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Items: 1 to 20 of 385

1.

rs1488533333 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    9:132237225 (GRCh38)
    9:135112612 (GRCh37)
    Canonical SPDI:
    NC_000009.12:132237224:C:T
    Gene:
    NTNG2 (Varview)
    Functional Consequence:
    coding_sequence_variant,genic_downstream_transcript_variant,intron_variant,missense_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0./0 (ALFA)
    T=0.000004/1 (TOPMED)
    T=0.000014/2 (GnomAD)
    HGVS:

    2.

    rs1484878913 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ->T [Show Flanks]
      Chromosome:
      9:132198431 (GRCh38)
      9:135073819 (GRCh37)
      Canonical SPDI:
      NC_000009.12:132198431:T:TT
      Gene:
      NTNG2 (Varview)
      Functional Consequence:
      coding_sequence_variant,genic_upstream_transcript_variant,frameshift_variant
      Validated:
      by frequency
      MAF:
      T=0.000004/1 (GnomAD_exomes)
      HGVS:
      NC_000009.12:g.132198432dup, NC_000009.11:g.135073819dup, XM_011519097.4:c.680dup, XM_011519097.3:c.680dup, XM_011519097.2:c.680dup, XM_011519097.1:c.680dup, XM_006717304.4:c.680dup, XM_006717304.3:c.680dup, XM_006717304.2:c.680dup, XM_006717304.1:c.680dup, XM_011519104.4:c.680dup, XM_011519104.3:c.680dup, XM_011519104.2:c.680dup, XM_011519104.1:c.680dup, NM_032536.4:c.680dup, NM_032536.3:c.680dup, NM_032536.2:c.680dup, XM_011519094.3:c.680dup, XM_011519094.2:c.680dup, XM_011519094.1:c.680dup, XM_011519098.3:c.680dup, XM_011519098.2:c.680dup, XM_011519098.1:c.680dup, XM_011519106.3:c.680dup, XM_011519106.2:c.680dup, XM_011519106.1:c.680dup, XM_011519102.3:c.680dup, XM_011519102.2:c.680dup, XM_011519102.1:c.680dup, XM_011519099.3:c.680dup, XM_011519099.2:c.680dup, XM_011519099.1:c.680dup, XM_011519096.3:c.680dup, XM_011519096.2:c.680dup, XM_011519096.1:c.680dup, XM_011519100.3:c.680dup, XM_011519100.2:c.680dup, XM_011519100.1:c.680dup, XM_011519105.3:c.680dup, XM_011519105.2:c.680dup, XM_011519105.1:c.680dup, XM_011519107.3:c.680dup, XM_011519107.2:c.680dup, XM_011519107.1:c.680dup, XM_011519103.3:c.680dup, XM_011519103.2:c.680dup, XM_011519103.1:c.680dup, XM_011519108.3:c.680dup, XM_011519108.2:c.680dup, XM_011519108.1:c.680dup, XM_011519109.3:c.680dup, XM_011519109.2:c.680dup, XM_011519109.1:c.680dup, XM_011519110.3:c.680dup, XM_011519110.2:c.680dup, XM_011519110.1:c.680dup, XM_017015212.2:c.680dup, XM_017015212.1:c.680dup, XM_017015213.2:c.680dup, XM_017015213.1:c.680dup, XM_017015216.2:c.680dup, XM_017015216.1:c.680dup, XM_047423971.1:c.680dup, XM_047423970.1:c.680dup, XP_011517399.1:p.Arg228fs, XP_006717367.1:p.Arg228fs, XP_011517406.1:p.Arg228fs, NP_115925.2:p.Arg228fs, XP_011517396.1:p.Arg228fs, XP_011517400.1:p.Arg228fs, XP_011517408.1:p.Arg228fs, XP_011517404.1:p.Arg228fs, XP_011517401.1:p.Arg228fs, XP_011517398.1:p.Arg228fs, XP_011517402.1:p.Arg228fs, XP_011517407.1:p.Arg228fs, XP_011517409.1:p.Arg228fs, XP_011517405.1:p.Arg228fs, XP_011517410.1:p.Arg228fs, XP_011517411.1:p.Arg228fs, XP_011517412.1:p.Arg228fs, XP_016870701.1:p.Arg228fs, XP_016870702.1:p.Arg228fs, XP_016870705.1:p.Arg228fs, XP_047279927.1:p.Arg228fs, XP_047279926.1:p.Arg228fs

      3.

      rs1483207462 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A,C [Show Flanks]
        Chromosome:
        9:132198363 (GRCh38)
        9:135073750 (GRCh37)
        Canonical SPDI:
        NC_000009.12:132198362:G:A,NC_000009.12:132198362:G:C
        Gene:
        NTNG2 (Varview)
        Functional Consequence:
        coding_sequence_variant,genic_upstream_transcript_variant,missense_variant
        Validated:
        by frequency,by alfa
        MAF:
        C=0.000111/1 (ALFA)
        C=0.000004/1 (GnomAD_exomes)
        HGVS:
        NC_000009.12:g.132198363G>A, NC_000009.12:g.132198363G>C, NC_000009.11:g.135073750G>A, NC_000009.11:g.135073750G>C, XM_011519097.4:c.611G>A, XM_011519097.4:c.611G>C, XM_011519097.3:c.611G>A, XM_011519097.3:c.611G>C, XM_011519097.2:c.611G>A, XM_011519097.2:c.611G>C, XM_011519097.1:c.611G>A, XM_011519097.1:c.611G>C, XM_006717304.4:c.611G>A, XM_006717304.4:c.611G>C, XM_006717304.3:c.611G>A, XM_006717304.3:c.611G>C, XM_006717304.2:c.611G>A, XM_006717304.2:c.611G>C, XM_006717304.1:c.611G>A, XM_006717304.1:c.611G>C, XM_011519104.4:c.611G>A, XM_011519104.4:c.611G>C, XM_011519104.3:c.611G>A, XM_011519104.3:c.611G>C, XM_011519104.2:c.611G>A, XM_011519104.2:c.611G>C, XM_011519104.1:c.611G>A, XM_011519104.1:c.611G>C, NM_032536.4:c.611G>A, NM_032536.4:c.611G>C, NM_032536.3:c.611G>A, NM_032536.3:c.611G>C, NM_032536.2:c.611G>A, NM_032536.2:c.611G>C, XM_011519094.3:c.611G>A, XM_011519094.3:c.611G>C, XM_011519094.2:c.611G>A, XM_011519094.2:c.611G>C, XM_011519094.1:c.611G>A, XM_011519094.1:c.611G>C, XM_011519098.3:c.611G>A, XM_011519098.3:c.611G>C, XM_011519098.2:c.611G>A, XM_011519098.2:c.611G>C, XM_011519098.1:c.611G>A, XM_011519098.1:c.611G>C, XM_011519106.3:c.611G>A, XM_011519106.3:c.611G>C, XM_011519106.2:c.611G>A, XM_011519106.2:c.611G>C, XM_011519106.1:c.611G>A, XM_011519106.1:c.611G>C, XM_011519102.3:c.611G>A, XM_011519102.3:c.611G>C, XM_011519102.2:c.611G>A, XM_011519102.2:c.611G>C, XM_011519102.1:c.611G>A, XM_011519102.1:c.611G>C, XM_011519099.3:c.611G>A, XM_011519099.3:c.611G>C, XM_011519099.2:c.611G>A, XM_011519099.2:c.611G>C, XM_011519099.1:c.611G>A, XM_011519099.1:c.611G>C, XM_011519096.3:c.611G>A, XM_011519096.3:c.611G>C, XM_011519096.2:c.611G>A, XM_011519096.2:c.611G>C, XM_011519096.1:c.611G>A, XM_011519096.1:c.611G>C, XM_011519100.3:c.611G>A, XM_011519100.3:c.611G>C, XM_011519100.2:c.611G>A, XM_011519100.2:c.611G>C, XM_011519100.1:c.611G>A, XM_011519100.1:c.611G>C, XM_011519105.3:c.611G>A, XM_011519105.3:c.611G>C, XM_011519105.2:c.611G>A, XM_011519105.2:c.611G>C, XM_011519105.1:c.611G>A, XM_011519105.1:c.611G>C, XM_011519107.3:c.611G>A, XM_011519107.3:c.611G>C, XM_011519107.2:c.611G>A, XM_011519107.2:c.611G>C, XM_011519107.1:c.611G>A, XM_011519107.1:c.611G>C, XM_011519103.3:c.611G>A, XM_011519103.3:c.611G>C, XM_011519103.2:c.611G>A, XM_011519103.2:c.611G>C, XM_011519103.1:c.611G>A, XM_011519103.1:c.611G>C, XM_011519108.3:c.611G>A, XM_011519108.3:c.611G>C, XM_011519108.2:c.611G>A, XM_011519108.2:c.611G>C, XM_011519108.1:c.611G>A, XM_011519108.1:c.611G>C, XM_011519109.3:c.611G>A, XM_011519109.3:c.611G>C, XM_011519109.2:c.611G>A, XM_011519109.2:c.611G>C, XM_011519109.1:c.611G>A, XM_011519109.1:c.611G>C, XM_011519110.3:c.611G>A, XM_011519110.3:c.611G>C, XM_011519110.2:c.611G>A, XM_011519110.2:c.611G>C, XM_011519110.1:c.611G>A, XM_011519110.1:c.611G>C, XM_017015212.2:c.611G>A, XM_017015212.2:c.611G>C, XM_017015212.1:c.611G>A, XM_017015212.1:c.611G>C, XM_017015213.2:c.611G>A, XM_017015213.2:c.611G>C, XM_017015213.1:c.611G>A, XM_017015213.1:c.611G>C, XM_017015216.2:c.611G>A, XM_017015216.2:c.611G>C, XM_017015216.1:c.611G>A, XM_017015216.1:c.611G>C, XM_047423971.1:c.611G>A, XM_047423971.1:c.611G>C, XM_047423970.1:c.611G>A, XM_047423970.1:c.611G>C, XP_011517399.1:p.Gly204Asp, XP_011517399.1:p.Gly204Ala, XP_006717367.1:p.Gly204Asp, XP_006717367.1:p.Gly204Ala, XP_011517406.1:p.Gly204Asp, XP_011517406.1:p.Gly204Ala, NP_115925.2:p.Gly204Asp, NP_115925.2:p.Gly204Ala, XP_011517396.1:p.Gly204Asp, XP_011517396.1:p.Gly204Ala, XP_011517400.1:p.Gly204Asp, XP_011517400.1:p.Gly204Ala, XP_011517408.1:p.Gly204Asp, XP_011517408.1:p.Gly204Ala, XP_011517404.1:p.Gly204Asp, XP_011517404.1:p.Gly204Ala, XP_011517401.1:p.Gly204Asp, XP_011517401.1:p.Gly204Ala, XP_011517398.1:p.Gly204Asp, XP_011517398.1:p.Gly204Ala, XP_011517402.1:p.Gly204Asp, XP_011517402.1:p.Gly204Ala, XP_011517407.1:p.Gly204Asp, XP_011517407.1:p.Gly204Ala, XP_011517409.1:p.Gly204Asp, XP_011517409.1:p.Gly204Ala, XP_011517405.1:p.Gly204Asp, XP_011517405.1:p.Gly204Ala, XP_011517410.1:p.Gly204Asp, XP_011517410.1:p.Gly204Ala, XP_011517411.1:p.Gly204Asp, XP_011517411.1:p.Gly204Ala, XP_011517412.1:p.Gly204Asp, XP_011517412.1:p.Gly204Ala, XP_016870701.1:p.Gly204Asp, XP_016870701.1:p.Gly204Ala, XP_016870702.1:p.Gly204Asp, XP_016870702.1:p.Gly204Ala, XP_016870705.1:p.Gly204Asp, XP_016870705.1:p.Gly204Ala, XP_047279927.1:p.Gly204Asp, XP_047279927.1:p.Gly204Ala, XP_047279926.1:p.Gly204Asp, XP_047279926.1:p.Gly204Ala

