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Items: 1 to 20 of 456

1.

rs1487796765 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>A [Show Flanks]
    Chromosome:
    1:231626885 (GRCh38)
    1:231762631 (GRCh37)
    Canonical SPDI:
    NC_000001.11:231626884:T:A
    Gene:
    DISC1 (Varview), TSNAX-DISC1 (Varview)
    Functional Consequence:
    intron_variant,synonymous_variant,coding_sequence_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0./0 (ALFA)
    A=0.000008/2 (TOPMED)
    A=0.000022/2 (GnomAD_exomes)
    HGVS:
    NC_000001.11:g.231626885T>A, NC_000001.10:g.231762631T>A, NG_011681.2:g.5071T>A, NM_018662.3:c.18T>A, NM_018662.2:c.18T>A, NM_001164537.2:c.18T>A, NM_001164537.1:c.18T>A, NM_001012957.2:c.18T>A, NM_001012957.1:c.18T>A, NM_001164540.2:c.18T>A, NM_001164540.1:c.18T>A, NM_001164538.2:c.18T>A, NM_001164538.1:c.18T>A, NM_001164541.2:c.18T>A, NM_001164541.1:c.18T>A, NM_001164550.2:c.18T>A, NM_001164550.1:c.18T>A, NM_001164552.2:c.18T>A, NM_001164552.1:c.18T>A, NM_001164544.2:c.18T>A, NM_001164544.1:c.18T>A, NM_001164542.2:c.18T>A, NM_001164542.1:c.18T>A, NM_001164553.2:c.18T>A, NM_001164553.1:c.18T>A, NM_001164539.2:c.18T>A, NM_001164539.1:c.18T>A, NM_001012958.2:c.18T>A, NM_001012958.1:c.18T>A, NM_001164545.2:c.18T>A, NM_001164545.1:c.18T>A, NM_001164547.2:c.18T>A, NM_001164547.1:c.18T>A, NM_001164548.2:c.18T>A, NM_001164548.1:c.18T>A, NM_001164546.2:c.18T>A, NM_001164546.1:c.18T>A, NM_001164549.2:c.18T>A, NM_001164549.1:c.18T>A, NM_001012959.2:c.18T>A, NM_001012959.1:c.18T>A, NM_001164551.2:c.18T>A, NM_001164551.1:c.18T>A, NM_001164554.2:c.18T>A, NM_001164554.1:c.18T>A, NM_001164555.2:c.18T>A, NM_001164555.1:c.18T>A, NM_001164556.2:c.18T>A, NM_001164556.1:c.18T>A
    2.

    rs1486438784 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A [Show Flanks]
      Chromosome:
      1:231694725 (GRCh38)
      1:231830471 (GRCh37)
      Canonical SPDI:
      NC_000001.11:231694724:G:A
      Gene:
      DISC1 (Varview), TSNAX-DISC1 (Varview)
      Functional Consequence:
      non_coding_transcript_variant,intron_variant,missense_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      A=0.000071/1 (ALFA)
      A=0.000004/1 (GnomAD_exomes)
      A=0.000008/2 (TOPMED)
      A=0.000014/2 (GnomAD)
      HGVS:
      NC_000001.11:g.231694725G>A, NC_000001.10:g.231830471G>A, NG_011681.2:g.72911G>A, NM_018662.3:c.967G>A, NM_018662.2:c.967G>A, NM_001164537.2:c.967G>A, NM_001164537.1:c.967G>A, NM_001012957.2:c.967G>A, NM_001012957.1:c.967G>A, NM_001164540.2:c.967G>A, NM_001164540.1:c.967G>A, NM_001164538.2:c.967G>A, NM_001164538.1:c.967G>A, NM_001164541.2:c.967G>A, NM_001164541.1:c.967G>A, NM_001164550.2:c.967G>A, NM_001164550.1:c.967G>A, NM_001164552.2:c.967G>A, NM_001164552.1:c.967G>A, NM_001164544.2:c.967G>A, NM_001164544.1:c.967G>A, NM_001164542.2:c.967G>A, NM_001164542.1:c.967G>A, NM_001164553.2:c.967G>A, NM_001164553.1:c.967G>A, NM_001164539.2:c.967G>A, NM_001164539.1:c.967G>A, NM_001012958.2:c.967G>A, NM_001012958.1:c.967G>A, NM_001164545.2:c.967G>A, NM_001164545.1:c.967G>A, NM_001164547.2:c.967G>A, NM_001164547.1:c.967G>A, NM_001164548.2:c.967G>A, NM_001164548.1:c.967G>A, NM_001164546.2:c.967G>A, NM_001164546.1:c.967G>A, NM_001164549.2:c.967G>A, NM_001164549.1:c.967G>A, NM_001012959.2:c.967G>A, NM_001012959.1:c.967G>A, NM_001164551.2:c.967G>A, NM_001164551.1:c.967G>A, NM_001164554.2:c.967G>A, NM_001164554.1:c.967G>A, NM_001164555.2:c.967G>A, NM_001164555.1:c.967G>A, NR_028393.1:n.1688G>A, NR_028394.1:n.1816G>A, NR_028395.1:n.1816G>A, NR_028396.1:n.1688G>A, NR_028397.1:n.1553G>A, NR_028398.1:n.1307G>A, NR_028399.1:n.1923G>A, NR_028400.1:n.1795G>A, NP_061132.2:p.Ala323Thr, NP_001158009.1:p.Ala323Thr, NP_001012975.1:p.Ala323Thr, NP_001158012.1:p.Ala323Thr, NP_001158010.1:p.Ala323Thr, NP_001158013.1:p.Ala323Thr, NP_001158022.1:p.Ala323Thr, NP_001158024.1:p.Ala323Thr, NP_001158016.1:p.Ala323Thr, NP_001158014.1:p.Ala323Thr, NP_001158025.1:p.Ala323Thr, NP_001158011.1:p.Ala323Thr, NP_001012976.1:p.Ala323Thr, NP_001158017.1:p.Ala323Thr, NP_001158019.1:p.Ala323Thr, NP_001158020.1:p.Ala323Thr, NP_001158018.1:p.Ala323Thr, NP_001158021.1:p.Ala323Thr, NP_001012977.1:p.Ala323Thr, NP_001158023.1:p.Ala323Thr, NP_001158026.1:p.Ala323Thr, NP_001158027.1:p.Ala323Thr
      3.

      rs1476384887 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>G [Show Flanks]
        Chromosome:
        1:231694749 (GRCh38)
        1:231830495 (GRCh37)
        Canonical SPDI:
        NC_000001.11:231694748:A:G
        Gene:
        DISC1 (Varview), TSNAX-DISC1 (Varview)
        Functional Consequence:
        non_coding_transcript_variant,intron_variant,coding_sequence_variant,missense_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        G=0.000031/1 (ALFA)
        G=0.000004/1 (GnomAD_exomes)
        G=0.000007/1 (GnomAD)
        G=0.000008/2 (TOPMED)
        HGVS:
        NC_000001.11:g.231694749A>G, NC_000001.10:g.231830495A>G, NG_011681.2:g.72935A>G, NM_018662.3:c.991A>G, NM_018662.2:c.991A>G, NM_001164537.2:c.991A>G, NM_001164537.1:c.991A>G, NM_001012957.2:c.991A>G, NM_001012957.1:c.991A>G, NM_001164540.2:c.991A>G, NM_001164540.1:c.991A>G, NM_001164538.2:c.991A>G, NM_001164538.1:c.991A>G, NM_001164541.2:c.991A>G, NM_001164541.1:c.991A>G, NM_001164550.2:c.991A>G, NM_001164550.1:c.991A>G, NM_001164552.2:c.991A>G, NM_001164552.1:c.991A>G, NM_001164544.2:c.991A>G, NM_001164544.1:c.991A>G, NM_001164542.2:c.991A>G, NM_001164542.1:c.991A>G, NM_001164553.2:c.991A>G, NM_001164553.1:c.991A>G, NM_001164539.2:c.991A>G, NM_001164539.1:c.991A>G, NM_001012958.2:c.991A>G, NM_001012958.1:c.991A>G, NM_001164545.2:c.991A>G, NM_001164545.1:c.991A>G, NM_001164547.2:c.991A>G, NM_001164547.1:c.991A>G, NM_001164548.2:c.991A>G, NM_001164548.1:c.991A>G, NM_001164546.2:c.991A>G, NM_001164546.1:c.991A>G, NM_001164549.2:c.991A>G, NM_001164549.1:c.991A>G, NM_001012959.2:c.991A>G, NM_001012959.1:c.991A>G, NM_001164551.2:c.991A>G, NM_001164551.1:c.991A>G, NM_001164554.2:c.991A>G, NM_001164554.1:c.991A>G, NM_001164555.2:c.991A>G, NM_001164555.1:c.991A>G, NR_028393.1:n.1712A>G, NR_028394.1:n.1840A>G, NR_028395.1:n.1840A>G, NR_028396.1:n.1712A>G, NR_028397.1:n.1577A>G, NR_028398.1:n.1331A>G, NR_028399.1:n.1947A>G, NR_028400.1:n.1819A>G, NP_061132.2:p.Arg331Gly, NP_001158009.1:p.Arg331Gly, NP_001012975.1:p.Arg331Gly, NP_001158012.1:p.Arg331Gly, NP_001158010.1:p.Arg331Gly, NP_001158013.1:p.Arg331Gly, NP_001158022.1:p.Arg331Gly, NP_001158024.1:p.Arg331Gly, NP_001158016.1:p.Arg331Gly, NP_001158014.1:p.Arg331Gly, NP_001158025.1:p.Arg331Gly, NP_001158011.1:p.Arg331Gly, NP_001012976.1:p.Arg331Gly, NP_001158017.1:p.Arg331Gly, NP_001158019.1:p.Arg331Gly, NP_001158020.1:p.Arg331Gly, NP_001158018.1:p.Arg331Gly, NP_001158021.1:p.Arg331Gly, NP_001012977.1:p.Arg331Gly, NP_001158023.1:p.Arg331Gly, NP_001158026.1:p.Arg331Gly, NP_001158027.1:p.Arg331Gly
        4.

