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Items: 1 to 20 of 3575

1.

rs1491277596 has merged into rs10601812 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    AAAAAAAAAAAA>-,AAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA [Show Flanks]
    Chromosome:
    19:34677168 (GRCh38)
    19:35168073 (GRCh37)
    Canonical SPDI:
    NC_000019.10:34677160:AAAAAAAAAAAAAAAAAAA:AAAAAAA,NC_000019.10:34677160:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000019.10:34677160:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:34677160:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:34677160:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:34677160:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:34677160:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:34677160:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:34677160:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:34677160:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34677160:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
    Gene:
    ZNF302 (Varview), SCGB2B2 (Varview), SCGB1B2P (Varview), ZNF807P (Varview)
    Functional Consequence:
    genic_upstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant,5_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    AAAAAAAAAA=0./0 (ALFA)
    AA=0.1452/727 (1000Genomes)
    HGVS:
    NC_000019.10:g.34677168_34677179del, NC_000019.10:g.34677171_34677179del, NC_000019.10:g.34677174_34677179del, NC_000019.10:g.34677175_34677179del, NC_000019.10:g.34677176_34677179del, NC_000019.10:g.34677177_34677179del, NC_000019.10:g.34677178_34677179del, NC_000019.10:g.34677179del, NC_000019.10:g.34677179dup, NC_000019.10:g.34677177_34677179dup, NC_000019.10:g.34677174_34677179dup, NC_000019.9:g.35168073_35168084del, NC_000019.9:g.35168076_35168084del, NC_000019.9:g.35168079_35168084del, NC_000019.9:g.35168080_35168084del, NC_000019.9:g.35168081_35168084del, NC_000019.9:g.35168082_35168084del, NC_000019.9:g.35168083_35168084del, NC_000019.9:g.35168084del, NC_000019.9:g.35168084dup, NC_000019.9:g.35168082_35168084dup, NC_000019.9:g.35168079_35168084dup, NG_033997.1:g.4530_4541del, NG_033997.1:g.4533_4541del, NG_033997.1:g.4536_4541del, NG_033997.1:g.4537_4541del, NG_033997.1:g.4538_4541del, NG_033997.1:g.4539_4541del, NG_033997.1:g.4540_4541del, NG_033997.1:g.4541del, NG_033997.1:g.4541dup, NG_033997.1:g.4539_4541dup, NG_033997.1:g.4536_4541dup, XM_047439093.1:c.-451_-440del, XM_047439093.1:c.-448_-440del, XM_047439093.1:c.-445_-440del, XM_047439093.1:c.-444_-440del, XM_047439093.1:c.-443_-440del, XM_047439093.1:c.-442_-440del, XM_047439093.1:c.-441_-440del, XM_047439093.1:c.-440del, XM_047439093.1:c.-440dup, XM_047439093.1:c.-442_-440dup, XM_047439093.1:c.-445_-440dup, XM_047439094.1:c.-451_-440del, XM_047439094.1:c.-448_-440del, XM_047439094.1:c.-445_-440del, XM_047439094.1:c.-444_-440del, XM_047439094.1:c.-443_-440del, XM_047439094.1:c.-442_-440del, XM_047439094.1:c.-441_-440del, XM_047439094.1:c.-440del, XM_047439094.1:c.-440dup, XM_047439094.1:c.-442_-440dup, XM_047439094.1:c.-445_-440dup, XM_047439096.1:c.-451_-440del, XM_047439096.1:c.-448_-440del, XM_047439096.1:c.-445_-440del, XM_047439096.1:c.-444_-440del, XM_047439096.1:c.-443_-440del, XM_047439096.1:c.-442_-440del, XM_047439096.1:c.-441_-440del, XM_047439096.1:c.-440del, XM_047439096.1:c.-440dup, XM_047439096.1:c.-442_-440dup, XM_047439096.1:c.-445_-440dup

    2.