        4.

        rs1482041770 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>T [Show Flanks]
          Chromosome:
          9:132226966 (GRCh38)
          9:135102353 (GRCh37)
          Canonical SPDI:
          NC_000009.12:132226965:C:T
          Gene:
          NTNG2 (Varview)
          Functional Consequence:
          coding_sequence_variant,genic_upstream_transcript_variant,genic_downstream_transcript_variant,synonymous_variant
          HGVS:
          NC_000009.12:g.132226966C>T, NC_000009.11:g.135102353C>T, XM_011519097.4:c.975C>T, XM_011519097.3:c.975C>T, XM_011519097.2:c.975C>T, XM_011519097.1:c.975C>T, XM_006717304.4:c.975C>T, XM_006717304.3:c.975C>T, XM_006717304.2:c.975C>T, XM_006717304.1:c.975C>T, XM_011519104.4:c.975C>T, XM_011519104.3:c.975C>T, XM_011519104.2:c.975C>T, XM_011519104.1:c.975C>T, NM_032536.4:c.975C>T, NM_032536.3:c.975C>T, NM_032536.2:c.975C>T, XM_011519094.3:c.975C>T, XM_011519094.2:c.975C>T, XM_011519094.1:c.975C>T, XM_011519098.3:c.975C>T, XM_011519098.2:c.975C>T, XM_011519098.1:c.975C>T, XM_011519106.3:c.975C>T, XM_011519106.2:c.975C>T, XM_011519106.1:c.975C>T, XM_011519102.3:c.975C>T, XM_011519102.2:c.975C>T, XM_011519102.1:c.975C>T, XM_011519099.3:c.975C>T, XM_011519099.2:c.975C>T, XM_011519099.1:c.975C>T, XM_011519096.3:c.975C>T, XM_011519096.2:c.975C>T, XM_011519096.1:c.975C>T, XM_011519100.3:c.975C>T, XM_011519100.2:c.975C>T, XM_011519100.1:c.975C>T, XM_011519105.3:c.975C>T, XM_011519105.2:c.975C>T, XM_011519105.1:c.975C>T, XM_011519107.3:c.975C>T, XM_011519107.2:c.975C>T, XM_011519107.1:c.975C>T, XM_011519103.3:c.975C>T, XM_011519103.2:c.975C>T, XM_011519103.1:c.975C>T, XM_011519108.3:c.975C>T, XM_011519108.2:c.975C>T, XM_011519108.1:c.975C>T, XM_011519109.3:c.975C>T, XM_011519109.2:c.975C>T, XM_011519109.1:c.975C>T, XM_011519110.3:c.975C>T, XM_011519110.2:c.975C>T, XM_011519110.1:c.975C>T, XM_017015212.2:c.975C>T, XM_017015212.1:c.975C>T, XM_017015213.2:c.975C>T, XM_017015213.1:c.975C>T, XM_047423971.1:c.975C>T, XM_047423970.1:c.975C>T

          5.

          rs1480092180 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>G [Show Flanks]
            Chromosome:
            9:132198317 (GRCh38)
            9:135073704 (GRCh37)
            Canonical SPDI:
            NC_000009.12:132198316:A:G
            Gene:
            NTNG2 (Varview)
            Functional Consequence:
            coding_sequence_variant,genic_upstream_transcript_variant,missense_variant
            Validated:
            by frequency
            MAF:
            G=0.000004/1 (GnomAD_exomes)
            HGVS:
            NC_000009.12:g.132198317A>G, NC_000009.11:g.135073704A>G, XM_011519097.4:c.565A>G, XM_011519097.3:c.565A>G, XM_011519097.2:c.565A>G, XM_011519097.1:c.565A>G, XM_006717304.4:c.565A>G, XM_006717304.3:c.565A>G, XM_006717304.2:c.565A>G, XM_006717304.1:c.565A>G, XM_011519104.4:c.565A>G, XM_011519104.3:c.565A>G, XM_011519104.2:c.565A>G, XM_011519104.1:c.565A>G, NM_032536.4:c.565A>G, NM_032536.3:c.565A>G, NM_032536.2:c.565A>G, XM_011519094.3:c.565A>G, XM_011519094.2:c.565A>G, XM_011519094.1:c.565A>G, XM_011519098.3:c.565A>G, XM_011519098.2:c.565A>G, XM_011519098.1:c.565A>G, XM_011519106.3:c.565A>G, XM_011519106.2:c.565A>G, XM_011519106.1:c.565A>G, XM_011519102.3:c.565A>G, XM_011519102.2:c.565A>G, XM_011519102.1:c.565A>G, XM_011519099.3:c.565A>G, XM_011519099.2:c.565A>G, XM_011519099.1:c.565A>G, XM_011519096.3:c.565A>G, XM_011519096.2:c.565A>G, XM_011519096.1:c.565A>G, XM_011519100.3:c.565A>G, XM_011519100.2:c.565A>G, XM_011519100.1:c.565A>G, XM_011519105.3:c.565A>G, XM_011519105.2:c.565A>G, XM_011519105.1:c.565A>G, XM_011519107.3:c.565A>G, XM_011519107.2:c.565A>G, XM_011519107.1:c.565A>G, XM_011519103.3:c.565A>G, XM_011519103.2:c.565A>G, XM_011519103.1:c.565A>G, XM_011519108.3:c.565A>G, XM_011519108.2:c.565A>G, XM_011519108.1:c.565A>G, XM_011519109.3:c.565A>G, XM_011519109.2:c.565A>G, XM_011519109.1:c.565A>G, XM_011519110.3:c.565A>G, XM_011519110.2:c.565A>G, XM_011519110.1:c.565A>G, XM_017015212.2:c.565A>G, XM_017015212.1:c.565A>G, XM_017015213.2:c.565A>G, XM_017015213.1:c.565A>G, XM_017015216.2:c.565A>G, XM_017015216.1:c.565A>G, XM_047423971.1:c.565A>G, XM_047423970.1:c.565A>G, XP_011517399.1:p.Ser189Gly, XP_006717367.1:p.Ser189Gly, XP_011517406.1:p.Ser189Gly, NP_115925.2:p.Ser189Gly, XP_011517396.1:p.Ser189Gly, XP_011517400.1:p.Ser189Gly, XP_011517408.1:p.Ser189Gly, XP_011517404.1:p.Ser189Gly, XP_011517401.1:p.Ser189Gly, XP_011517398.1:p.Ser189Gly, XP_011517402.1:p.Ser189Gly, XP_011517407.1:p.Ser189Gly, XP_011517409.1:p.Ser189Gly, XP_011517405.1:p.Ser189Gly, XP_011517410.1:p.Ser189Gly, XP_011517411.1:p.Ser189Gly, XP_011517412.1:p.Ser189Gly, XP_016870701.1:p.Ser189Gly, XP_016870702.1:p.Ser189Gly, XP_016870705.1:p.Ser189Gly, XP_047279927.1:p.Ser189Gly, XP_047279926.1:p.Ser189Gly

            6.