        rs1474002143 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>T [Show Flanks]
          Chromosome:
          1:231694035 (GRCh38)
          1:231829781 (GRCh37)
          Canonical SPDI:
          NC_000001.11:231694034:C:T
          Gene:
          DISC1 (Varview), TSNAX-DISC1 (Varview)
          Functional Consequence:
          missense_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0./0 (ALFA)
          T=0.000004/1 (GnomAD_exomes)
          T=0.000004/1 (TOPMED)
          HGVS:
          NC_000001.11:g.231694035C>T, NC_000001.10:g.231829781C>T, NG_011681.2:g.72221C>T, NM_018662.3:c.277C>T, NM_018662.2:c.277C>T, NM_001164537.2:c.277C>T, NM_001164537.1:c.277C>T, NM_001012957.2:c.277C>T, NM_001012957.1:c.277C>T, NM_001164540.2:c.277C>T, NM_001164540.1:c.277C>T, NM_001164538.2:c.277C>T, NM_001164538.1:c.277C>T, NM_001164541.2:c.277C>T, NM_001164541.1:c.277C>T, NM_001164550.2:c.277C>T, NM_001164550.1:c.277C>T, NM_001164552.2:c.277C>T, NM_001164552.1:c.277C>T, NM_001164544.2:c.277C>T, NM_001164544.1:c.277C>T, NM_001164542.2:c.277C>T, NM_001164542.1:c.277C>T, NM_001164553.2:c.277C>T, NM_001164553.1:c.277C>T, NM_001164539.2:c.277C>T, NM_001164539.1:c.277C>T, NM_001012958.2:c.277C>T, NM_001012958.1:c.277C>T, NM_001164545.2:c.277C>T, NM_001164545.1:c.277C>T, NM_001164547.2:c.277C>T, NM_001164547.1:c.277C>T, NM_001164548.2:c.277C>T, NM_001164548.1:c.277C>T, NM_001164546.2:c.277C>T, NM_001164546.1:c.277C>T, NM_001164549.2:c.277C>T, NM_001164549.1:c.277C>T, NM_001012959.2:c.277C>T, NM_001012959.1:c.277C>T, NM_001164551.2:c.277C>T, NM_001164551.1:c.277C>T, NM_001164554.2:c.277C>T, NM_001164554.1:c.277C>T, NM_001164555.2:c.277C>T, NM_001164555.1:c.277C>T, NR_028393.1:n.998C>T, NR_028394.1:n.1126C>T, NR_028395.1:n.1126C>T, NR_028396.1:n.998C>T, NR_028397.1:n.863C>T, NR_028398.1:n.617C>T, NR_028399.1:n.1233C>T, NR_028400.1:n.1105C>T, NP_061132.2:p.Leu93Phe, NP_001158009.1:p.Leu93Phe, NP_001012975.1:p.Leu93Phe, NP_001158012.1:p.Leu93Phe, NP_001158010.1:p.Leu93Phe, NP_001158013.1:p.Leu93Phe, NP_001158022.1:p.Leu93Phe, NP_001158024.1:p.Leu93Phe, NP_001158016.1:p.Leu93Phe, NP_001158014.1:p.Leu93Phe, NP_001158025.1:p.Leu93Phe, NP_001158011.1:p.Leu93Phe, NP_001012976.1:p.Leu93Phe, NP_001158017.1:p.Leu93Phe, NP_001158019.1:p.Leu93Phe, NP_001158020.1:p.Leu93Phe, NP_001158018.1:p.Leu93Phe, NP_001158021.1:p.Leu93Phe, NP_001012977.1:p.Leu93Phe, NP_001158023.1:p.Leu93Phe, NP_001158026.1:p.Leu93Phe, NP_001158027.1:p.Leu93Phe
          5.

          rs1469382298 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            ->GAGGCGGCGGC [Show Flanks]
            Chromosome:
            1:231693862 (GRCh38)
            1:231829609 (GRCh37)
            Canonical SPDI:
            NC_000001.11:231693862:GAGGCGGCGGC:GAGGCGGCGGCGAGGCGGCGGC
            Gene:
            DISC1 (Varview), TSNAX-DISC1 (Varview)
            Functional Consequence:
            frameshift_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
            Validated:
            by cluster
            HGVS:
            NC_000001.11:g.231693863_231693873dup, NC_000001.10:g.231829609_231829619dup, NG_011681.2:g.72049_72059dup, NM_018662.3:c.105_115dup, NM_018662.2:c.105_115dup, NM_001164537.2:c.105_115dup, NM_001164537.1:c.105_115dup, NM_001012957.2:c.105_115dup, NM_001012957.1:c.105_115dup, NM_001164540.2:c.105_115dup, NM_001164540.1:c.105_115dup, NM_001164538.2:c.105_115dup, NM_001164538.1:c.105_115dup, NM_001164541.2:c.105_115dup, NM_001164541.1:c.105_115dup, NM_001164550.2:c.105_115dup, NM_001164550.1:c.105_115dup, NM_001164552.2:c.105_115dup, NM_001164552.1:c.105_115dup, NM_001164544.2:c.105_115dup, NM_001164544.1:c.105_115dup, NM_001164542.2:c.105_115dup, NM_001164542.1:c.105_115dup, NM_001164553.2:c.105_115dup, NM_001164553.1:c.105_115dup, NM_001164539.2:c.105_115dup, NM_001164539.1:c.105_115dup, NM_001012958.2:c.105_115dup, NM_001012958.1:c.105_115dup, NM_001164545.2:c.105_115dup, NM_001164545.1:c.105_115dup, NM_001164547.2:c.105_115dup, NM_001164547.1:c.105_115dup, NM_001164548.2:c.105_115dup, NM_001164548.1:c.105_115dup, NM_001164546.2:c.105_115dup, NM_001164546.1:c.105_115dup, NM_001164549.2:c.105_115dup, NM_001164549.1:c.105_115dup, NM_001012959.2:c.105_115dup, NM_001012959.1:c.105_115dup, NM_001164551.2:c.105_115dup, NM_001164551.1:c.105_115dup, NM_001164554.2:c.105_115dup, NM_001164554.1:c.105_115dup, NM_001164555.2:c.105_115dup, NM_001164555.1:c.105_115dup, NR_028393.1:n.826_836dup, NR_028394.1:n.954_964dup, NR_028395.1:n.954_964dup, NR_028396.1:n.826_836dup, NR_028397.1:n.691_701dup, NR_028398.1:n.445_455dup, NR_028399.1:n.1061_1071dup, NR_028400.1:n.933_943dup, NP_061132.2:p.Leu39fs, NP_001158009.1:p.Leu39fs, NP_001012975.1:p.Leu39fs, NP_001158012.1:p.Leu39fs, NP_001158010.1:p.Leu39fs, NP_001158013.1:p.Leu39fs, NP_001158022.1:p.Leu39fs, NP_001158024.1:p.Leu39fs, NP_001158016.1:p.Leu39fs, NP_001158014.1:p.Leu39fs, NP_001158025.1:p.Leu39fs, NP_001158011.1:p.Leu39fs, NP_001012976.1:p.Leu39fs, NP_001158017.1:p.Leu39fs, NP_001158019.1:p.Leu39fs, NP_001158020.1:p.Leu39fs, NP_001158018.1:p.Leu39fs, NP_001158021.1:p.Leu39fs, NP_001012977.1:p.Leu39fs, NP_001158023.1:p.Leu39fs, NP_001158026.1:p.Leu39fs, NP_001158027.1:p.Leu39fs
            6.

