP_024305859.1:p.Leu355Val, NP_001288115.1:p.Leu355Val, NP_001288129.1:p.Leu355Val, NP_001288124.1:p.Leu355Val, NP_001288126.1:p.Leu355Val, NP_001288123.1:p.Leu355Val, NP_001288128.1:p.Leu355Val, NP_001288127.1:p.Leu355Val

                              15.

                              rs1465261241 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>T [Show Flanks]
                                Chromosome:
                                15:77615324 (GRCh38)
                                15:77907666 (GRCh37)
                                Canonical SPDI:
                                NC_000015.10:77615323:G:T
                                Gene:
                                LINGO1 (Varview), LOC105370906 (Varview)
                                Functional Consequence:
                                missense_variant,intron_variant,coding_sequence_variant,genic_downstream_transcript_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000004/1 (TOPMED)
                                T=0.000014/2 (GnomAD)
                                HGVS:
                                NC_000015.10:g.77615324G>T, NC_000015.9:g.77907666G>T, NM_032808.7:c.583C>A, NM_032808.6:c.583C>A, NM_032808.5:c.583C>A, XM_011522118.3:c.565C>A, XM_011522118.2:c.565C>A, XM_011522118.1:c.565C>A, XM_017022682.2:c.565C>A, XM_017022682.1:c.565C>A, NM_001301191.2:c.565C>A, NM_001301191.1:c.565C>A, NM_001301189.2:c.565C>A, NM_001301189.1:c.565C>A, NM_001301192.2:c.565C>A, NM_001301192.1:c.565C>A, NM_001301187.2:c.565C>A, NM_001301187.1:c.565C>A, XM_024450091.2:c.565C>A, XM_024450091.1:c.565C>A, NM_001301186.2:c.565C>A, NM_001301186.1:c.565C>A, NM_001301200.2:c.565C>A, NM_001301200.1:c.565C>A, NM_001301195.2:c.565C>A, NM_001301195.1:c.565C>A, NM_001301197.2:c.565C>A, NM_001301197.1:c.565C>A, NM_001301194.2:c.565C>A, NM_001301194.1:c.565C>A, NM_001301199.2:c.565C>A, NM_001301199.1:c.565C>A, NM_001301198.2:c.565C>A, NM_001301198.1:c.565C>A, NP_116197.4:p.Gln195Lys, XP_011520420.1:p.Gln189Lys, XP_016878171.1:p.Gln189Lys, NP_001288120.1:p.Gln189Lys, NP_001288118.1:p.Gln189Lys, NP_001288121.1:p.Gln189Lys, NP_001288116.1:p.Gln189Lys, XP_024305859.1:p.Gln189Lys, NP_001288115.1:p.Gln189Lys, NP_001288129.1:p.Gln189Lys, NP_001288124.1:p.Gln189Lys, NP_001288126.1:p.Gln189Lys, NP_001288123.1:p.Gln189Lys, NP_001288128.1:p.Gln189Lys, NP_001288127.1:p.Gln189Lys

                                16.

                                rs1464019915 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>T [Show Flanks]
                                  Chromosome:
                                  15:77615820 (GRCh38)
                                  15:77908162 (GRCh37)
                                  Canonical SPDI:
                                  NC_000015.10:77615819:C:T
                                  Gene:
                                  LINGO1 (Varview), LOC105370906 (Varview)
                                  Functional Consequence:
                                  intron_variant,coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
                                  Validated:
                                  by frequency
                                  MAF:
                                  T=0.000007/1 (GnomAD_exomes)
                                  HGVS:
                                  NC_000015.10:g.77615820C>T, NC_000015.9:g.77908162C>T, NM_032808.7:c.87G>A, NM_032808.6:c.87G>A, NM_032808.5:c.87G>A, XM_011522118.3:c.69G>A, XM_011522118.2:c.69G>A, XM_011522118.1:c.69G>A, XM_017022682.2:c.69G>A, XM_017022682.1:c.69G>A, NM_001301191.2:c.69G>A, NM_001301191.1:c.69G>A, NM_001301189.2:c.69G>A, NM_001301189.1:c.69G>A, NM_001301192.2:c.69G>A, NM_001301192.1:c.69G>A, NM_001301187.2:c.69G>A, NM_001301187.1:c.69G>A, XM_024450091.2:c.69G>A, XM_024450091.1:c.69G>A, NM_001301186.2:c.69G>A, NM_001301186.1:c.69G>A, NM_001301200.2:c.69G>A, NM_001301200.1:c.69G>A, NM_001301195.2:c.69G>A, NM_001301195.1:c.69G>A, NM_001301197.2:c.69G>A, NM_001301197.1:c.69G>A, NM_001301194.2:c.69G>A, NM_001301194.1:c.69G>A, NM_001301199.2:c.69G>A, NM_001301199.1:c.69G>A, NM_001301198.2:c.69G>A, NM_001301198.1:c.69G>A

                                  17.