            rs1472146354 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>A,G [Show Flanks]
              Chromosome:
              9:132167024 (GRCh38)
              9:135042411 (GRCh37)
              Canonical SPDI:
              NC_000009.12:132167023:C:A,NC_000009.12:132167023:C:G
              Gene:
              NTNG2 (Varview)
              Functional Consequence:
              coding_sequence_variant,genic_upstream_transcript_variant,missense_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              G=0./0 (ALFA)
              G=0.000004/1 (TOPMED)
              A=0.000071/2 (TOMMO)
              HGVS:
              NC_000009.12:g.132167024C>A, NC_000009.12:g.132167024C>G, NC_000009.11:g.135042411C>A, NC_000009.11:g.135042411C>G, XM_011519097.4:c.193C>A, XM_011519097.4:c.193C>G, XM_011519097.3:c.193C>A, XM_011519097.3:c.193C>G, XM_011519097.2:c.193C>A, XM_011519097.2:c.193C>G, XM_011519097.1:c.193C>A, XM_011519097.1:c.193C>G, XM_006717304.4:c.193C>A, XM_006717304.4:c.193C>G, XM_006717304.3:c.193C>A, XM_006717304.3:c.193C>G, XM_006717304.2:c.193C>A, XM_006717304.2:c.193C>G, XM_006717304.1:c.193C>A, XM_006717304.1:c.193C>G, XM_011519104.4:c.193C>A, XM_011519104.4:c.193C>G, XM_011519104.3:c.193C>A, XM_011519104.3:c.193C>G, XM_011519104.2:c.193C>A, XM_011519104.2:c.193C>G, XM_011519104.1:c.193C>A, XM_011519104.1:c.193C>G, NM_032536.4:c.193C>A, NM_032536.4:c.193C>G, NM_032536.3:c.193C>A, NM_032536.3:c.193C>G, NM_032536.2:c.193C>A, NM_032536.2:c.193C>G, XM_011519094.3:c.193C>A, XM_011519094.3:c.193C>G, XM_011519094.2:c.193C>A, XM_011519094.2:c.193C>G, XM_011519094.1:c.193C>A, XM_011519094.1:c.193C>G, XM_011519098.3:c.193C>A, XM_011519098.3:c.193C>G, XM_011519098.2:c.193C>A, XM_011519098.2:c.193C>G, XM_011519098.1:c.193C>A, XM_011519098.1:c.193C>G, XM_011519106.3:c.193C>A, XM_011519106.3:c.193C>G, XM_011519106.2:c.193C>A, XM_011519106.2:c.193C>G, XM_011519106.1:c.193C>A, XM_011519106.1:c.193C>G, XM_011519102.3:c.193C>A, XM_011519102.3:c.193C>G, XM_011519102.2:c.193C>A, XM_011519102.2:c.193C>G, XM_011519102.1:c.193C>A, XM_011519102.1:c.193C>G, XM_011519099.3:c.193C>A, XM_011519099.3:c.193C>G, XM_011519099.2:c.193C>A, XM_011519099.2:c.193C>G, XM_011519099.1:c.193C>A, XM_011519099.1:c.193C>G, XM_011519096.3:c.193C>A, XM_011519096.3:c.193C>G, XM_011519096.2:c.193C>A, XM_011519096.2:c.193C>G, XM_011519096.1:c.193C>A, XM_011519096.1:c.193C>G, XM_011519100.3:c.193C>A, XM_011519100.3:c.193C>G, XM_011519100.2:c.193C>A, XM_011519100.2:c.193C>G, XM_011519100.1:c.193C>A, XM_011519100.1:c.193C>G, XM_011519105.3:c.193C>A, XM_011519105.3:c.193C>G, XM_011519105.2:c.193C>A, XM_011519105.2:c.193C>G, XM_011519105.1:c.193C>A, XM_011519105.1:c.193C>G, XM_011519107.3:c.193C>A, XM_011519107.3:c.193C>G, XM_011519107.2:c.193C>A, XM_011519107.2:c.193C>G, XM_011519107.1:c.193C>A, XM_011519107.1:c.193C>G, XM_011519103.3:c.193C>A, XM_011519103.3:c.193C>G, XM_011519103.2:c.193C>A, XM_011519103.2:c.193C>G, XM_011519103.1:c.193C>A, XM_011519103.1:c.193C>G, XM_011519108.3:c.193C>A, XM_011519108.3:c.193C>G, XM_011519108.2:c.193C>A, XM_011519108.2:c.193C>G, XM_011519108.1:c.193C>A, XM_011519108.1:c.193C>G, XM_011519109.3:c.193C>A, XM_011519109.3:c.193C>G, XM_011519109.2:c.193C>A, XM_011519109.2:c.193C>G, XM_011519109.1:c.193C>A, XM_011519109.1:c.193C>G, XM_011519110.3:c.193C>A, XM_011519110.3:c.193C>G, XM_011519110.2:c.193C>A, XM_011519110.2:c.193C>G, XM_011519110.1:c.193C>A, XM_011519110.1:c.193C>G, XM_017015212.2:c.193C>A, XM_017015212.2:c.193C>G, XM_017015212.1:c.193C>A, XM_017015212.1:c.193C>G, XM_017015213.2:c.193C>A, XM_017015213.2:c.193C>G, XM_017015213.1:c.193C>A, XM_017015213.1:c.193C>G, XM_017015216.2:c.193C>A, XM_017015216.2:c.193C>G, XM_017015216.1:c.193C>A, XM_017015216.1:c.193C>G, XM_047423971.1:c.193C>A, XM_047423971.1:c.193C>G, XM_047423970.1:c.193C>A, XM_047423970.1:c.193C>G, XP_011517399.1:p.Pro65Thr, XP_011517399.1:p.Pro65Ala, XP_006717367.1:p.Pro65Thr, XP_006717367.1:p.Pro65Ala, XP_011517406.1:p.Pro65Thr, XP_011517406.1:p.Pro65Ala, NP_115925.2:p.Pro65Thr, NP_115925.2:p.Pro65Ala, XP_011517396.1:p.Pro65Thr, XP_011517396.1:p.Pro65Ala, XP_011517400.1:p.Pro65Thr, XP_011517400.1:p.Pro65Ala, XP_011517408.1:p.Pro65Thr, XP_011517408.1:p.Pro65Ala, XP_011517404.1:p.Pro65Thr, XP_011517404.1:p.Pro65Ala, XP_011517401.1:p.Pro65Thr, XP_011517401.1:p.Pro65Ala, XP_011517398.1:p.Pro65Thr, XP_011517398.1:p.Pro65Ala, XP_011517402.1:p.Pro65Thr, XP_011517402.1:p.Pro65Ala, XP_011517407.1:p.Pro65Thr, XP_011517407.1:p.Pro65Ala, XP_011517409.1:p.Pro65Thr, XP_011517409.1:p.Pro65Ala, XP_011517405.1:p.Pro65Thr, XP_011517405.1:p.Pro65Ala, XP_011517410.1:p.Pro65Thr, XP_011517410.1:p.Pro65Ala, XP_011517411.1:p.Pro65Thr, XP_011517411.1:p.Pro65Ala, XP_011517412.1:p.Pro65Thr, XP_011517412.1:p.Pro65Ala, XP_016870701.1:p.Pro65Thr, XP_016870701.1:p.Pro65Ala, XP_016870702.1:p.Pro65Thr, XP_016870702.1:p.Pro65Ala, XP_016870705.1:p.Pro65Thr, XP_016870705.1:p.Pro65Ala, XP_047279927.1:p.Pro65Thr, XP_047279927.1:p.Pro65Ala, XP_047279926.1:p.Pro65Thr, XP_047279926.1:p.Pro65Ala

              7.

              rs1470528975 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>G [Show Flanks]
                Chromosome:
                9:132198282 (GRCh38)
                9:135073669 (GRCh37)
                Canonical SPDI:
                NC_000009.12:132198281:T:G
                Gene:
                NTNG2 (Varview)
                Functional Consequence:
                coding_sequence_variant,genic_upstream_transcript_variant,missense_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                G=0./0 (ALFA)
                G=0.000004/1 (TOPMED)
                G=0.000007/1 (GnomAD)
                HGVS:
                NC_000009.12:g.132198282T>G, NC_000009.11:g.135073669T>G, XM_011519097.4:c.530T>G, XM_011519097.3:c.530T>G, XM_011519097.2:c.530T>G, XM_011519097.1:c.530T>G, XM_006717304.4:c.530T>G, XM_006717304.3:c.530T>G, XM_006717304.2:c.530T>G, XM_006717304.1:c.530T>G, XM_011519104.4:c.530T>G, XM_011519104.3:c.530T>G, XM_011519104.2:c.530T>G, XM_011519104.1:c.530T>G, NM_032536.4:c.530T>G, NM_032536.3:c.530T>G, NM_032536.2:c.530T>G, XM_011519094.3:c.530T>G, XM_011519094.2:c.530T>G, XM_011519094.1:c.530T>G, XM_011519098.3:c.530T>G, XM_011519098.2:c.530T>G, XM_011519098.1:c.530T>G, XM_011519106.3:c.530T>G, XM_011519106.2:c.530T>G, XM_011519106.1:c.530T>G, XM_011519102.3:c.530T>G, XM_011519102.2:c.530T>G, XM_011519102.1:c.530T>G, XM_011519099.3:c.530T>G, XM_011519099.2:c.530T>G, XM_011519099.1:c.530T>G, XM_011519096.3:c.530T>G, XM_011519096.2:c.530T>G, XM_011519096.1:c.530T>G, XM_011519100.3:c.530T>G, XM_011519100.2:c.530T>G, XM_011519100.1:c.530T>G, XM_011519105.3:c.530T>G, XM_011519105.2:c.530T>G, XM_011519105.1:c.530T>G, XM_011519107.3:c.530T>G, XM_011519107.2:c.530T>G, XM_011519107.1:c.530T>G, XM_011519103.3:c.530T>G, XM_011519103.2:c.530T>G, XM_011519103.1:c.530T>G, XM_011519108.3:c.530T>G, XM_011519108.2:c.530T>G, XM_011519108.1:c.530T>G, XM_011519109.3:c.530T>G, XM_011519109.2:c.530T>G, XM_011519109.1:c.530T>G, XM_011519110.3:c.530T>G, XM_011519110.2:c.530T>G, XM_011519110.1:c.530T>G, XM_017015212.2:c.530T>G, XM_017015212.1:c.530T>G, XM_017015213.2:c.530T>G, XM_017015213.1:c.530T>G, XM_017015216.2:c.530T>G, XM_017015216.1:c.530T>G, XM_047423971.1:c.530T>G, XM_047423970.1:c.530T>G, XP_011517399.1:p.Met177Arg, XP_006717367.1:p.Met177Arg, XP_011517406.1:p.Met177Arg, NP_115925.2:p.Met177Arg, XP_011517396.1:p.Met177Arg, XP_011517400.1:p.Met177Arg, XP_011517408.1:p.Met177Arg, XP_011517404.1:p.Met177Arg, XP_011517401.1:p.Met177Arg, XP_011517398.1:p.Met177Arg, XP_011517402.1:p.Met177Arg, XP_011517407.1:p.Met177Arg, XP_011517409.1:p.Met177Arg, XP_011517405.1:p.Met177Arg, XP_011517410.1:p.Met177Arg, XP_011517411.1:p.Met177Arg, XP_011517412.1:p.Met177Arg, XP_016870701.1:p.Met177Arg, XP_016870702.1:p.Met177Arg, XP_016870705.1:p.Met177Arg, XP_047279927.1:p.Met177Arg, XP_047279926.1:p.Met177Arg

                8.