            rs1468456861 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              CTGGCTGTGG>- [Show Flanks]
              Chromosome:
              1:231694687 (GRCh38)
              1:231830433 (GRCh37)
              Canonical SPDI:
              NC_000001.11:231694683:TGGCTGGCTGTGG:TGG
              Gene:
              DISC1 (Varview), TSNAX-DISC1 (Varview)
              Functional Consequence:
              frameshift_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
              Validated:
              by frequency,by alfa
              MAF:
              TGG=0./0 (ALFA)
              -=0.000004/1 (TOPMED)
              HGVS:
              NC_000001.11:g.231694687_231694696del, NC_000001.10:g.231830433_231830442del, NG_011681.2:g.72873_72882del, NM_018662.3:c.929_938del, NM_018662.2:c.929_938del, NM_001164537.2:c.929_938del, NM_001164537.1:c.929_938del, NM_001012957.2:c.929_938del, NM_001012957.1:c.929_938del, NM_001164540.2:c.929_938del, NM_001164540.1:c.929_938del, NM_001164538.2:c.929_938del, NM_001164538.1:c.929_938del, NM_001164541.2:c.929_938del, NM_001164541.1:c.929_938del, NM_001164550.2:c.929_938del, NM_001164550.1:c.929_938del, NM_001164552.2:c.929_938del, NM_001164552.1:c.929_938del, NM_001164544.2:c.929_938del, NM_001164544.1:c.929_938del, NM_001164542.2:c.929_938del, NM_001164542.1:c.929_938del, NM_001164553.2:c.929_938del, NM_001164553.1:c.929_938del, NM_001164539.2:c.929_938del, NM_001164539.1:c.929_938del, NM_001012958.2:c.929_938del, NM_001012958.1:c.929_938del, NM_001164545.2:c.929_938del, NM_001164545.1:c.929_938del, NM_001164547.2:c.929_938del, NM_001164547.1:c.929_938del, NM_001164548.2:c.929_938del, NM_001164548.1:c.929_938del, NM_001164546.2:c.929_938del, NM_001164546.1:c.929_938del, NM_001164549.2:c.929_938del, NM_001164549.1:c.929_938del, NM_001012959.2:c.929_938del, NM_001012959.1:c.929_938del, NM_001164551.2:c.929_938del, NM_001164551.1:c.929_938del, NM_001164554.2:c.929_938del, NM_001164554.1:c.929_938del, NM_001164555.2:c.929_938del, NM_001164555.1:c.929_938del, NR_028393.1:n.1650_1659del, NR_028394.1:n.1778_1787del, NR_028395.1:n.1778_1787del, NR_028396.1:n.1650_1659del, NR_028397.1:n.1515_1524del, NR_028398.1:n.1269_1278del, NR_028399.1:n.1885_1894del, NR_028400.1:n.1757_1766del, NP_061132.2:p.Ala310fs, NP_001158009.1:p.Ala310fs, NP_001012975.1:p.Ala310fs, NP_001158012.1:p.Ala310fs, NP_001158010.1:p.Ala310fs, NP_001158013.1:p.Ala310fs, NP_001158022.1:p.Ala310fs, NP_001158024.1:p.Ala310fs, NP_001158016.1:p.Ala310fs, NP_001158014.1:p.Ala310fs, NP_001158025.1:p.Ala310fs, NP_001158011.1:p.Ala310fs, NP_001012976.1:p.Ala310fs, NP_001158017.1:p.Ala310fs, NP_001158019.1:p.Ala310fs, NP_001158020.1:p.Ala310fs, NP_001158018.1:p.Ala310fs, NP_001158021.1:p.Ala310fs, NP_001012977.1:p.Ala310fs, NP_001158023.1:p.Ala310fs, NP_001158026.1:p.Ala310fs, NP_001158027.1:p.Ala310fs
              7.

              rs1467388316 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>C [Show Flanks]
                Chromosome:
                1:231749956 (GRCh38)
                1:231885702 (GRCh37)
                Canonical SPDI:
                NC_000001.11:231749955:T:C
                Gene:
                DISC1 (Varview), TSNAX-DISC1 (Varview)
                Functional Consequence:
                missense_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,3_prime_UTR_variant
                Validated:
                by frequency,by alfa
                MAF:
                C=0.000031/1 (ALFA)
                C=0.000004/1 (GnomAD_exomes)
                HGVS:
                NC_000001.11:g.231749956T>C, NC_000001.10:g.231885702T>C, NG_011681.2:g.128142T>C, NM_018662.3:c.1148T>C, NM_018662.2:c.1148T>C, NM_001164537.2:c.1244T>C, NM_001164537.1:c.1244T>C, NM_001012957.2:c.1148T>C, NM_001012957.1:c.1148T>C, NM_001164540.2:c.1148T>C, NM_001164540.1:c.1148T>C, NM_001164538.2:c.1148T>C, NM_001164538.1:c.1148T>C, NM_001164541.2:c.1148T>C, NM_001164541.1:c.1148T>C, NM_001164544.2:c.1148T>C, NM_001164544.1:c.1148T>C, NM_001164542.2:c.1148T>C, NM_001164542.1:c.1148T>C, NM_001164539.2:c.1148T>C, NM_001164539.1:c.1148T>C, NM_001164545.2:c.1148T>C, NM_001164545.1:c.1148T>C, NM_001164547.2:c.1148T>C, NM_001164547.1:c.1148T>C, NM_001164548.2:c.1148T>C, NM_001164548.1:c.1148T>C, NM_001164546.2:c.1148T>C, NM_001164546.1:c.1148T>C, NM_001164549.2:c.1148T>C, NM_001164549.1:c.1148T>C, NM_001012959.2:c.1148T>C, NM_001012959.1:c.1148T>C, NM_001164551.2:c.1148T>C, NM_001164551.1:c.1148T>C, NM_001164555.2:c.*7T>C, NM_001164555.1:c.*7T>C, NM_001164556.2:c.98T>C, NM_001164556.1:c.98T>C, NR_028393.1:n.1869T>C, NR_028394.1:n.1997T>C, NR_028395.1:n.1997T>C, NR_028396.1:n.1869T>C, NR_028397.1:n.1734T>C, NR_028398.1:n.1488T>C, NR_028400.1:n.1906T>C, NP_061132.2:p.Leu383Pro, NP_001158009.1:p.Leu415Pro, NP_001012975.1:p.Leu383Pro, NP_001158012.1:p.Leu383Pro, NP_001158010.1:p.Leu383Pro, NP_001158013.1:p.Leu383Pro, NP_001158016.1:p.Leu383Pro, NP_001158014.1:p.Leu383Pro, NP_001158011.1:p.Leu383Pro, NP_001158017.1:p.Leu383Pro, NP_001158019.1:p.Leu383Pro, NP_001158020.1:p.Leu383Pro, NP_001158018.1:p.Leu383Pro, NP_001158021.1:p.Leu383Pro, NP_001012977.1:p.Leu383Pro, NP_001158023.1:p.Leu383Pro, NP_001158028.1:p.Leu33Pro
                8.

                rs1467229857 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G,T [Show Flanks]
                  Chromosome:
                  1:231694277 (GRCh38)
                  1:231830023 (GRCh37)
                  Canonical SPDI:
                  NC_000001.11:231694276:A:G,NC_000001.11:231694276:A:T
                  Gene:
                  DISC1 (Varview), TSNAX-DISC1 (Varview)
                  Functional Consequence:
                  non_coding_transcript_variant,synonymous_variant,coding_sequence_variant,intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  T=0./0 (ALFA)
                  G=0.000004/1 (GnomAD_exomes)
                  T=0.000004/1 (TOPMED)
                  HGVS:
                  NC_000001.11:g.231694277A>G, NC_000001.11:g.231694277A>T, NC_000001.10:g.231830023A>G, NC_000001.10:g.231830023A>T, NG_011681.2:g.72463A>G, NG_011681.2:g.72463A>T, NM_018662.3:c.519A>G, NM_018662.3:c.519A>T, NM_018662.2:c.519A>G, NM_018662.2:c.519A>T, NM_001164537.2:c.519A>G, NM_001164537.2:c.519A>T, NM_001164537.1:c.519A>G, NM_001164537.1:c.519A>T, NM_001012957.2:c.519A>G, NM_001012957.2:c.519A>T, NM_001012957.1:c.519A>G, NM_001012957.1:c.519A>T, NM_001164540.2:c.519A>G, NM_001164540.2:c.519A>T, NM_001164540.1:c.519A>G, NM_001164540.1:c.519A>T, NM_001164538.2:c.519A>G, NM_001164538.2:c.519A>T, NM_001164538.1:c.519A>G, NM_001164538.1:c.519A>T, NM_001164541.2:c.519A>G, NM_001164541.2:c.519A>T, NM_001164541.1:c.519A>G, NM_001164541.1:c.519A>T, NM_001164550.2:c.519A>G, NM_001164550.2:c.519A>T, NM_001164550.1:c.519A>G, NM_001164550.1:c.519A>T, NM_001164552.2:c.519A>G, NM_001164552.2:c.519A>T, NM_001164552.1:c.519A>G, NM_001164552.1:c.519A>T, NM_001164544.2:c.519A>G, NM_001164544.2:c.519A>T, NM_001164544.1:c.519A>G, NM_001164544.1:c.519A>T, NM_001164542.2:c.519A>G, NM_001164542.2:c.519A>T, NM_001164542.1:c.519A>G, NM_001164542.1:c.519A>T, NM_001164553.2:c.519A>G, NM_001164553.2:c.519A>T, NM_001164553.1:c.519A>G, NM_001164553.1:c.519A>T, NM_001164539.2:c.519A>G, NM_001164539.2:c.519A>T, NM_001164539.1:c.519A>G, NM_001164539.1:c.519A>T, NM_001012958.2:c.519A>G, NM_001012958.2:c.519A>T, NM_001012958.1:c.519A>G, NM_001012958.1:c.519A>T, NM_001164545.2:c.519A>G, NM_001164545.2:c.519A>T, NM_001164545.1:c.519A>G, NM_001164545.1:c.519A>T, NM_001164547.2:c.519A>G, NM_001164547.2:c.519A>T, NM_001164547.1:c.519A>G, NM_001164547.1:c.519A>T, NM_001164548.2:c.519A>G, NM_001164548.2:c.519A>T, NM_001164548.1:c.519A>G, NM_001164548.1:c.519A>T, NM_001164546.2:c.519A>G, NM_001164546.2:c.519A>T, NM_001164546.1:c.519A>G, NM_001164546.1:c.519A>T, NM_001164549.2:c.519A>G, NM_001164549.2:c.519A>T, NM_001164549.1:c.519A>G, NM_001164549.1:c.519A>T, NM_001012959.2:c.519A>G, NM_001012959.2:c.519A>T, NM_001012959.1:c.519A>G, NM_001012959.1:c.519A>T, NM_001164551.2:c.519A>G, NM_001164551.2:c.519A>T, NM_001164551.1:c.519A>G, NM_001164551.1:c.519A>T, NM_001164554.2:c.519A>G, NM_001164554.2:c.519A>T, NM_001164554.1:c.519A>G, NM_001164554.1:c.519A>T, NM_001164555.2:c.519A>G, NM_001164555.2:c.519A>T, NM_001164555.1:c.519A>G, NM_001164555.1:c.519A>T, NR_028393.1:n.1240A>G, NR_028393.1:n.1240A>T, NR_028394.1:n.1368A>G, NR_028394.1:n.1368A>T, NR_028395.1:n.1368A>G, NR_028395.1:n.1368A>T, NR_028396.1:n.1240A>G, NR_028396.1:n.1240A>T, NR_028397.1:n.1105A>G, NR_028397.1:n.1105A>T, NR_028398.1:n.859A>G, NR_028398.1:n.859A>T, NR_028399.1:n.1475A>G, NR_028399.1:n.1475A>T, NR_028400.1:n.1347A>G, NR_028400.1:n.1347A>T
                  9.