                                  rs1462553656 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>T [Show Flanks]
                                    Chromosome:
                                    15:77614787 (GRCh38)
                                    15:77907129 (GRCh37)
                                    Canonical SPDI:
                                    NC_000015.10:77614786:C:T
                                    Gene:
                                    LINGO1 (Varview), LOC105370906 (Varview)
                                    Functional Consequence:
                                    missense_variant,intron_variant,coding_sequence_variant,genic_downstream_transcript_variant
                                    HGVS:
                                    NC_000015.10:g.77614787C>T, NC_000015.9:g.77907129C>T, NM_032808.7:c.1120G>A, NM_032808.6:c.1120G>A, NM_032808.5:c.1120G>A, XM_011522118.3:c.1102G>A, XM_011522118.2:c.1102G>A, XM_011522118.1:c.1102G>A, XM_017022682.2:c.1102G>A, XM_017022682.1:c.1102G>A, NM_001301191.2:c.1102G>A, NM_001301191.1:c.1102G>A, NM_001301189.2:c.1102G>A, NM_001301189.1:c.1102G>A, NM_001301192.2:c.1102G>A, NM_001301192.1:c.1102G>A, NM_001301187.2:c.1102G>A, NM_001301187.1:c.1102G>A, XM_024450091.2:c.1102G>A, XM_024450091.1:c.1102G>A, NM_001301186.2:c.1102G>A, NM_001301186.1:c.1102G>A, NM_001301200.2:c.1102G>A, NM_001301200.1:c.1102G>A, NM_001301195.2:c.1102G>A, NM_001301195.1:c.1102G>A, NM_001301197.2:c.1102G>A, NM_001301197.1:c.1102G>A, NM_001301194.2:c.1102G>A, NM_001301194.1:c.1102G>A, NM_001301199.2:c.1102G>A, NM_001301199.1:c.1102G>A, NM_001301198.2:c.1102G>A, NM_001301198.1:c.1102G>A, NP_116197.4:p.Asp374Asn, XP_011520420.1:p.Asp368Asn, XP_016878171.1:p.Asp368Asn, NP_001288120.1:p.Asp368Asn, NP_001288118.1:p.Asp368Asn, NP_001288121.1:p.Asp368Asn, NP_001288116.1:p.Asp368Asn, XP_024305859.1:p.Asp368Asn, NP_001288115.1:p.Asp368Asn, NP_001288129.1:p.Asp368Asn, NP_001288124.1:p.Asp368Asn, NP_001288126.1:p.Asp368Asn, NP_001288123.1:p.Asp368Asn, NP_001288128.1:p.Asp368Asn, NP_001288127.1:p.Asp368Asn

                                    18.

                                    rs1462118103 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>A [Show Flanks]
                                      Chromosome:
                                      15:77614614 (GRCh38)
                                      15:77906956 (GRCh37)
                                      Canonical SPDI:
                                      NC_000015.10:77614613:G:A
                                      Gene:
                                      LINGO1 (Varview), LOC105370906 (Varview)
                                      Functional Consequence:
                                      intron_variant,coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
                                      HGVS:
                                      NC_000015.10:g.77614614G>A, NC_000015.9:g.77906956G>A, NM_032808.7:c.1293C>T, NM_032808.6:c.1293C>T, NM_032808.5:c.1293C>T, XM_011522118.3:c.1275C>T, XM_011522118.2:c.1275C>T, XM_011522118.1:c.1275C>T, XM_017022682.2:c.1275C>T, XM_017022682.1:c.1275C>T, NM_001301191.2:c.1275C>T, NM_001301191.1:c.1275C>T, NM_001301189.2:c.1275C>T, NM_001301189.1:c.1275C>T, NM_001301192.2:c.1275C>T, NM_001301192.1:c.1275C>T, NM_001301187.2:c.1275C>T, NM_001301187.1:c.1275C>T, XM_024450091.2:c.1275C>T, XM_024450091.1:c.1275C>T, NM_001301186.2:c.1275C>T, NM_001301186.1:c.1275C>T, NM_001301200.2:c.1275C>T, NM_001301200.1:c.1275C>T, NM_001301195.2:c.1275C>T, NM_001301195.1:c.1275C>T, NM_001301197.2:c.1275C>T, NM_001301197.1:c.1275C>T, NM_001301194.2:c.1275C>T, NM_001301194.1:c.1275C>T, NM_001301199.2:c.1275C>T, NM_001301199.1:c.1275C>T, NM_001301198.2:c.1275C>T, NM_001301198.1:c.1275C>T