                rs1467949620 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>A [Show Flanks]
                  Chromosome:
                  9:132198425 (GRCh38)
                  9:135073812 (GRCh37)
                  Canonical SPDI:
                  NC_000009.12:132198424:C:A
                  Gene:
                  NTNG2 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,genic_upstream_transcript_variant,missense_variant
                  HGVS:
                  NC_000009.12:g.132198425C>A, NC_000009.11:g.135073812C>A, XM_011519097.4:c.673C>A, XM_011519097.3:c.673C>A, XM_011519097.2:c.673C>A, XM_011519097.1:c.673C>A, XM_006717304.4:c.673C>A, XM_006717304.3:c.673C>A, XM_006717304.2:c.673C>A, XM_006717304.1:c.673C>A, XM_011519104.4:c.673C>A, XM_011519104.3:c.673C>A, XM_011519104.2:c.673C>A, XM_011519104.1:c.673C>A, NM_032536.4:c.673C>A, NM_032536.3:c.673C>A, NM_032536.2:c.673C>A, XM_011519094.3:c.673C>A, XM_011519094.2:c.673C>A, XM_011519094.1:c.673C>A, XM_011519098.3:c.673C>A, XM_011519098.2:c.673C>A, XM_011519098.1:c.673C>A, XM_011519106.3:c.673C>A, XM_011519106.2:c.673C>A, XM_011519106.1:c.673C>A, XM_011519102.3:c.673C>A, XM_011519102.2:c.673C>A, XM_011519102.1:c.673C>A, XM_011519099.3:c.673C>A, XM_011519099.2:c.673C>A, XM_011519099.1:c.673C>A, XM_011519096.3:c.673C>A, XM_011519096.2:c.673C>A, XM_011519096.1:c.673C>A, XM_011519100.3:c.673C>A, XM_011519100.2:c.673C>A, XM_011519100.1:c.673C>A, XM_011519105.3:c.673C>A, XM_011519105.2:c.673C>A, XM_011519105.1:c.673C>A, XM_011519107.3:c.673C>A, XM_011519107.2:c.673C>A, XM_011519107.1:c.673C>A, XM_011519103.3:c.673C>A, XM_011519103.2:c.673C>A, XM_011519103.1:c.673C>A, XM_011519108.3:c.673C>A, XM_011519108.2:c.673C>A, XM_011519108.1:c.673C>A, XM_011519109.3:c.673C>A, XM_011519109.2:c.673C>A, XM_011519109.1:c.673C>A, XM_011519110.3:c.673C>A, XM_011519110.2:c.673C>A, XM_011519110.1:c.673C>A, XM_017015212.2:c.673C>A, XM_017015212.1:c.673C>A, XM_017015213.2:c.673C>A, XM_017015213.1:c.673C>A, XM_017015216.2:c.673C>A, XM_017015216.1:c.673C>A, XM_047423971.1:c.673C>A, XM_047423970.1:c.673C>A, XP_011517399.1:p.Pro225Thr, XP_006717367.1:p.Pro225Thr, XP_011517406.1:p.Pro225Thr, NP_115925.2:p.Pro225Thr, XP_011517396.1:p.Pro225Thr, XP_011517400.1:p.Pro225Thr, XP_011517408.1:p.Pro225Thr, XP_011517404.1:p.Pro225Thr, XP_011517401.1:p.Pro225Thr, XP_011517398.1:p.Pro225Thr, XP_011517402.1:p.Pro225Thr, XP_011517407.1:p.Pro225Thr, XP_011517409.1:p.Pro225Thr, XP_011517405.1:p.Pro225Thr, XP_011517410.1:p.Pro225Thr, XP_011517411.1:p.Pro225Thr, XP_011517412.1:p.Pro225Thr, XP_016870701.1:p.Pro225Thr, XP_016870702.1:p.Pro225Thr, XP_016870705.1:p.Pro225Thr, XP_047279927.1:p.Pro225Thr, XP_047279926.1:p.Pro225Thr

                  9.

                  rs1463801214 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A [Show Flanks]
                    Chromosome:
                    9:132237244 (GRCh38)
                    9:135112631 (GRCh37)
                    Canonical SPDI:
                    NC_000009.12:132237243:G:A
                    Gene:
                    NTNG2 (Varview)
                    Functional Consequence:
                    coding_sequence_variant,synonymous_variant,intron_variant,genic_downstream_transcript_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    A=0.000054/1 (ALFA)
                    A=0.000023/6 (TOPMED)
                    A=0.000035/1 (TOMMO)
                    A=0.000043/6 (GnomAD)
                    A=0.000223/1 (Estonian)
                    HGVS:

                    10.

                    rs1461146376 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      A>G [Show Flanks]
                      Chromosome:
                      9:132198219 (GRCh38)
                      9:135073606 (GRCh37)
                      Canonical SPDI:
                      NC_000009.12:132198218:A:G
                      Gene:
                      NTNG2 (Varview)
                      Functional Consequence:
                      coding_sequence_variant,missense_variant,genic_upstream_transcript_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      G=0.000047/1 (ALFA)
                      G=0.000004/1 (GnomAD_exomes)
                      HGVS:
                      NC_000009.12:g.132198219A>G, NC_000009.11:g.135073606A>G, XM_011519097.4:c.467A>G, XM_011519097.3:c.467A>G, XM_011519097.2:c.467A>G, XM_011519097.1:c.467A>G, XM_006717304.4:c.467A>G, XM_006717304.3:c.467A>G, XM_006717304.2:c.467A>G, XM_006717304.1:c.467A>G, XM_011519104.4:c.467A>G, XM_011519104.3:c.467A>G, XM_011519104.2:c.467A>G, XM_011519104.1:c.467A>G, NM_032536.4:c.467A>G, NM_032536.3:c.467A>G, NM_032536.2:c.467A>G, XM_011519094.3:c.467A>G, XM_011519094.2:c.467A>G, XM_011519094.1:c.467A>G, XM_011519098.3:c.467A>G, XM_011519098.2:c.467A>G, XM_011519098.1:c.467A>G, XM_011519106.3:c.467A>G, XM_011519106.2:c.467A>G, XM_011519106.1:c.467A>G, XM_011519102.3:c.467A>G, XM_011519102.2:c.467A>G, XM_011519102.1:c.467A>G, XM_011519099.3:c.467A>G, XM_011519099.2:c.467A>G, XM_011519099.1:c.467A>G, XM_011519096.3:c.467A>G, XM_011519096.2:c.467A>G, XM_011519096.1:c.467A>G, XM_011519100.3:c.467A>G, XM_011519100.2:c.467A>G, XM_011519100.1:c.467A>G, XM_011519105.3:c.467A>G, XM_011519105.2:c.467A>G, XM_011519105.1:c.467A>G, XM_011519107.3:c.467A>G, XM_011519107.2:c.467A>G, XM_011519107.1:c.467A>G, XM_011519103.3:c.467A>G, XM_011519103.2:c.467A>G, XM_011519103.1:c.467A>G, XM_011519108.3:c.467A>G, XM_011519108.2:c.467A>G, XM_011519108.1:c.467A>G, XM_011519109.3:c.467A>G, XM_011519109.2:c.467A>G, XM_011519109.1:c.467A>G, XM_011519110.3:c.467A>G, XM_011519110.2:c.467A>G, XM_011519110.1:c.467A>G, XM_017015212.2:c.467A>G, XM_017015212.1:c.467A>G, XM_017015213.2:c.467A>G, XM_017015213.1:c.467A>G, XM_017015216.2:c.467A>G, XM_017015216.1:c.467A>G, XM_047423971.1:c.467A>G, XM_047423970.1:c.467A>G, XP_011517399.1:p.Asp156Gly, XP_006717367.1:p.Asp156Gly, XP_011517406.1:p.Asp156Gly, NP_115925.2:p.Asp156Gly, XP_011517396.1:p.Asp156Gly, XP_011517400.1:p.Asp156Gly, XP_011517408.1:p.Asp156Gly, XP_011517404.1:p.Asp156Gly, XP_011517401.1:p.Asp156Gly, XP_011517398.1:p.Asp156Gly, XP_011517402.1:p.Asp156Gly, XP_011517407.1:p.Asp156Gly, XP_011517409.1:p.Asp156Gly, XP_011517405.1:p.Asp156Gly, XP_011517410.1:p.Asp156Gly, XP_011517411.1:p.Asp156Gly, XP_011517412.1:p.Asp156Gly, XP_016870701.1:p.Asp156Gly, XP_016870702.1:p.Asp156Gly, XP_016870705.1:p.Asp156Gly, XP_047279927.1:p.Asp156Gly, XP_047279926.1:p.Asp156Gly

                      11.

                      rs1460286915 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        CC>- [Show Flanks]
                        Chromosome:
                        9:132231667 (GRCh38)
                        9:135107054 (GRCh37)
                        Canonical SPDI:
                        NC_000009.12:132231664:CCCC:CC
                        Gene:
                        NTNG2 (Varview)
                        Functional Consequence:
                        intron_variant,frameshift_variant,genic_downstream_transcript_variant,coding_sequence_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        CCCC=0./0 (ALFA)
                        -=0.000004/1 (TOPMED)
                        HGVS:
                        NC_000009.12:g.132231667_132231668del, NC_000009.11:g.135107054_135107055del, XM_011519097.4:c.1079_1080del, XM_011519097.3:c.1079_1080del, XM_011519097.2:c.1079_1080del, XM_011519097.1:c.1079_1080del, XM_011519104.4:c.1079_1080del, XM_011519104.3:c.1079_1080del, XM_011519104.2:c.1079_1080del, XM_011519104.1:c.1079_1080del, XM_011519094.3:c.1079_1080del, XM_011519094.2:c.1079_1080del, XM_011519094.1:c.1079_1080del, XM_011519098.3:c.1079_1080del, XM_011519098.2:c.1079_1080del, XM_011519098.1:c.1079_1080del, XM_011519106.3:c.1079_1080del, XM_011519106.2:c.1079_1080del, XM_011519106.1:c.1079_1080del, XM_011519102.3:c.1079_1080del, XM_011519102.2:c.1079_1080del, XM_011519102.1:c.1079_1080del, XM_011519099.3:c.1079_1080del, XM_011519099.2:c.1079_1080del, XM_011519099.1:c.1079_1080del, XM_011519096.3:c.1079_1080del, XM_011519096.2:c.1079_1080del, XM_011519096.1:c.1079_1080del, XM_011519100.3:c.1079_1080del, XM_011519100.2:c.1079_1080del, XM_011519100.1:c.1079_1080del, XM_011519105.3:c.1079_1080del, XM_011519105.2:c.1079_1080del, XM_011519105.1:c.1079_1080del, XM_011519103.3:c.1079_1080del, XM_011519103.2:c.1079_1080del, XM_011519103.1:c.1079_1080del, XM_011519108.3:c.1079_1080del, XM_011519108.2:c.1079_1080del, XM_011519108.1:c.1079_1080del, XM_011519109.3:c.1079_1080del, XM_011519109.2:c.1079_1080del, XM_011519109.1:c.1079_1080del, XM_017015212.2:c.1079_1080del, XM_017015212.1:c.1079_1080del, XM_017015213.2:c.1079_1080del, XM_017015213.1:c.1079_1080del, XM_047423971.1:c.1079_1080del, XM_047423970.1:c.1079_1080del, XP_011517399.1:p.Pro360fs, XP_011517406.1:p.Pro360fs, XP_011517396.1:p.Pro360fs, XP_011517400.1:p.Pro360fs, XP_011517408.1:p.Pro360fs, XP_011517404.1:p.Pro360fs, XP_011517401.1:p.Pro360fs, XP_011517398.1:p.Pro360fs, XP_011517402.1:p.Pro360fs, XP_011517407.1:p.Pro360fs, XP_011517405.1:p.Pro360fs, XP_011517410.1:p.Pro360fs, XP_011517411.1:p.Pro360fs, XP_016870701.1:p.Pro360fs, XP_016870702.1:p.Pro360fs, XP_047279927.1:p.Pro360fs, XP_047279926.1:p.Pro360fs

                        12.