                  rs1464491607 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    C>A [Show Flanks]
                    Chromosome:
                    1:231750014 (GRCh38)
                    1:231885760 (GRCh37)
                    Canonical SPDI:
                    NC_000001.11:231750013:C:A
                    Gene:
                    DISC1 (Varview), TSNAX-DISC1 (Varview)
                    Functional Consequence:
                    missense_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,3_prime_UTR_variant
                    Validated:
                    by frequency
                    MAF:
                    A=0.000004/1 (GnomAD_exomes)
                    HGVS:
                    NC_000001.11:g.231750014C>A, NC_000001.10:g.231885760C>A, NG_011681.2:g.128200C>A, NM_018662.3:c.1206C>A, NM_018662.2:c.1206C>A, NM_001164537.2:c.1302C>A, NM_001164537.1:c.1302C>A, NM_001012957.2:c.1206C>A, NM_001012957.1:c.1206C>A, NM_001164540.2:c.1206C>A, NM_001164540.1:c.1206C>A, NM_001164538.2:c.1206C>A, NM_001164538.1:c.1206C>A, NM_001164541.2:c.1206C>A, NM_001164541.1:c.1206C>A, NM_001164544.2:c.1206C>A, NM_001164544.1:c.1206C>A, NM_001164542.2:c.1206C>A, NM_001164542.1:c.1206C>A, NM_001164539.2:c.1206C>A, NM_001164539.1:c.1206C>A, NM_001164545.2:c.1206C>A, NM_001164545.1:c.1206C>A, NM_001164547.2:c.1206C>A, NM_001164547.1:c.1206C>A, NM_001164548.2:c.1206C>A, NM_001164548.1:c.1206C>A, NM_001164546.2:c.1206C>A, NM_001164546.1:c.1206C>A, NM_001164549.2:c.1206C>A, NM_001164549.1:c.1206C>A, NM_001012959.2:c.1206C>A, NM_001012959.1:c.1206C>A, NM_001164551.2:c.1206C>A, NM_001164551.1:c.1206C>A, NM_001164555.2:c.*65C>A, NM_001164555.1:c.*65C>A, NM_001164556.2:c.156C>A, NM_001164556.1:c.156C>A, NR_028393.1:n.1927C>A, NR_028394.1:n.2055C>A, NR_028395.1:n.2055C>A, NR_028396.1:n.1927C>A, NR_028397.1:n.1792C>A, NR_028398.1:n.1546C>A, NR_028400.1:n.1964C>A, NP_061132.2:p.Ser402Arg, NP_001158009.1:p.Ser434Arg, NP_001012975.1:p.Ser402Arg, NP_001158012.1:p.Ser402Arg, NP_001158010.1:p.Ser402Arg, NP_001158013.1:p.Ser402Arg, NP_001158016.1:p.Ser402Arg, NP_001158014.1:p.Ser402Arg, NP_001158011.1:p.Ser402Arg, NP_001158017.1:p.Ser402Arg, NP_001158019.1:p.Ser402Arg, NP_001158020.1:p.Ser402Arg, NP_001158018.1:p.Ser402Arg, NP_001158021.1:p.Ser402Arg, NP_001012977.1:p.Ser402Arg, NP_001158023.1:p.Ser402Arg, NP_001158028.1:p.Ser52Arg
                    10.

                    rs1463414572 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>T [Show Flanks]
                      Chromosome:
                      1:231694678 (GRCh38)
                      1:231830424 (GRCh37)
                      Canonical SPDI:
                      NC_000001.11:231694677:C:T
                      Gene:
                      DISC1 (Varview), TSNAX-DISC1 (Varview)
                      Functional Consequence:
                      non_coding_transcript_variant,missense_variant,coding_sequence_variant,intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      T=0.000028/1 (ALFA)
                      T=0.000023/6 (TOPMED)
                      T=0.000036/5 (GnomAD)
                      HGVS:
                      NC_000001.11:g.231694678C>T, NC_000001.10:g.231830424C>T, NG_011681.2:g.72864C>T, NM_018662.3:c.920C>T, NM_018662.2:c.920C>T, NM_001164537.2:c.920C>T, NM_001164537.1:c.920C>T, NM_001012957.2:c.920C>T, NM_001012957.1:c.920C>T, NM_001164540.2:c.920C>T, NM_001164540.1:c.920C>T, NM_001164538.2:c.920C>T, NM_001164538.1:c.920C>T, NM_001164541.2:c.920C>T, NM_001164541.1:c.920C>T, NM_001164550.2:c.920C>T, NM_001164550.1:c.920C>T, NM_001164552.2:c.920C>T, NM_001164552.1:c.920C>T, NM_001164544.2:c.920C>T, NM_001164544.1:c.920C>T, NM_001164542.2:c.920C>T, NM_001164542.1:c.920C>T, NM_001164553.2:c.920C>T, NM_001164553.1:c.920C>T, NM_001164539.2:c.920C>T, NM_001164539.1:c.920C>T, NM_001012958.2:c.920C>T, NM_001012958.1:c.920C>T, NM_001164545.2:c.920C>T, NM_001164545.1:c.920C>T, NM_001164547.2:c.920C>T, NM_001164547.1:c.920C>T, NM_001164548.2:c.920C>T, NM_001164548.1:c.920C>T, NM_001164546.2:c.920C>T, NM_001164546.1:c.920C>T, NM_001164549.2:c.920C>T, NM_001164549.1:c.920C>T, NM_001012959.2:c.920C>T, NM_001012959.1:c.920C>T, NM_001164551.2:c.920C>T, NM_001164551.1:c.920C>T, NM_001164554.2:c.920C>T, NM_001164554.1:c.920C>T, NM_001164555.2:c.920C>T, NM_001164555.1:c.920C>T, NR_028393.1:n.1641C>T, NR_028394.1:n.1769C>T, NR_028395.1:n.1769C>T, NR_028396.1:n.1641C>T, NR_028397.1:n.1506C>T, NR_028398.1:n.1260C>T, NR_028399.1:n.1876C>T, NR_028400.1:n.1748C>T, NP_061132.2:p.Pro307Leu, NP_001158009.1:p.Pro307Leu, NP_001012975.1:p.Pro307Leu, NP_001158012.1:p.Pro307Leu, NP_001158010.1:p.Pro307Leu, NP_001158013.1:p.Pro307Leu, NP_001158022.1:p.Pro307Leu, NP_001158024.1:p.Pro307Leu, NP_001158016.1:p.Pro307Leu, NP_001158014.1:p.Pro307Leu, NP_001158025.1:p.Pro307Leu, NP_001158011.1:p.Pro307Leu, NP_001012976.1:p.Pro307Leu, NP_001158017.1:p.Pro307Leu, NP_001158019.1:p.Pro307Leu, NP_001158020.1:p.Pro307Leu, NP_001158018.1:p.Pro307Leu, NP_001158021.1:p.Pro307Leu, NP_001012977.1:p.Pro307Leu, NP_001158023.1:p.Pro307Leu, NP_001158026.1:p.Pro307Leu, NP_001158027.1:p.Pro307Leu
                      11.