                                      19.

                                      rs1457117177 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>A [Show Flanks]
                                        Chromosome:
                                        15:77615217 (GRCh38)
                                        15:77907559 (GRCh37)
                                        Canonical SPDI:
                                        NC_000015.10:77615216:G:A
                                        Gene:
                                        LINGO1 (Varview), LOC105370906 (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,synonymous_variant,intron_variant,genic_downstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        A=0./0 (ALFA)
                                        HGVS:
                                        NC_000015.10:g.77615217G>A, NC_000015.9:g.77907559G>A, NM_032808.7:c.690C>T, NM_032808.6:c.690C>T, NM_032808.5:c.690C>T, XM_011522118.3:c.672C>T, XM_011522118.2:c.672C>T, XM_011522118.1:c.672C>T, XM_017022682.2:c.672C>T, XM_017022682.1:c.672C>T, NM_001301191.2:c.672C>T, NM_001301191.1:c.672C>T, NM_001301189.2:c.672C>T, NM_001301189.1:c.672C>T, NM_001301192.2:c.672C>T, NM_001301192.1:c.672C>T, NM_001301187.2:c.672C>T, NM_001301187.1:c.672C>T, XM_024450091.2:c.672C>T, XM_024450091.1:c.672C>T, NM_001301186.2:c.672C>T, NM_001301186.1:c.672C>T, NM_001301200.2:c.672C>T, NM_001301200.1:c.672C>T, NM_001301195.2:c.672C>T, NM_001301195.1:c.672C>T, NM_001301197.2:c.672C>T, NM_001301197.1:c.672C>T, NM_001301194.2:c.672C>T, NM_001301194.1:c.672C>T, NM_001301199.2:c.672C>T, NM_001301199.1:c.672C>T, NM_001301198.2:c.672C>T, NM_001301198.1:c.672C>T

                                        20.

                                        rs1454114601 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          15:77615304 (GRCh38)
                                          15:77907646 (GRCh37)
                                          Canonical SPDI:
                                          NC_000015.10:77615303:G:A
                                          Gene:
                                          LINGO1 (Varview), LOC105370906 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,synonymous_variant,intron_variant,genic_downstream_transcript_variant
                                          HGVS:
                                          NC_000015.10:g.77615304G>A, NC_000015.9:g.77907646G>A, NM_032808.7:c.603C>T, NM_032808.6:c.603C>T, NM_032808.5:c.603C>T, XM_011522118.3:c.585C>T, XM_011522118.2:c.585C>T, XM_011522118.1:c.585C>T, XM_017022682.2:c.585C>T, XM_017022682.1:c.585C>T, NM_001301191.2:c.585C>T, NM_001301191.1:c.585C>T, NM_001301189.2:c.585C>T, NM_001301189.1:c.585C>T, NM_001301192.2:c.585C>T, NM_001301192.1:c.585C>T, NM_001301187.2:c.585C>T, NM_001301187.1:c.585C>T, XM_024450091.2:c.585C>T, XM_024450091.1:c.585C>T, NM_001301186.2:c.585C>T, NM_001301186.1:c.585C>T, NM_001301200.2:c.585C>T, NM_001301200.1:c.585C>T, NM_001301195.2:c.585C>T, NM_001301195.1:c.585C>T, NM_001301197.2:c.585C>T, NM_001301197.1:c.585C>T, NM_001301194.2:c.585C>T, NM_001301194.1:c.585C>T, NM_001301199.2:c.585C>T, NM_001301199.1:c.585C>T, NM_001301198.2:c.585C>T, NM_001301198.1:c.585C>T

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