                        rs1458986114 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>A [Show Flanks]
                          Chromosome:
                          9:132198141 (GRCh38)
                          9:135073528 (GRCh37)
                          Canonical SPDI:
                          NC_000009.12:132198140:C:A
                          Gene:
                          NTNG2 (Varview)
                          Functional Consequence:
                          coding_sequence_variant,missense_variant,genic_upstream_transcript_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          A=0.0001/1 (ALFA)
                          HGVS:
                          NC_000009.12:g.132198141C>A, NC_000009.11:g.135073528C>A, XM_011519097.4:c.389C>A, XM_011519097.3:c.389C>A, XM_011519097.2:c.389C>A, XM_011519097.1:c.389C>A, XM_006717304.4:c.389C>A, XM_006717304.3:c.389C>A, XM_006717304.2:c.389C>A, XM_006717304.1:c.389C>A, XM_011519104.4:c.389C>A, XM_011519104.3:c.389C>A, XM_011519104.2:c.389C>A, XM_011519104.1:c.389C>A, NM_032536.4:c.389C>A, NM_032536.3:c.389C>A, NM_032536.2:c.389C>A, XM_011519094.3:c.389C>A, XM_011519094.2:c.389C>A, XM_011519094.1:c.389C>A, XM_011519098.3:c.389C>A, XM_011519098.2:c.389C>A, XM_011519098.1:c.389C>A, XM_011519106.3:c.389C>A, XM_011519106.2:c.389C>A, XM_011519106.1:c.389C>A, XM_011519102.3:c.389C>A, XM_011519102.2:c.389C>A, XM_011519102.1:c.389C>A, XM_011519099.3:c.389C>A, XM_011519099.2:c.389C>A, XM_011519099.1:c.389C>A, XM_011519096.3:c.389C>A, XM_011519096.2:c.389C>A, XM_011519096.1:c.389C>A, XM_011519100.3:c.389C>A, XM_011519100.2:c.389C>A, XM_011519100.1:c.389C>A, XM_011519105.3:c.389C>A, XM_011519105.2:c.389C>A, XM_011519105.1:c.389C>A, XM_011519107.3:c.389C>A, XM_011519107.2:c.389C>A, XM_011519107.1:c.389C>A, XM_011519103.3:c.389C>A, XM_011519103.2:c.389C>A, XM_011519103.1:c.389C>A, XM_011519108.3:c.389C>A, XM_011519108.2:c.389C>A, XM_011519108.1:c.389C>A, XM_011519109.3:c.389C>A, XM_011519109.2:c.389C>A, XM_011519109.1:c.389C>A, XM_011519110.3:c.389C>A, XM_011519110.2:c.389C>A, XM_011519110.1:c.389C>A, XM_017015212.2:c.389C>A, XM_017015212.1:c.389C>A, XM_017015213.2:c.389C>A, XM_017015213.1:c.389C>A, XM_017015216.2:c.389C>A, XM_017015216.1:c.389C>A, XM_047423971.1:c.389C>A, XM_047423970.1:c.389C>A, XP_011517399.1:p.Thr130Asn, XP_006717367.1:p.Thr130Asn, XP_011517406.1:p.Thr130Asn, NP_115925.2:p.Thr130Asn, XP_011517396.1:p.Thr130Asn, XP_011517400.1:p.Thr130Asn, XP_011517408.1:p.Thr130Asn, XP_011517404.1:p.Thr130Asn, XP_011517401.1:p.Thr130Asn, XP_011517398.1:p.Thr130Asn, XP_011517402.1:p.Thr130Asn, XP_011517407.1:p.Thr130Asn, XP_011517409.1:p.Thr130Asn, XP_011517405.1:p.Thr130Asn, XP_011517410.1:p.Thr130Asn, XP_011517411.1:p.Thr130Asn, XP_011517412.1:p.Thr130Asn, XP_016870701.1:p.Thr130Asn, XP_016870702.1:p.Thr130Asn, XP_016870705.1:p.Thr130Asn, XP_047279927.1:p.Thr130Asn, XP_047279926.1:p.Thr130Asn

                          13.

                          rs1442339467 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            A>G [Show Flanks]
                            Chromosome:
                            9:132198138 (GRCh38)
                            9:135073525 (GRCh37)
                            Canonical SPDI:
                            NC_000009.12:132198137:A:G
                            Gene:
                            NTNG2 (Varview)
                            Functional Consequence:
                            missense_variant,coding_sequence_variant,genic_upstream_transcript_variant
                            Validated:
                            by frequency
                            MAF:
                            G=0.000004/1 (GnomAD_exomes)
                            HGVS:
                            NC_000009.12:g.132198138A>G, NC_000009.11:g.135073525A>G, XM_011519097.4:c.386A>G, XM_011519097.3:c.386A>G, XM_011519097.2:c.386A>G, XM_011519097.1:c.386A>G, XM_006717304.4:c.386A>G, XM_006717304.3:c.386A>G, XM_006717304.2:c.386A>G, XM_006717304.1:c.386A>G, XM_011519104.4:c.386A>G, XM_011519104.3:c.386A>G, XM_011519104.2:c.386A>G, XM_011519104.1:c.386A>G, NM_032536.4:c.386A>G, NM_032536.3:c.386A>G, NM_032536.2:c.386A>G, XM_011519094.3:c.386A>G, XM_011519094.2:c.386A>G, XM_011519094.1:c.386A>G, XM_011519098.3:c.386A>G, XM_011519098.2:c.386A>G, XM_011519098.1:c.386A>G, XM_011519106.3:c.386A>G, XM_011519106.2:c.386A>G, XM_011519106.1:c.386A>G, XM_011519102.3:c.386A>G, XM_011519102.2:c.386A>G, XM_011519102.1:c.386A>G, XM_011519099.3:c.386A>G, XM_011519099.2:c.386A>G, XM_011519099.1:c.386A>G, XM_011519096.3:c.386A>G, XM_011519096.2:c.386A>G, XM_011519096.1:c.386A>G, XM_011519100.3:c.386A>G, XM_011519100.2:c.386A>G, XM_011519100.1:c.386A>G, XM_011519105.3:c.386A>G, XM_011519105.2:c.386A>G, XM_011519105.1:c.386A>G, XM_011519107.3:c.386A>G, XM_011519107.2:c.386A>G, XM_011519107.1:c.386A>G, XM_011519103.3:c.386A>G, XM_011519103.2:c.386A>G, XM_011519103.1:c.386A>G, XM_011519108.3:c.386A>G, XM_011519108.2:c.386A>G, XM_011519108.1:c.386A>G, XM_011519109.3:c.386A>G, XM_011519109.2:c.386A>G, XM_011519109.1:c.386A>G, XM_011519110.3:c.386A>G, XM_011519110.2:c.386A>G, XM_011519110.1:c.386A>G, XM_017015212.2:c.386A>G, XM_017015212.1:c.386A>G, XM_017015213.2:c.386A>G, XM_017015213.1:c.386A>G, XM_017015216.2:c.386A>G, XM_017015216.1:c.386A>G, XM_047423971.1:c.386A>G, XM_047423970.1:c.386A>G, XP_011517399.1:p.Lys129Arg, XP_006717367.1:p.Lys129Arg, XP_011517406.1:p.Lys129Arg, NP_115925.2:p.Lys129Arg, XP_011517396.1:p.Lys129Arg, XP_011517400.1:p.Lys129Arg, XP_011517408.1:p.Lys129Arg, XP_011517404.1:p.Lys129Arg, XP_011517401.1:p.Lys129Arg, XP_011517398.1:p.Lys129Arg, XP_011517402.1:p.Lys129Arg, XP_011517407.1:p.Lys129Arg, XP_011517409.1:p.Lys129Arg, XP_011517405.1:p.Lys129Arg, XP_011517410.1:p.Lys129Arg, XP_011517411.1:p.Lys129Arg, XP_011517412.1:p.Lys129Arg, XP_016870701.1:p.Lys129Arg, XP_016870702.1:p.Lys129Arg, XP_016870705.1:p.Lys129Arg, XP_047279927.1:p.Lys129Arg, XP_047279926.1:p.Lys129Arg

                            14.