                      rs1461578163 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        T>A [Show Flanks]
                        Chromosome:
                        1:231694130 (GRCh38)
                        1:231829876 (GRCh37)
                        Canonical SPDI:
                        NC_000001.11:231694129:T:A
                        Gene:
                        DISC1 (Varview), TSNAX-DISC1 (Varview)
                        Functional Consequence:
                        non_coding_transcript_variant,synonymous_variant,coding_sequence_variant,intron_variant
                        Validated:
                        by frequency
                        MAF:
                        A=0.000004/1 (GnomAD_exomes)
                        HGVS:
                        NC_000001.11:g.231694130T>A, NC_000001.10:g.231829876T>A, NG_011681.2:g.72316T>A, NM_018662.3:c.372T>A, NM_018662.2:c.372T>A, NM_001164537.2:c.372T>A, NM_001164537.1:c.372T>A, NM_001012957.2:c.372T>A, NM_001012957.1:c.372T>A, NM_001164540.2:c.372T>A, NM_001164540.1:c.372T>A, NM_001164538.2:c.372T>A, NM_001164538.1:c.372T>A, NM_001164541.2:c.372T>A, NM_001164541.1:c.372T>A, NM_001164550.2:c.372T>A, NM_001164550.1:c.372T>A, NM_001164552.2:c.372T>A, NM_001164552.1:c.372T>A, NM_001164544.2:c.372T>A, NM_001164544.1:c.372T>A, NM_001164542.2:c.372T>A, NM_001164542.1:c.372T>A, NM_001164553.2:c.372T>A, NM_001164553.1:c.372T>A, NM_001164539.2:c.372T>A, NM_001164539.1:c.372T>A, NM_001012958.2:c.372T>A, NM_001012958.1:c.372T>A, NM_001164545.2:c.372T>A, NM_001164545.1:c.372T>A, NM_001164547.2:c.372T>A, NM_001164547.1:c.372T>A, NM_001164548.2:c.372T>A, NM_001164548.1:c.372T>A, NM_001164546.2:c.372T>A, NM_001164546.1:c.372T>A, NM_001164549.2:c.372T>A, NM_001164549.1:c.372T>A, NM_001012959.2:c.372T>A, NM_001012959.1:c.372T>A, NM_001164551.2:c.372T>A, NM_001164551.1:c.372T>A, NM_001164554.2:c.372T>A, NM_001164554.1:c.372T>A, NM_001164555.2:c.372T>A, NM_001164555.1:c.372T>A, NR_028393.1:n.1093T>A, NR_028394.1:n.1221T>A, NR_028395.1:n.1221T>A, NR_028396.1:n.1093T>A, NR_028397.1:n.958T>A, NR_028398.1:n.712T>A, NR_028399.1:n.1328T>A, NR_028400.1:n.1200T>A
                        12.

                        rs1452775697 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          1:231694294 (GRCh38)
                          1:231830040 (GRCh37)
                          Canonical SPDI:
                          NC_000001.11:231694293:C:T
                          Gene:
                          DISC1 (Varview), TSNAX-DISC1 (Varview)
                          Functional Consequence:
                          coding_sequence_variant,intron_variant,missense_variant,non_coding_transcript_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          T=0.000047/1 (ALFA)
                          T=0.000004/1 (GnomAD_exomes)
                          HGVS:
                          NC_000001.11:g.231694294C>T, NC_000001.10:g.231830040C>T, NG_011681.2:g.72480C>T, NM_018662.3:c.536C>T, NM_018662.2:c.536C>T, NM_001164537.2:c.536C>T, NM_001164537.1:c.536C>T, NM_001012957.2:c.536C>T, NM_001012957.1:c.536C>T, NM_001164540.2:c.536C>T, NM_001164540.1:c.536C>T, NM_001164538.2:c.536C>T, NM_001164538.1:c.536C>T, NM_001164541.2:c.536C>T, NM_001164541.1:c.536C>T, NM_001164550.2:c.536C>T, NM_001164550.1:c.536C>T, NM_001164552.2:c.536C>T, NM_001164552.1:c.536C>T, NM_001164544.2:c.536C>T, NM_001164544.1:c.536C>T, NM_001164542.2:c.536C>T, NM_001164542.1:c.536C>T, NM_001164553.2:c.536C>T, NM_001164553.1:c.536C>T, NM_001164539.2:c.536C>T, NM_001164539.1:c.536C>T, NM_001012958.2:c.536C>T, NM_001012958.1:c.536C>T, NM_001164545.2:c.536C>T, NM_001164545.1:c.536C>T, NM_001164547.2:c.536C>T, NM_001164547.1:c.536C>T, NM_001164548.2:c.536C>T, NM_001164548.1:c.536C>T, NM_001164546.2:c.536C>T, NM_001164546.1:c.536C>T, NM_001164549.2:c.536C>T, NM_001164549.1:c.536C>T, NM_001012959.2:c.536C>T, NM_001012959.1:c.536C>T, NM_001164551.2:c.536C>T, NM_001164551.1:c.536C>T, NM_001164554.2:c.536C>T, NM_001164554.1:c.536C>T, NM_001164555.2:c.536C>T, NM_001164555.1:c.536C>T, NR_028393.1:n.1257C>T, NR_028394.1:n.1385C>T, NR_028395.1:n.1385C>T, NR_028396.1:n.1257C>T, NR_028397.1:n.1122C>T, NR_028398.1:n.876C>T, NR_028399.1:n.1492C>T, NR_028400.1:n.1364C>T, NP_061132.2:p.Ser179Leu, NP_001158009.1:p.Ser179Leu, NP_001012975.1:p.Ser179Leu, NP_001158012.1:p.Ser179Leu, NP_001158010.1:p.Ser179Leu, NP_001158013.1:p.Ser179Leu, NP_001158022.1:p.Ser179Leu, NP_001158024.1:p.Ser179Leu, NP_001158016.1:p.Ser179Leu, NP_001158014.1:p.Ser179Leu, NP_001158025.1:p.Ser179Leu, NP_001158011.1:p.Ser179Leu, NP_001012976.1:p.Ser179Leu, NP_001158017.1:p.Ser179Leu, NP_001158019.1:p.Ser179Leu, NP_001158020.1:p.Ser179Leu, NP_001158018.1:p.Ser179Leu, NP_001158021.1:p.Ser179Leu, NP_001012977.1:p.Ser179Leu, NP_001158023.1:p.Ser179Leu, NP_001158026.1:p.Ser179Leu, NP_001158027.1:p.Ser179Leu
                          13.