                            rs1440293405 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A [Show Flanks]
                              Chromosome:
                              9:132198062 (GRCh38)
                              9:135073449 (GRCh37)
                              Canonical SPDI:
                              NC_000009.12:132198061:G:A
                              Gene:
                              NTNG2 (Varview)
                              Functional Consequence:
                              missense_variant,coding_sequence_variant,genic_upstream_transcript_variant
                              Validated:
                              by frequency,by cluster
                              MAF:
                              A=0.000007/1 (GnomAD)
                              HGVS:
                              NC_000009.12:g.132198062G>A, NC_000009.11:g.135073449G>A, XM_011519097.4:c.310G>A, XM_011519097.3:c.310G>A, XM_011519097.2:c.310G>A, XM_011519097.1:c.310G>A, XM_006717304.4:c.310G>A, XM_006717304.3:c.310G>A, XM_006717304.2:c.310G>A, XM_006717304.1:c.310G>A, XM_011519104.4:c.310G>A, XM_011519104.3:c.310G>A, XM_011519104.2:c.310G>A, XM_011519104.1:c.310G>A, NM_032536.4:c.310G>A, NM_032536.3:c.310G>A, NM_032536.2:c.310G>A, XM_011519094.3:c.310G>A, XM_011519094.2:c.310G>A, XM_011519094.1:c.310G>A, XM_011519098.3:c.310G>A, XM_011519098.2:c.310G>A, XM_011519098.1:c.310G>A, XM_011519106.3:c.310G>A, XM_011519106.2:c.310G>A, XM_011519106.1:c.310G>A, XM_011519102.3:c.310G>A, XM_011519102.2:c.310G>A, XM_011519102.1:c.310G>A, XM_011519099.3:c.310G>A, XM_011519099.2:c.310G>A, XM_011519099.1:c.310G>A, XM_011519096.3:c.310G>A, XM_011519096.2:c.310G>A, XM_011519096.1:c.310G>A, XM_011519100.3:c.310G>A, XM_011519100.2:c.310G>A, XM_011519100.1:c.310G>A, XM_011519105.3:c.310G>A, XM_011519105.2:c.310G>A, XM_011519105.1:c.310G>A, XM_011519107.3:c.310G>A, XM_011519107.2:c.310G>A, XM_011519107.1:c.310G>A, XM_011519103.3:c.310G>A, XM_011519103.2:c.310G>A, XM_011519103.1:c.310G>A, XM_011519108.3:c.310G>A, XM_011519108.2:c.310G>A, XM_011519108.1:c.310G>A, XM_011519109.3:c.310G>A, XM_011519109.2:c.310G>A, XM_011519109.1:c.310G>A, XM_011519110.3:c.310G>A, XM_011519110.2:c.310G>A, XM_011519110.1:c.310G>A, XM_017015212.2:c.310G>A, XM_017015212.1:c.310G>A, XM_017015213.2:c.310G>A, XM_017015213.1:c.310G>A, XM_017015216.2:c.310G>A, XM_017015216.1:c.310G>A, XM_047423971.1:c.310G>A, XM_047423970.1:c.310G>A, XP_011517399.1:p.Ala104Thr, XP_006717367.1:p.Ala104Thr, XP_011517406.1:p.Ala104Thr, NP_115925.2:p.Ala104Thr, XP_011517396.1:p.Ala104Thr, XP_011517400.1:p.Ala104Thr, XP_011517408.1:p.Ala104Thr, XP_011517404.1:p.Ala104Thr, XP_011517401.1:p.Ala104Thr, XP_011517398.1:p.Ala104Thr, XP_011517402.1:p.Ala104Thr, XP_011517407.1:p.Ala104Thr, XP_011517409.1:p.Ala104Thr, XP_011517405.1:p.Ala104Thr, XP_011517410.1:p.Ala104Thr, XP_011517411.1:p.Ala104Thr, XP_011517412.1:p.Ala104Thr, XP_016870701.1:p.Ala104Thr, XP_016870702.1:p.Ala104Thr, XP_016870705.1:p.Ala104Thr, XP_047279927.1:p.Ala104Thr, XP_047279926.1:p.Ala104Thr

                              15.

                              rs1439905207 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                9:132231788 (GRCh38)
                                9:135107175 (GRCh37)
                                Canonical SPDI:
                                NC_000009.12:132231787:A:G
                                Gene:
                                NTNG2 (Varview)
                                Functional Consequence:
                                coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant,intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                G=0./0 (ALFA)
                                G=0.000004/1 (TOPMED)
                                HGVS:
                                NC_000009.12:g.132231788A>G, NC_000009.11:g.135107175A>G, XM_011519097.4:c.1200A>G, XM_011519097.3:c.1200A>G, XM_011519097.2:c.1200A>G, XM_011519097.1:c.1200A>G, XM_011519104.4:c.1200A>G, XM_011519104.3:c.1200A>G, XM_011519104.2:c.1200A>G, XM_011519104.1:c.1200A>G, XM_011519094.3:c.1200A>G, XM_011519094.2:c.1200A>G, XM_011519094.1:c.1200A>G, XM_011519098.3:c.1200A>G, XM_011519098.2:c.1200A>G, XM_011519098.1:c.1200A>G, XM_011519106.3:c.1200A>G, XM_011519106.2:c.1200A>G, XM_011519106.1:c.1200A>G, XM_011519102.3:c.1200A>G, XM_011519102.2:c.1200A>G, XM_011519102.1:c.1200A>G, XM_011519099.3:c.1200A>G, XM_011519099.2:c.1200A>G, XM_011519099.1:c.1200A>G, XM_011519096.3:c.1200A>G, XM_011519096.2:c.1200A>G, XM_011519096.1:c.1200A>G, XM_011519100.3:c.1200A>G, XM_011519100.2:c.1200A>G, XM_011519100.1:c.1200A>G, XM_011519105.3:c.1200A>G, XM_011519105.2:c.1200A>G, XM_011519105.1:c.1200A>G, XM_011519103.3:c.1200A>G, XM_011519103.2:c.1200A>G, XM_011519103.1:c.1200A>G, XM_011519108.3:c.1200A>G, XM_011519108.2:c.1200A>G, XM_011519108.1:c.1200A>G, XM_011519109.3:c.1200A>G, XM_011519109.2:c.1200A>G, XM_011519109.1:c.1200A>G, XM_017015212.2:c.1200A>G, XM_017015212.1:c.1200A>G, XM_017015213.2:c.1200A>G, XM_017015213.1:c.1200A>G, XM_047423971.1:c.1200A>G, XM_047423970.1:c.1200A>G

                                16.

                                rs1439226296 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  A>C,T [Show Flanks]
                                  Chromosome:
                                  9:132198101 (GRCh38)
                                  9:135073488 (GRCh37)
                                  Canonical SPDI:
                                  NC_000009.12:132198100:A:C,NC_000009.12:132198100:A:T
                                  Gene:
                                  NTNG2 (Varview)
                                  Functional Consequence:
                                  missense_variant,coding_sequence_variant,genic_upstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  C=0./0 (ALFA)
                                  C=0.000004/1 (TOPMED)
                                  C=0.000007/1 (GnomAD)
                                  T=0.000546/1 (Korea1K)
                                  HGVS:
                                  NC_000009.12:g.132198101A>C, NC_000009.12:g.132198101A>T, NC_000009.11:g.135073488A>C, NC_000009.11:g.135073488A>T, XM_011519097.4:c.349A>C, XM_011519097.4:c.349A>T, XM_011519097.3:c.349A>C, XM_011519097.3:c.349A>T, XM_011519097.2:c.349A>C, XM_011519097.2:c.349A>T, XM_011519097.1:c.349A>C, XM_011519097.1:c.349A>T, XM_006717304.4:c.349A>C, XM_006717304.4:c.349A>T, XM_006717304.3:c.349A>C, XM_006717304.3:c.349A>T, XM_006717304.2:c.349A>C, XM_006717304.2:c.349A>T, XM_006717304.1:c.349A>C, XM_006717304.1:c.349A>T, XM_011519104.4:c.349A>C, XM_011519104.4:c.349A>T, XM_011519104.3:c.349A>C, XM_011519104.3:c.349A>T, XM_011519104.2:c.349A>C, XM_011519104.2:c.349A>T, XM_011519104.1:c.349A>C, XM_011519104.1:c.349A>T, NM_032536.4:c.349A>C, NM_032536.4:c.349A>T, NM_032536.3:c.349A>C, NM_032536.3:c.349A>T, NM_032536.2:c.349A>C, NM_032536.2:c.349A>T, XM_011519094.3:c.349A>C, XM_011519094.3:c.349A>T, XM_011519094.2:c.349A>C, XM_011519094.2:c.349A>T, XM_011519094.1:c.349A>C, XM_011519094.1:c.349A>T, XM_011519098.3:c.349A>C, XM_011519098.3:c.349A>T, XM_011519098.2:c.349A>C, XM_011519098.2:c.349A>T, XM_011519098.1:c.349A>C, XM_011519098.1:c.349A>T, XM_011519106.3:c.349A>C, XM_011519106.3:c.349A>T, XM_011519106.2:c.349A>C, XM_011519106.2:c.349A>T, XM_011519106.1:c.349A>C, XM_011519106.1:c.349A>T, XM_011519102.3:c.349A>C, XM_011519102.3:c.349A>T, XM_011519102.2:c.349A>C, XM_011519102.2:c.349A>T, XM_011519102.1:c.349A>C, XM_011519102.1:c.349A>T, XM_011519099.3:c.349A>C, XM_011519099.3:c.349A>T, XM_011519099.2:c.349A>C, XM_011519099.2:c.349A>T, XM_011519099.1:c.349A>C, XM_011519099.1:c.349A>T, XM_011519096.3:c.349A>C, XM_011519096.3:c.349A>T, XM_011519096.2:c.349A>C, XM_011519096.2:c.349A>T, XM_011519096.1:c.349A>C, XM_011519096.1:c.349A>T, XM_011519100.3:c.349A>C, XM_011519100.3:c.349A>T, XM_011519100.2:c.349A>C, XM_011519100.2:c.349A>T, XM_011519100.1:c.349A>C, XM_011519100.1:c.349A>T, XM_011519105.3:c.349A>C, XM_011519105.3:c.349A>T, XM_011519105.2:c.349A>C, XM_011519105.2:c.349A>T, XM_011519105.1:c.349A>C, XM_011519105.1:c.349A>T, XM_011519107.3:c.349A>C, XM_011519107.3:c.349A>T, XM_011519107.2:c.349A>C, XM_011519107.2:c.349A>T, XM_011519107.1:c.349A>C, XM_011519107.1:c.349A>T, XM_011519103.3:c.349A>C, XM_011519103.3:c.349A>T, XM_011519103.2:c.349A>C, XM_011519103.2:c.349A>T, XM_011519103.1:c.349A>C, XM_011519103.1:c.349A>T, XM_011519108.3:c.349A>C, XM_011519108.3:c.349A>T, XM_011519108.2:c.349A>C, XM_011519108.2:c.349A>T, XM_011519108.1:c.349A>C, XM_011519108.1:c.349A>T, XM_011519109.3:c.349A>C, XM_011519109.3:c.349A>T, XM_011519109.2:c.349A>C, XM_011519109.2:c.349A>T, XM_011519109.1:c.349A>C, XM_011519109.1:c.349A>T, XM_011519110.3:c.349A>C, XM_011519110.3:c.349A>T, XM_011519110.2:c.349A>C, XM_011519110.2:c.349A>T, XM_011519110.1:c.349A>C, XM_011519110.1:c.349A>T, XM_017015212.2:c.349A>C, XM_017015212.2:c.349A>T, XM_017015212.1:c.349A>C, XM_017015212.1:c.349A>T, XM_017015213.2:c.349A>C, XM_017015213.2:c.349A>T, XM_017015213.1:c.349A>C, XM_017015213.1:c.349A>T, XM_017015216.2:c.349A>C, XM_017015216.2:c.349A>T, XM_017015216.1:c.349A>C, XM_017015216.1:c.349A>T, XM_047423971.1:c.349A>C, XM_047423971.1:c.349A>T, XM_047423970.1:c.349A>C, XM_047423970.1:c.349A>T, XP_011517399.1:p.Ser117Arg, XP_011517399.1:p.Ser117Cys, XP_006717367.1:p.Ser117Arg, XP_006717367.1:p.Ser117Cys, XP_011517406.1:p.Ser117Arg, XP_011517406.1:p.Ser117Cys, NP_115925.2:p.Ser117Arg, NP_115925.2:p.Ser117Cys, XP_011517396.1:p.Ser117Arg, XP_011517396.1:p.Ser117Cys, XP_011517400.1:p.Ser117Arg, XP_011517400.1:p.Ser117Cys, XP_011517408.1:p.Ser117Arg, XP_011517408.1:p.Ser117Cys, XP_011517404.1:p.Ser117Arg, XP_011517404.1:p.Ser117Cys, XP_011517401.1:p.Ser117Arg, XP_011517401.1:p.Ser117Cys, XP_011517398.1:p.Ser117Arg, XP_011517398.1:p.Ser117Cys, XP_011517402.1:p.Ser117Arg, XP_011517402.1:p.Ser117Cys, XP_011517407.1:p.Ser117Arg, XP_011517407.1:p.Ser117Cys, XP_011517409.1:p.Ser117Arg, XP_011517409.1:p.Ser117Cys, XP_011517405.1:p.Ser117Arg, XP_011517405.1:p.Ser117Cys, XP_011517410.1:p.Ser117Arg, XP_011517410.1:p.Ser117Cys, XP_011517411.1:p.Ser117Arg, XP_011517411.1:p.Ser117Cys, XP_011517412.1:p.Ser117Arg, XP_011517412.1:p.Ser117Cys, XP_016870701.1:p.Ser117Arg, XP_016870701.1:p.Ser117Cys, XP_016870702.1:p.Ser117Arg, XP_016870702.1:p.Ser117Cys, XP_016870705.1:p.Ser117Arg, XP_016870705.1:p.Ser117Cys, XP_047279927.1:p.Ser117Arg, XP_047279927.1:p.Ser117Cys, XP_047279926.1:p.Ser117Arg, XP_047279926.1:p.Ser117Cys

                                  17.

                                  rs1439066736 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>G [Show Flanks]
                                    Chromosome:
                                    9:132198168 (GRCh38)
                                    9:135073555 (GRCh37)
                                    Canonical SPDI:
                                    NC_000009.12:132198167:T:G
                                    Gene:
                                    NTNG2 (Varview)
                                    Functional Consequence:
                                    missense_variant,coding_sequence_variant,genic_upstream_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0./0 (ALFA)
                                    G=0.000007/1 (GnomAD)
                                    HGVS:
                                    NC_000009.12:g.132198168T>G, NC_000009.11:g.135073555T>G, XM_011519097.4:c.416T>G, XM_011519097.3:c.416T>G, XM_011519097.2:c.416T>G, XM_011519097.1:c.416T>G, XM_006717304.4:c.416T>G, XM_006717304.3:c.416T>G, XM_006717304.2:c.416T>G, XM_006717304.1:c.416T>G, XM_011519104.4:c.416T>G, XM_011519104.3:c.416T>G, XM_011519104.2:c.416T>G, XM_011519104.1:c.416T>G, NM_032536.4:c.416T>G, NM_032536.3:c.416T>G, NM_032536.2:c.416T>G, XM_011519094.3:c.416T>G, XM_011519094.2:c.416T>G, XM_011519094.1:c.416T>G, XM_011519098.3:c.416T>G, XM_011519098.2:c.416T>G, XM_011519098.1:c.416T>G, XM_011519106.3:c.416T>G, XM_011519106.2:c.416T>G, XM_011519106.1:c.416T>G, XM_011519102.3:c.416T>G, XM_011519102.2:c.416T>G, XM_011519102.1:c.416T>G, XM_011519099.3:c.416T>G, XM_011519099.2:c.416T>G, XM_011519099.1:c.416T>G, XM_011519096.3:c.416T>G, XM_011519096.2:c.416T>G, XM_011519096.1:c.416T>G, XM_011519100.3:c.416T>G, XM_011519100.2:c.416T>G, XM_011519100.1:c.416T>G, XM_011519105.3:c.416T>G, XM_011519105.2:c.416T>G, XM_011519105.1:c.416T>G, XM_011519107.3:c.416T>G, XM_011519107.2:c.416T>G, XM_011519107.1:c.416T>G, XM_011519103.3:c.416T>G, XM_011519103.2:c.416T>G, XM_011519103.1:c.416T>G, XM_011519108.3:c.416T>G, XM_011519108.2:c.416T>G, XM_011519108.1:c.416T>G, XM_011519109.3:c.416T>G, XM_011519109.2:c.416T>G, XM_011519109.1:c.416T>G, XM_011519110.3:c.416T>G, XM_011519110.2:c.416T>G, XM_011519110.1:c.416T>G, XM_017015212.2:c.416T>G, XM_017015212.1:c.416T>G, XM_017015213.2:c.416T>G, XM_017015213.1:c.416T>G, XM_017015216.2:c.416T>G, XM_017015216.1:c.416T>G, XM_047423971.1:c.416T>G, XM_047423970.1:c.416T>G, XP_011517399.1:p.Met139Arg, XP_006717367.1:p.Met139Arg, XP_011517406.1:p.Met139Arg, NP_115925.2:p.Met139Arg, XP_011517396.1:p.Met139Arg, XP_011517400.1:p.Met139Arg, XP_011517408.1:p.Met139Arg, XP_011517404.1:p.Met139Arg, XP_011517401.1:p.Met139Arg, XP_011517398.1:p.Met139Arg, XP_011517402.1:p.Met139Arg, XP_011517407.1:p.Met139Arg, XP_011517409.1:p.Met139Arg, XP_011517405.1:p.Met139Arg, XP_011517410.1:p.Met139Arg, XP_011517411.1:p.Met139Arg, XP_011517412.1:p.Met139Arg, XP_016870701.1:p.Met139Arg, XP_016870702.1:p.Met139Arg, XP_016870705.1:p.Met139Arg, XP_047279927.1:p.Met139Arg, XP_047279926.1:p.Met139Arg

                                    18.

                                    rs1437727556 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>A,T [Show Flanks]
                                      Chromosome:
                                      9:132198398 (GRCh38)
                                      9:135073785 (GRCh37)
                                      Canonical SPDI:
                                      NC_000009.12:132198397:C:A,NC_000009.12:132198397:C:T
                                      Gene:
                                      NTNG2 (Varview)
                                      Functional Consequence:
                                      missense_variant,coding_sequence_variant,synonymous_variant,genic_upstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0./0 (ALFA)
                                      A=0.000004/1 (GnomAD_exomes)
                                      T=0.000004/1 (TOPMED)
                                      HGVS:
                                      NC_000009.12:g.132198398C>A, NC_000009.12:g.132198398C>T, NC_000009.11:g.135073785C>A, NC_000009.11:g.135073785C>T, XM_011519097.4:c.646C>A, XM_011519097.4:c.646C>T, XM_011519097.3:c.646C>A, XM_011519097.3:c.646C>T, XM_011519097.2:c.646C>A, XM_011519097.2:c.646C>T, XM_011519097.1:c.646C>A, XM_011519097.1:c.646C>T, XM_006717304.4:c.646C>A, XM_006717304.4:c.646C>T, XM_006717304.3:c.646C>A, XM_006717304.3:c.646C>T, XM_006717304.2:c.646C>A, XM_006717304.2:c.646C>T, XM_006717304.1:c.646C>A, XM_006717304.1:c.646C>T, XM_011519104.4:c.646C>A, XM_011519104.4:c.646C>T, XM_011519104.3:c.646C>A, XM_011519104.3:c.646C>T, XM_011519104.2:c.646C>A, XM_011519104.2:c.646C>T, XM_011519104.1:c.646C>A, XM_011519104.1:c.646C>T, NM_032536.4:c.646C>A, NM_032536.4:c.646C>T, NM_032536.3:c.646C>A, NM_032536.3:c.646C>T, NM_032536.2:c.646C>A, NM_032536.2:c.646C>T, XM_011519094.3:c.646C>A, XM_011519094.3:c.646C>T, XM_011519094.2:c.646C>A, XM_011519094.2:c.646C>T, XM_011519094.1:c.646C>A, XM_011519094.1:c.646C>T, XM_011519098.3:c.646C>A, XM_011519098.3:c.646C>T, XM_011519098.2:c.646C>A, XM_011519098.2:c.646C>T, XM_011519098.1:c.646C>A, XM_011519098.1:c.646C>T, XM_011519106.3:c.646C>A, XM_011519106.3:c.646C>T, XM_011519106.2:c.646C>A, XM_011519106.2:c.646C>T, XM_011519106.1:c.646C>A, XM_011519106.1:c.646C>T, XM_011519102.3:c.646C>A, XM_011519102.3:c.646C>T, XM_011519102.2:c.646C>A, XM_011519102.2:c.646C>T, XM_011519102.1:c.646C>A, XM_011519102.1:c.646C>T, XM_011519099.3:c.646C>A, XM_011519099.3:c.646C>T, XM_011519099.2:c.646C>A, XM_011519099.2:c.646C>T, XM_011519099.1:c.646C>A, XM_011519099.1:c.646C>T, XM_011519096.3:c.646C>A, XM_011519096.3:c.646C>T, XM_011519096.2:c.646C>A, XM_011519096.2:c.646C>T, XM_011519096.1:c.646C>A, XM_011519096.1:c.646C>T, XM_011519100.3:c.646C>A, XM_011519100.3:c.646C>T, XM_011519100.2:c.646C>A, XM_011519100.2:c.646C>T, XM_011519100.1:c.646C>A, XM_011519100.1:c.646C>T, XM_011519105.3:c.646C>A, XM_011519105.3:c.646C>T, XM_011519105.2:c.646C>A, XM_011519105.2:c.646C>T, XM_011519105.1:c.646C>A, XM_011519105.1:c.646C>T, XM_011519107.3:c.646C>A, XM_011519107.3:c.646C>T, XM_011519107.2:c.646C>A, XM_011519107.2:c.646C>T, XM_011519107.1:c.646C>A, XM_011519107.1:c.646C>T, XM_011519103.3:c.646C>A, XM_011519103.3:c.646C>T, XM_011519103.2:c.646C>A, XM_011519103.2:c.646C>T, XM_011519103.1:c.646C>A, XM_011519103.1:c.646C>T, XM_011519108.3:c.646C>A, XM_011519108.3:c.646C>T, XM_011519108.2:c.646C>A, XM_011519108.2:c.646C>T, XM_011519108.1:c.646C>A, XM_011519108.1:c.646C>T, XM_011519109.3:c.646C>A, XM_011519109.3:c.646C>T, XM_011519109.2:c.646C>A, XM_011519109.2:c.646C>T, XM_011519109.1:c.646C>A, XM_011519109.1:c.646C>T, XM_011519110.3:c.646C>A, XM_011519110.3:c.646C>T, XM_011519110.2:c.646C>A, XM_011519110.2:c.646C>T, XM_011519110.1:c.646C>A, XM_011519110.1:c.646C>T, XM_017015212.2:c.646C>A, XM_017015212.2:c.646C>T, XM_017015212.1:c.646C>A, XM_017015212.1:c.646C>T, XM_017015213.2:c.646C>A, XM_017015213.2:c.646C>T, XM_017015213.1:c.646C>A, XM_017015213.1:c.646C>T, XM_017015216.2:c.646C>A, XM_017015216.2:c.646C>T, XM_017015216.1:c.646C>A, XM_017015216.1:c.646C>T, XM_047423971.1:c.646C>A, XM_047423971.1:c.646C>T, XM_047423970.1:c.646C>A, XM_047423970.1:c.646C>T, XP_011517399.1:p.Arg216Trp, XP_006717367.1:p.Arg216Trp, XP_011517406.1:p.Arg216Trp, NP_115925.2:p.Arg216Trp, XP_011517396.1:p.Arg216Trp, XP_011517400.1:p.Arg216Trp, XP_011517408.1:p.Arg216Trp, XP_011517404.1:p.Arg216Trp, XP_011517401.1:p.Arg216Trp, XP_011517398.1:p.Arg216Trp, XP_011517402.1:p.Arg216Trp, XP_011517407.1:p.Arg216Trp, XP_011517409.1:p.Arg216Trp, XP_011517405.1:p.Arg216Trp, XP_011517410.1:p.Arg216Trp, XP_011517411.1:p.Arg216Trp, XP_011517412.1:p.Arg216Trp, XP_016870701.1:p.Arg216Trp, XP_016870702.1:p.Arg216Trp, XP_016870705.1:p.Arg216Trp, XP_047279927.1:p.Arg216Trp, XP_047279926.1:p.Arg216Trp