                          rs1452642173 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>A,C [Show Flanks]
                            Chromosome:
                            1:231701970 (GRCh38)
                            1:231837716 (GRCh37)
                            Canonical SPDI:
                            NC_000001.11:231701969:T:A,NC_000001.11:231701969:T:C
                            Gene:
                            DISC1 (Varview), TSNAX-DISC1 (Varview)
                            Functional Consequence:
                            coding_sequence_variant,non_coding_transcript_variant,intron_variant,synonymous_variant,missense_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            C=0./0 (ALFA)
                            HGVS:
                            NC_000001.11:g.231701970T>A, NC_000001.11:g.231701970T>C, NC_000001.10:g.231837716T>A, NC_000001.10:g.231837716T>C, NG_011681.2:g.80156T>A, NG_011681.2:g.80156T>C, NM_018662.3:c.1063T>A, NM_018662.3:c.1063T>C, NM_018662.2:c.1063T>A, NM_018662.2:c.1063T>C, NM_001164537.2:c.1063T>A, NM_001164537.2:c.1063T>C, NM_001164537.1:c.1063T>A, NM_001164537.1:c.1063T>C, NM_001012957.2:c.1063T>A, NM_001012957.2:c.1063T>C, NM_001012957.1:c.1063T>A, NM_001012957.1:c.1063T>C, NM_001164540.2:c.1063T>A, NM_001164540.2:c.1063T>C, NM_001164540.1:c.1063T>A, NM_001164540.1:c.1063T>C, NM_001164538.2:c.1063T>A, NM_001164538.2:c.1063T>C, NM_001164538.1:c.1063T>A, NM_001164538.1:c.1063T>C, NM_001164541.2:c.1063T>A, NM_001164541.2:c.1063T>C, NM_001164541.1:c.1063T>A, NM_001164541.1:c.1063T>C, NM_001164550.2:c.1063T>A, NM_001164550.2:c.1063T>C, NM_001164550.1:c.1063T>A, NM_001164550.1:c.1063T>C, NM_001164552.2:c.1063T>A, NM_001164552.2:c.1063T>C, NM_001164552.1:c.1063T>A, NM_001164552.1:c.1063T>C, NM_001164544.2:c.1063T>A, NM_001164544.2:c.1063T>C, NM_001164544.1:c.1063T>A, NM_001164544.1:c.1063T>C, NM_001164542.2:c.1063T>A, NM_001164542.2:c.1063T>C, NM_001164542.1:c.1063T>A, NM_001164542.1:c.1063T>C, NM_001164553.2:c.1063T>A, NM_001164553.2:c.1063T>C, NM_001164553.1:c.1063T>A, NM_001164553.1:c.1063T>C, NM_001164539.2:c.1063T>A, NM_001164539.2:c.1063T>C, NM_001164539.1:c.1063T>A, NM_001164539.1:c.1063T>C, NM_001164545.2:c.1063T>A, NM_001164545.2:c.1063T>C, NM_001164545.1:c.1063T>A, NM_001164545.1:c.1063T>C, NM_001164547.2:c.1063T>A, NM_001164547.2:c.1063T>C, NM_001164547.1:c.1063T>A, NM_001164547.1:c.1063T>C, NM_001164548.2:c.1063T>A, NM_001164548.2:c.1063T>C, NM_001164548.1:c.1063T>A, NM_001164548.1:c.1063T>C, NM_001164546.2:c.1063T>A, NM_001164546.2:c.1063T>C, NM_001164546.1:c.1063T>A, NM_001164546.1:c.1063T>C, NM_001164549.2:c.1063T>A, NM_001164549.2:c.1063T>C, NM_001164549.1:c.1063T>A, NM_001164549.1:c.1063T>C, NM_001012959.2:c.1063T>A, NM_001012959.2:c.1063T>C, NM_001012959.1:c.1063T>A, NM_001012959.1:c.1063T>C, NM_001164551.2:c.1063T>A, NM_001164551.2:c.1063T>C, NM_001164551.1:c.1063T>A, NM_001164551.1:c.1063T>C, NM_001164554.2:c.1063T>A, NM_001164554.2:c.1063T>C, NM_001164554.1:c.1063T>A, NM_001164554.1:c.1063T>C, NR_028393.1:n.1784T>A, NR_028393.1:n.1784T>C, NR_028394.1:n.1912T>A, NR_028394.1:n.1912T>C, NR_028395.1:n.1912T>A, NR_028395.1:n.1912T>C, NR_028396.1:n.1784T>A, NR_028396.1:n.1784T>C, NR_028397.1:n.1649T>A, NR_028397.1:n.1649T>C, NR_028398.1:n.1403T>A, NR_028398.1:n.1403T>C, NR_028399.1:n.2019T>A, NR_028399.1:n.2019T>C, NM_025068.1:c.*287T>A, NM_025068.1:c.*287T>C, NM_001039383.1:c.*287T>A, NM_001039383.1:c.*287T>C, NM_001012992.1:c.*287T>A, NM_001012992.1:c.*287T>C, NP_061132.2:p.Leu355Ile, NP_001158009.1:p.Leu355Ile, NP_001012975.1:p.Leu355Ile, NP_001158012.1:p.Leu355Ile, NP_001158010.1:p.Leu355Ile, NP_001158013.1:p.Leu355Ile, NP_001158022.1:p.Leu355Ile, NP_001158024.1:p.Leu355Ile, NP_001158016.1:p.Leu355Ile, NP_001158014.1:p.Leu355Ile, NP_001158025.1:p.Leu355Ile, NP_001158011.1:p.Leu355Ile, NP_001158017.1:p.Leu355Ile, NP_001158019.1:p.Leu355Ile, NP_001158020.1:p.Leu355Ile, NP_001158018.1:p.Leu355Ile, NP_001158021.1:p.Leu355Ile, NP_001012977.1:p.Leu355Ile, NP_001158023.1:p.Leu355Ile, NP_001158026.1:p.Leu355Ile
                            14.

                            rs1452115713 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>C [Show Flanks]
                              Chromosome:
                              1:231693950 (GRCh38)
                              1:231829696 (GRCh37)
                              Canonical SPDI:
                              NC_000001.11:231693949:G:C
                              Gene:
                              DISC1 (Varview), TSNAX-DISC1 (Varview)
                              Functional Consequence:
                              coding_sequence_variant,intron_variant,non_coding_transcript_variant,synonymous_variant
                              Validated:
                              by frequency
                              MAF:
                              C=0.000008/2 (GnomAD_exomes)
                              HGVS:
                              NC_000001.11:g.231693950G>C, NC_000001.10:g.231829696G>C, NG_011681.2:g.72136G>C, NM_018662.3:c.192G>C, NM_018662.2:c.192G>C, NM_001164537.2:c.192G>C, NM_001164537.1:c.192G>C, NM_001012957.2:c.192G>C, NM_001012957.1:c.192G>C, NM_001164540.2:c.192G>C, NM_001164540.1:c.192G>C, NM_001164538.2:c.192G>C, NM_001164538.1:c.192G>C, NM_001164541.2:c.192G>C, NM_001164541.1:c.192G>C, NM_001164550.2:c.192G>C, NM_001164550.1:c.192G>C, NM_001164552.2:c.192G>C, NM_001164552.1:c.192G>C, NM_001164544.2:c.192G>C, NM_001164544.1:c.192G>C, NM_001164542.2:c.192G>C, NM_001164542.1:c.192G>C, NM_001164553.2:c.192G>C, NM_001164553.1:c.192G>C, NM_001164539.2:c.192G>C, NM_001164539.1:c.192G>C, NM_001012958.2:c.192G>C, NM_001012958.1:c.192G>C, NM_001164545.2:c.192G>C, NM_001164545.1:c.192G>C, NM_001164547.2:c.192G>C, NM_001164547.1:c.192G>C, NM_001164548.2:c.192G>C, NM_001164548.1:c.192G>C, NM_001164546.2:c.192G>C, NM_001164546.1:c.192G>C, NM_001164549.2:c.192G>C, NM_001164549.1:c.192G>C, NM_001012959.2:c.192G>C, NM_001012959.1:c.192G>C, NM_001164551.2:c.192G>C, NM_001164551.1:c.192G>C, NM_001164554.2:c.192G>C, NM_001164554.1:c.192G>C, NM_001164555.2:c.192G>C, NM_001164555.1:c.192G>C, NR_028393.1:n.913G>C, NR_028394.1:n.1041G>C, NR_028395.1:n.1041G>C, NR_028396.1:n.913G>C, NR_028397.1:n.778G>C, NR_028398.1:n.532G>C, NR_028399.1:n.1148G>C, NR_028400.1:n.1020G>C
                              15.

                              rs1450009486 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                1:231694075 (GRCh38)
                                1:231829821 (GRCh37)
                                Canonical SPDI:
                                NC_000001.11:231694074:C:T
                                Gene:
                                DISC1 (Varview), TSNAX-DISC1 (Varview)
                                Functional Consequence:
                                non_coding_transcript_variant,coding_sequence_variant,missense_variant,intron_variant
                                Validated:
                                by frequency
                                MAF:
                                T=0.000004/1 (GnomAD_exomes)
                                HGVS:
                                NC_000001.11:g.231694075C>T, NC_000001.10:g.231829821C>T, NG_011681.2:g.72261C>T, NM_018662.3:c.317C>T, NM_018662.2:c.317C>T, NM_001164537.2:c.317C>T, NM_001164537.1:c.317C>T, NM_001012957.2:c.317C>T, NM_001012957.1:c.317C>T, NM_001164540.2:c.317C>T, NM_001164540.1:c.317C>T, NM_001164538.2:c.317C>T, NM_001164538.1:c.317C>T, NM_001164541.2:c.317C>T, NM_001164541.1:c.317C>T, NM_001164550.2:c.317C>T, NM_001164550.1:c.317C>T, NM_001164552.2:c.317C>T, NM_001164552.1:c.317C>T, NM_001164544.2:c.317C>T, NM_001164544.1:c.317C>T, NM_001164542.2:c.317C>T, NM_001164542.1:c.317C>T, NM_001164553.2:c.317C>T, NM_001164553.1:c.317C>T, NM_001164539.2:c.317C>T, NM_001164539.1:c.317C>T, NM_001012958.2:c.317C>T, NM_001012958.1:c.317C>T, NM_001164545.2:c.317C>T, NM_001164545.1:c.317C>T, NM_001164547.2:c.317C>T, NM_001164547.1:c.317C>T, NM_001164548.2:c.317C>T, NM_001164548.1:c.317C>T, NM_001164546.2:c.317C>T, NM_001164546.1:c.317C>T, NM_001164549.2:c.317C>T, NM_001164549.1:c.317C>T, NM_001012959.2:c.317C>T, NM_001012959.1:c.317C>T, NM_001164551.2:c.317C>T, NM_001164551.1:c.317C>T, NM_001164554.2:c.317C>T, NM_001164554.1:c.317C>T, NM_001164555.2:c.317C>T, NM_001164555.1:c.317C>T, NR_028393.1:n.1038C>T, NR_028394.1:n.1166C>T, NR_028395.1:n.1166C>T, NR_028396.1:n.1038C>T, NR_028397.1:n.903C>T, NR_028398.1:n.657C>T, NR_028399.1:n.1273C>T, NR_028400.1:n.1145C>T, NP_061132.2:p.Pro106Leu, NP_001158009.1:p.Pro106Leu, NP_001012975.1:p.Pro106Leu, NP_001158012.1:p.Pro106Leu, NP_001158010.1:p.Pro106Leu, NP_001158013.1:p.Pro106Leu, NP_001158022.1:p.Pro106Leu, NP_001158024.1:p.Pro106Leu, NP_001158016.1:p.Pro106Leu, NP_001158014.1:p.Pro106Leu, NP_001158025.1:p.Pro106Leu, NP_001158011.1:p.Pro106Leu, NP_001012976.1:p.Pro106Leu, NP_001158017.1:p.Pro106Leu, NP_001158019.1:p.Pro106Leu, NP_001158020.1:p.Pro106Leu, NP_001158018.1:p.Pro106Leu, NP_001158021.1:p.Pro106Leu, NP_001012977.1:p.Pro106Leu, NP_001158023.1:p.Pro106Leu, NP_001158026.1:p.Pro106Leu, NP_001158027.1:p.Pro106Leu
                                16.