                                      19.

                                      rs1436740071 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>T [Show Flanks]
                                        Chromosome:
                                        9:132198478 (GRCh38)
                                        9:135073865 (GRCh37)
                                        Canonical SPDI:
                                        NC_000009.12:132198477:C:T
                                        Gene:
                                        NTNG2 (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,synonymous_variant,genic_upstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        T=0./0 (ALFA)
                                        T=0.000004/1 (GnomAD_exomes)
                                        HGVS:
                                        NC_000009.12:g.132198478C>T, NC_000009.11:g.135073865C>T, XM_011519097.4:c.726C>T, XM_011519097.3:c.726C>T, XM_011519097.2:c.726C>T, XM_011519097.1:c.726C>T, XM_006717304.4:c.726C>T, XM_006717304.3:c.726C>T, XM_006717304.2:c.726C>T, XM_006717304.1:c.726C>T, XM_011519104.4:c.726C>T, XM_011519104.3:c.726C>T, XM_011519104.2:c.726C>T, XM_011519104.1:c.726C>T, NM_032536.4:c.726C>T, NM_032536.3:c.726C>T, NM_032536.2:c.726C>T, XM_011519094.3:c.726C>T, XM_011519094.2:c.726C>T, XM_011519094.1:c.726C>T, XM_011519098.3:c.726C>T, XM_011519098.2:c.726C>T, XM_011519098.1:c.726C>T, XM_011519106.3:c.726C>T, XM_011519106.2:c.726C>T, XM_011519106.1:c.726C>T, XM_011519102.3:c.726C>T, XM_011519102.2:c.726C>T, XM_011519102.1:c.726C>T, XM_011519099.3:c.726C>T, XM_011519099.2:c.726C>T, XM_011519099.1:c.726C>T, XM_011519096.3:c.726C>T, XM_011519096.2:c.726C>T, XM_011519096.1:c.726C>T, XM_011519100.3:c.726C>T, XM_011519100.2:c.726C>T, XM_011519100.1:c.726C>T, XM_011519105.3:c.726C>T, XM_011519105.2:c.726C>T, XM_011519105.1:c.726C>T, XM_011519107.3:c.726C>T, XM_011519107.2:c.726C>T, XM_011519107.1:c.726C>T, XM_011519103.3:c.726C>T, XM_011519103.2:c.726C>T, XM_011519103.1:c.726C>T, XM_011519108.3:c.726C>T, XM_011519108.2:c.726C>T, XM_011519108.1:c.726C>T, XM_011519109.3:c.726C>T, XM_011519109.2:c.726C>T, XM_011519109.1:c.726C>T, XM_011519110.3:c.726C>T, XM_011519110.2:c.726C>T, XM_011519110.1:c.726C>T, XM_017015212.2:c.726C>T, XM_017015212.1:c.726C>T, XM_017015213.2:c.726C>T, XM_017015213.1:c.726C>T, XM_017015216.2:c.726C>T, XM_017015216.1:c.726C>T, XM_047423971.1:c.726C>T, XM_047423970.1:c.726C>T

                                        20.

                                        rs1430681418 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>G [Show Flanks]
                                          Chromosome:
                                          9:132198465 (GRCh38)
                                          9:135073852 (GRCh37)
                                          Canonical SPDI:
                                          NC_000009.12:132198464:A:G
                                          Gene:
                                          NTNG2 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,genic_upstream_transcript_variant,missense_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          G=0./0 (ALFA)
                                          G=0.000004/1 (GnomAD_exomes)
                                          G=0.000004/1 (TOPMED)
                                          HGVS:
                                          NC_000009.12:g.132198465A>G, NC_000009.11:g.135073852A>G, XM_011519097.4:c.713A>G, XM_011519097.3:c.713A>G, XM_011519097.2:c.713A>G, XM_011519097.1:c.713A>G, XM_006717304.4:c.713A>G, XM_006717304.3:c.713A>G, XM_006717304.2:c.713A>G, XM_006717304.1:c.713A>G, XM_011519104.4:c.713A>G, XM_011519104.3:c.713A>G, XM_011519104.2:c.713A>G, XM_011519104.1:c.713A>G, NM_032536.4:c.713A>G, NM_032536.3:c.713A>G, NM_032536.2:c.713A>G, XM_011519094.3:c.713A>G, XM_011519094.2:c.713A>G, XM_011519094.1:c.713A>G, XM_011519098.3:c.713A>G, XM_011519098.2:c.713A>G, XM_011519098.1:c.713A>G, XM_011519106.3:c.713A>G, XM_011519106.2:c.713A>G, XM_011519106.1:c.713A>G, XM_011519102.3:c.713A>G, XM_011519102.2:c.713A>G, XM_011519102.1:c.713A>G, XM_011519099.3:c.713A>G, XM_011519099.2:c.713A>G, XM_011519099.1:c.713A>G, XM_011519096.3:c.713A>G, XM_011519096.2:c.713A>G, XM_011519096.1:c.713A>G, XM_011519100.3:c.713A>G, XM_011519100.2:c.713A>G, XM_011519100.1:c.713A>G, XM_011519105.3:c.713A>G, XM_011519105.2:c.713A>G, XM_011519105.1:c.713A>G, XM_011519107.3:c.713A>G, XM_011519107.2:c.713A>G, XM_011519107.1:c.713A>G, XM_011519103.3:c.713A>G, XM_011519103.2:c.713A>G, XM_011519103.1:c.713A>G, XM_011519108.3:c.713A>G, XM_011519108.2:c.713A>G, XM_011519108.1:c.713A>G, XM_011519109.3:c.713A>G, XM_011519109.2:c.713A>G, XM_011519109.1:c.713A>G, XM_011519110.3:c.713A>G, XM_011519110.2:c.713A>G, XM_011519110.1:c.713A>G, XM_017015212.2:c.713A>G, XM_017015212.1:c.713A>G, XM_017015213.2:c.713A>G, XM_017015213.1:c.713A>G, XM_017015216.2:c.713A>G, XM_017015216.1:c.713A>G, XM_047423971.1:c.713A>G, XM_047423970.1:c.713A>G, XP_011517399.1:p.Glu238Gly, XP_006717367.1:p.Glu238Gly, XP_011517406.1:p.Glu238Gly, NP_115925.2:p.Glu238Gly, XP_011517396.1:p.Glu238Gly, XP_011517400.1:p.Glu238Gly, XP_011517408.1:p.Glu238Gly, XP_011517404.1:p.Glu238Gly, XP_011517401.1:p.Glu238Gly, XP_011517398.1:p.Glu238Gly, XP_011517402.1:p.Glu238Gly, XP_011517407.1:p.Glu238Gly, XP_011517409.1:p.Glu238Gly, XP_011517405.1:p.Glu238Gly, XP_011517410.1:p.Glu238Gly, XP_011517411.1:p.Glu238Gly, XP_011517412.1:p.Glu238Gly, XP_016870701.1:p.Glu238Gly, XP_016870702.1:p.Glu238Gly, XP_016870705.1:p.Glu238Gly, XP_047279927.1:p.Glu238Gly, XP_047279926.1:p.Glu238Gly

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