                                rs1448401085 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>T [Show Flanks]
                                  Chromosome:
                                  1:231626917 (GRCh38)
                                  1:231762663 (GRCh37)
                                  Canonical SPDI:
                                  NC_000001.11:231626916:G:T
                                  Gene:
                                  DISC1 (Varview), TSNAX-DISC1 (Varview)
                                  Functional Consequence:
                                  coding_sequence_variant,missense_variant,intron_variant
                                  Validated:
                                  by frequency
                                  MAF:
                                  T=0.00001/1 (GnomAD_exomes)
                                  HGVS:
                                  NC_000001.11:g.231626917G>T, NC_000001.10:g.231762663G>T, NG_011681.2:g.5103G>T, NM_018662.3:c.50G>T, NM_018662.2:c.50G>T, NM_001164537.2:c.50G>T, NM_001164537.1:c.50G>T, NM_001012957.2:c.50G>T, NM_001012957.1:c.50G>T, NM_001164540.2:c.50G>T, NM_001164540.1:c.50G>T, NM_001164538.2:c.50G>T, NM_001164538.1:c.50G>T, NM_001164541.2:c.50G>T, NM_001164541.1:c.50G>T, NM_001164550.2:c.50G>T, NM_001164550.1:c.50G>T, NM_001164552.2:c.50G>T, NM_001164552.1:c.50G>T, NM_001164544.2:c.50G>T, NM_001164544.1:c.50G>T, NM_001164542.2:c.50G>T, NM_001164542.1:c.50G>T, NM_001164553.2:c.50G>T, NM_001164553.1:c.50G>T, NM_001164539.2:c.50G>T, NM_001164539.1:c.50G>T, NM_001012958.2:c.50G>T, NM_001012958.1:c.50G>T, NM_001164545.2:c.50G>T, NM_001164545.1:c.50G>T, NM_001164547.2:c.50G>T, NM_001164547.1:c.50G>T, NM_001164548.2:c.50G>T, NM_001164548.1:c.50G>T, NM_001164546.2:c.50G>T, NM_001164546.1:c.50G>T, NM_001164549.2:c.50G>T, NM_001164549.1:c.50G>T, NM_001012959.2:c.50G>T, NM_001012959.1:c.50G>T, NM_001164551.2:c.50G>T, NM_001164551.1:c.50G>T, NM_001164554.2:c.50G>T, NM_001164554.1:c.50G>T, NM_001164555.2:c.50G>T, NM_001164555.1:c.50G>T, NM_001164556.2:c.50G>T, NM_001164556.1:c.50G>T, NP_061132.2:p.Gly17Val, NP_001158009.1:p.Gly17Val, NP_001012975.1:p.Gly17Val, NP_001158012.1:p.Gly17Val, NP_001158010.1:p.Gly17Val, NP_001158013.1:p.Gly17Val, NP_001158022.1:p.Gly17Val, NP_001158024.1:p.Gly17Val, NP_001158016.1:p.Gly17Val, NP_001158014.1:p.Gly17Val, NP_001158025.1:p.Gly17Val, NP_001158011.1:p.Gly17Val, NP_001012976.1:p.Gly17Val, NP_001158017.1:p.Gly17Val, NP_001158019.1:p.Gly17Val, NP_001158020.1:p.Gly17Val, NP_001158018.1:p.Gly17Val, NP_001158021.1:p.Gly17Val, NP_001012977.1:p.Gly17Val, NP_001158023.1:p.Gly17Val, NP_001158026.1:p.Gly17Val, NP_001158027.1:p.Gly17Val, NP_001158028.1:p.Gly17Val
                                  17.

                                  rs1441735094 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>G [Show Flanks]
                                    Chromosome:
                                    1:231694285 (GRCh38)
                                    1:231830031 (GRCh37)
                                    Canonical SPDI:
                                    NC_000001.11:231694284:C:G
                                    Gene:
                                    DISC1 (Varview), TSNAX-DISC1 (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,missense_variant,non_coding_transcript_variant,intron_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_000001.11:g.231694285C>G, NC_000001.10:g.231830031C>G, NG_011681.2:g.72471C>G, NM_018662.3:c.527C>G, NM_018662.2:c.527C>G, NM_001164537.2:c.527C>G, NM_001164537.1:c.527C>G, NM_001012957.2:c.527C>G, NM_001012957.1:c.527C>G, NM_001164540.2:c.527C>G, NM_001164540.1:c.527C>G, NM_001164538.2:c.527C>G, NM_001164538.1:c.527C>G, NM_001164541.2:c.527C>G, NM_001164541.1:c.527C>G, NM_001164550.2:c.527C>G, NM_001164550.1:c.527C>G, NM_001164552.2:c.527C>G, NM_001164552.1:c.527C>G, NM_001164544.2:c.527C>G, NM_001164544.1:c.527C>G, NM_001164542.2:c.527C>G, NM_001164542.1:c.527C>G, NM_001164553.2:c.527C>G, NM_001164553.1:c.527C>G, NM_001164539.2:c.527C>G, NM_001164539.1:c.527C>G, NM_001012958.2:c.527C>G, NM_001012958.1:c.527C>G, NM_001164545.2:c.527C>G, NM_001164545.1:c.527C>G, NM_001164547.2:c.527C>G, NM_001164547.1:c.527C>G, NM_001164548.2:c.527C>G, NM_001164548.1:c.527C>G, NM_001164546.2:c.527C>G, NM_001164546.1:c.527C>G, NM_001164549.2:c.527C>G, NM_001164549.1:c.527C>G, NM_001012959.2:c.527C>G, NM_001012959.1:c.527C>G, NM_001164551.2:c.527C>G, NM_001164551.1:c.527C>G, NM_001164554.2:c.527C>G, NM_001164554.1:c.527C>G, NM_001164555.2:c.527C>G, NM_001164555.1:c.527C>G, NR_028393.1:n.1248C>G, NR_028394.1:n.1376C>G, NR_028395.1:n.1376C>G, NR_028396.1:n.1248C>G, NR_028397.1:n.1113C>G, NR_028398.1:n.867C>G, NR_028399.1:n.1483C>G, NR_028400.1:n.1355C>G, NP_061132.2:p.Ser176Cys, NP_001158009.1:p.Ser176Cys, NP_001012975.1:p.Ser176Cys, NP_001158012.1:p.Ser176Cys, NP_001158010.1:p.Ser176Cys, NP_001158013.1:p.Ser176Cys, NP_001158022.1:p.Ser176Cys, NP_001158024.1:p.Ser176Cys, NP_001158016.1:p.Ser176Cys, NP_001158014.1:p.Ser176Cys, NP_001158025.1:p.Ser176Cys, NP_001158011.1:p.Ser176Cys, NP_001012976.1:p.Ser176Cys, NP_001158017.1:p.Ser176Cys, NP_001158019.1:p.Ser176Cys, NP_001158020.1:p.Ser176Cys, NP_001158018.1:p.Ser176Cys, NP_001158021.1:p.Ser176Cys, NP_001012977.1:p.Ser176Cys, NP_001158023.1:p.Ser176Cys, NP_001158026.1:p.Ser176Cys, NP_001158027.1:p.Ser176Cys
                                    18.

                                    rs1441696929 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      1:231626895 (GRCh38)
                                      1:231762641 (GRCh37)
                                      Canonical SPDI:
                                      NC_000001.11:231626894:C:T
                                      Gene:
                                      DISC1 (Varview), TSNAX-DISC1 (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,missense_variant,intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0./0 (ALFA)
                                      T=0.000004/1 (TOPMED)
                                      T=0.000007/1 (GnomAD)
                                      HGVS:
                                      NC_000001.11:g.231626895C>T, NC_000001.10:g.231762641C>T, NG_011681.2:g.5081C>T, NM_018662.3:c.28C>T, NM_018662.2:c.28C>T, NM_001164537.2:c.28C>T, NM_001164537.1:c.28C>T, NM_001012957.2:c.28C>T, NM_001012957.1:c.28C>T, NM_001164540.2:c.28C>T, NM_001164540.1:c.28C>T, NM_001164538.2:c.28C>T, NM_001164538.1:c.28C>T, NM_001164541.2:c.28C>T, NM_001164541.1:c.28C>T, NM_001164550.2:c.28C>T, NM_001164550.1:c.28C>T, NM_001164552.2:c.28C>T, NM_001164552.1:c.28C>T, NM_001164544.2:c.28C>T, NM_001164544.1:c.28C>T, NM_001164542.2:c.28C>T, NM_001164542.1:c.28C>T, NM_001164553.2:c.28C>T, NM_001164553.1:c.28C>T, NM_001164539.2:c.28C>T, NM_001164539.1:c.28C>T, NM_001012958.2:c.28C>T, NM_001012958.1:c.28C>T, NM_001164545.2:c.28C>T, NM_001164545.1:c.28C>T, NM_001164547.2:c.28C>T, NM_001164547.1:c.28C>T, NM_001164548.2:c.28C>T, NM_001164548.1:c.28C>T, NM_001164546.2:c.28C>T, NM_001164546.1:c.28C>T, NM_001164549.2:c.28C>T, NM_001164549.1:c.28C>T, NM_001012959.2:c.28C>T, NM_001012959.1:c.28C>T, NM_001164551.2:c.28C>T, NM_001164551.1:c.28C>T, NM_001164554.2:c.28C>T, NM_001164554.1:c.28C>T, NM_001164555.2:c.28C>T, NM_001164555.1:c.28C>T, NM_001164556.2:c.28C>T, NM_001164556.1:c.28C>T, NP_061132.2:p.Pro10Ser, NP_001158009.1:p.Pro10Ser, NP_001012975.1:p.Pro10Ser, NP_001158012.1:p.Pro10Ser, NP_001158010.1:p.Pro10Ser, NP_001158013.1:p.Pro10Ser, NP_001158022.1:p.Pro10Ser, NP_001158024.1:p.Pro10Ser, NP_001158016.1:p.Pro10Ser, NP_001158014.1:p.Pro10Ser, NP_001158025.1:p.Pro10Ser, NP_001158011.1:p.Pro10Ser, NP_001012976.1:p.Pro10Ser, NP_001158017.1:p.Pro10Ser, NP_001158019.1:p.Pro10Ser, NP_001158020.1:p.Pro10Ser, NP_001158018.1:p.Pro10Ser, NP_001158021.1:p.Pro10Ser, NP_001012977.1:p.Pro10Ser, NP_001158023.1:p.Pro10Ser, NP_001158026.1:p.Pro10Ser, NP_001158027.1:p.Pro10Ser, NP_001158028.1:p.Pro10Ser
                                      19.

                                      rs1440933409 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>A [Show Flanks]
                                        Chromosome:
                                        1:231694427 (GRCh38)
                                        1:231830173 (GRCh37)
                                        Canonical SPDI:
                                        NC_000001.11:231694426:T:A
                                        Gene:
                                        DISC1 (Varview), TSNAX-DISC1 (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,synonymous_variant,non_coding_transcript_variant,intron_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        A=0./0 (ALFA)
                                        A=0.000004/1 (TOPMED)
                                        HGVS:
                                        NC_000001.11:g.231694427T>A, NC_000001.10:g.231830173T>A, NG_011681.2:g.72613T>A, NM_018662.3:c.669T>A, NM_018662.2:c.669T>A, NM_001164537.2:c.669T>A, NM_001164537.1:c.669T>A, NM_001012957.2:c.669T>A, NM_001012957.1:c.669T>A, NM_001164540.2:c.669T>A, NM_001164540.1:c.669T>A, NM_001164538.2:c.669T>A, NM_001164538.1:c.669T>A, NM_001164541.2:c.669T>A, NM_001164541.1:c.669T>A, NM_001164550.2:c.669T>A, NM_001164550.1:c.669T>A, NM_001164552.2:c.669T>A, NM_001164552.1:c.669T>A, NM_001164544.2:c.669T>A, NM_001164544.1:c.669T>A, NM_001164542.2:c.669T>A, NM_001164542.1:c.669T>A, NM_001164553.2:c.669T>A, NM_001164553.1:c.669T>A, NM_001164539.2:c.669T>A, NM_001164539.1:c.669T>A, NM_001012958.2:c.669T>A, NM_001012958.1:c.669T>A, NM_001164545.2:c.669T>A, NM_001164545.1:c.669T>A, NM_001164547.2:c.669T>A, NM_001164547.1:c.669T>A, NM_001164548.2:c.669T>A, NM_001164548.1:c.669T>A, NM_001164546.2:c.669T>A, NM_001164546.1:c.669T>A, NM_001164549.2:c.669T>A, NM_001164549.1:c.669T>A, NM_001012959.2:c.669T>A, NM_001012959.1:c.669T>A, NM_001164551.2:c.669T>A, NM_001164551.1:c.669T>A, NM_001164554.2:c.669T>A, NM_001164554.1:c.669T>A, NM_001164555.2:c.669T>A, NM_001164555.1:c.669T>A, NR_028393.1:n.1390T>A, NR_028394.1:n.1518T>A, NR_028395.1:n.1518T>A, NR_028396.1:n.1390T>A, NR_028397.1:n.1255T>A, NR_028398.1:n.1009T>A, NR_028399.1:n.1625T>A, NR_028400.1:n.1497T>A
                                        20.

                                        rs1440050362 [Homo sapiens]
                                          Variant type:
                                          DEL
                                          Alleles:
                                          GC>- [Show Flanks]
                                          Chromosome:
                                          1:231694132 (GRCh38)
                                          1:231829878 (GRCh37)
                                          Canonical SPDI:
                                          NC_000001.11:231694131:GC:
                                          Gene:
                                          DISC1 (Varview), TSNAX-DISC1 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,frameshift_variant,non_coding_transcript_variant,intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          -=0./0 (ALFA)
                                          -=0.000007/1 (GnomAD)
                                          -=0.000008/2 (TOPMED)
                                          HGVS:
                                          NC_000001.11:g.231694132_231694133del, NC_000001.10:g.231829878_231829879del, NG_011681.2:g.72318_72319del, NM_018662.3:c.374_375del, NM_018662.2:c.374_375del, NM_001164537.2:c.374_375del, NM_001164537.1:c.374_375del, NM_001012957.2:c.374_375del, NM_001012957.1:c.374_375del, NM_001164540.2:c.374_375del, NM_001164540.1:c.374_375del, NM_001164538.2:c.374_375del, NM_001164538.1:c.374_375del, NM_001164541.2:c.374_375del, NM_001164541.1:c.374_375del, NM_001164550.2:c.374_375del, NM_001164550.1:c.374_375del, NM_001164552.2:c.374_375del, NM_001164552.1:c.374_375del, NM_001164544.2:c.374_375del, NM_001164544.1:c.374_375del, NM_001164542.2:c.374_375del, NM_001164542.1:c.374_375del, NM_001164553.2:c.374_375del, NM_001164553.1:c.374_375del, NM_001164539.2:c.374_375del, NM_001164539.1:c.374_375del, NM_001012958.2:c.374_375del, NM_001012958.1:c.374_375del, NM_001164545.2:c.374_375del, NM_001164545.1:c.374_375del, NM_001164547.2:c.374_375del, NM_001164547.1:c.374_375del, NM_001164548.2:c.374_375del, NM_001164548.1:c.374_375del, NM_001164546.2:c.374_375del, NM_001164546.1:c.374_375del, NM_001164549.2:c.374_375del, NM_001164549.1:c.374_375del, NM_001012959.2:c.374_375del, NM_001012959.1:c.374_375del, NM_001164551.2:c.374_375del, NM_001164551.1:c.374_375del, NM_001164554.2:c.374_375del, NM_001164554.1:c.374_375del, NM_001164555.2:c.374_375del, NM_001164555.1:c.374_375del, NR_028393.1:n.1095_1096del, NR_028394.1:n.1223_1224del, NR_028395.1:n.1223_1224del, NR_028396.1:n.1095_1096del, NR_028397.1:n.960_961del, NR_028398.1:n.714_715del, NR_028399.1:n.1330_1331del, NR_028400.1:n.1202_1203del, NP_061132.2:p.Gly125fs, NP_001158009.1:p.Gly125fs, NP_001012975.1:p.Gly125fs, NP_001158012.1:p.Gly125fs, NP_001158010.1:p.Gly125fs, NP_001158013.1:p.Gly125fs, NP_001158022.1:p.Gly125fs, NP_001158024.1:p.Gly125fs, NP_001158016.1:p.Gly125fs, NP_001158014.1:p.Gly125fs, NP_001158025.1:p.Gly125fs, NP_001158011.1:p.Gly125fs, NP_001012976.1:p.Gly125fs, NP_001158017.1:p.Gly125fs, NP_001158019.1:p.Gly125fs, NP_001158020.1:p.Gly125fs, NP_001158018.1:p.Gly125fs, NP_001158021.1:p.Gly125fs, NP_001012977.1:p.Gly125fs, NP_001158023.1:p.Gly125fs, NP_001158026.1:p.Gly125fs, NP_001158027.1:p.Gly125fs

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