    rs1490971054 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>G [Show Flanks]
      Chromosome:
      19:34677800 (GRCh38)
      19:35168705 (GRCh37)
      Canonical SPDI:
      NC_000019.10:34677799:C:G
      Gene:
      ZNF302 (Varview), SCGB2B2 (Varview), SCGB1B2P (Varview), ZNF807P (Varview)
      Functional Consequence:
      2KB_upstream_variant,non_coding_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      G=0./0 (ALFA)
      G=0.000004/1 (TOPMED)
      HGVS:
      NC_000019.10:g.34677800C>G, NC_000019.9:g.35168705C>G, NG_033997.1:g.5162C>G, NM_018443.4:c.-125C>G, NM_018443.3:c.-125C>G, NM_018443.2:c.-125C>G, NM_018675.3:c.-372C>G, NM_018675.2:c.-372C>G, NM_001012320.3:c.-102C>G, NM_001012320.2:c.-102C>G, NM_001012320.1:c.-102C>G, NM_001289188.2:c.-131C>G, NM_001289188.1:c.-131C>G, NM_001289189.2:c.-125C>G, NM_001289189.1:c.-125C>G, NM_001289192.2:c.-125C>G, NM_001289192.1:c.-125C>G, NM_001289182.2:c.-372C>G, NM_001289182.1:c.-372C>G, NM_001289187.2:c.-372C>G, NM_001289187.1:c.-372C>G, NM_001289191.2:c.-102C>G, NM_001289191.1:c.-102C>G, NM_001289181.2:c.-125C>G, NM_001289181.1:c.-125C>G, NM_001289184.2:c.-125C>G, NM_001289184.1:c.-125C>G, NM_001289185.2:c.-102C>G, NM_001289185.1:c.-102C>G, NR_110322.2:n.123C>G, NR_110322.1:n.162C>G, XM_011527111.4:c.-102C>G, XM_011527111.3:c.-102C>G, XM_011527111.2:c.-102C>G, XM_017026980.3:c.-102C>G, XM_017026980.2:c.-102C>G, XM_017026980.1:c.-102C>G, XM_024451607.2:c.-372C>G, XM_024451607.1:c.-372C>G, XM_017026986.2:c.-372C>G, XM_017026986.1:c.-372C>G, XM_024451606.2:c.-125C>G, XM_024451606.1:c.-125C>G, XM_017026978.2:c.-372C>G, XM_017026978.1:c.-372C>G, XM_017026979.2:c.-372C>G, XM_017026979.1:c.-372C>G, XM_017026983.2:c.-102C>G, XM_017026983.1:c.-102C>G, XM_017026985.2:c.-102C>G, XM_017026985.1:c.-102C>G, XM_024451603.2:c.-125C>G, XM_024451603.1:c.-125C>G

      3.

      rs1490743667 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>G [Show Flanks]
        Chromosome:
        19:34685141 (GRCh38)
        19:35176046 (GRCh37)
        Canonical SPDI:
        NC_000019.10:34685140:A:G
        Gene:
        ZNF302 (Varview)
        Functional Consequence:
        non_coding_transcript_variant,synonymous_variant,3_prime_UTR_variant,coding_sequence_variant
        Validated:
        by frequency
        MAF:
        G=0.000004/1 (GnomAD_exomes)
        HGVS:
        NC_000019.10:g.34685141A>G, NC_000019.9:g.35176046A>G, NG_033997.1:g.12503A>G, NM_018443.4:c.1104A>G, NM_018443.3:c.1104A>G, NM_018443.2:c.1104A>G, NM_018675.3:c.*968A>G, NM_018675.2:c.*968A>G, NM_018675.1:c.1341A>G, NM_001012320.3:c.1104A>G, NM_001012320.2:c.1104A>G, NM_001012320.1:c.1104A>G, NM_001289188.2:c.*968A>G, NM_001289188.1:c.*968A>G, NM_001289189.2:c.*968A>G, NM_001289189.1:c.*968A>G, NM_001289192.2:c.*968A>G, NM_001289192.1:c.*968A>G, NM_001289182.2:c.1107A>G, NM_001289182.1:c.1107A>G, NM_001289187.2:c.1104A>G, NM_001289187.1:c.1104A>G, NM_001289191.2:c.*968A>G, NM_001289191.1:c.*968A>G, NM_001289190.2:c.*968A>G, NM_001289190.1:c.*968A>G, NM_001289181.2:c.1236A>G, NM_001289181.1:c.1236A>G, NM_001289184.2:c.1107A>G, NM_001289184.1:c.1107A>G, NM_001289185.2:c.1107A>G, NM_001289185.1:c.1107A>G, NM_001289183.2:c.1104A>G, NM_001289183.1:c.1104A>G, NM_001289186.2:c.1104A>G, NM_001289186.1:c.1104A>G, NR_110322.2:n.1146A>G, NR_110322.1:n.1185A>G, XM_011527111.4:c.*968A>G, XM_011527111.3:c.*968A>G, XM_011527111.2:c.*968A>G, XM_011527111.1:c.*968A>G, XM_017026980.3:c.1236A>G, XM_017026980.2:c.1236A>G, XM_017026980.1:c.1236A>G, XM_017026981.3:c.1236A>G, XM_017026981.2:c.1236A>G, XM_017026981.1:c.1236A>G, XM_024451607.2:c.*968A>G, XM_017026986.2:c.*968A>G, XM_017026986.1:c.*968A>G, XM_024451606.2:c.*968A>G, XM_017026978.2:c.1239A>G, XM_017026978.1:c.1239A>G, XM_017026979.2:c.1236A>G, XM_017026979.1:c.1236A>G, XM_017026983.2:c.*968A>G, XM_017026985.2:c.*968A>G, XM_024451603.2:c.1239A>G, XM_024451603.1:c.1239A>G, XM_017026982.2:c.1107A>G, XM_017026982.1:c.1107A>G, XM_047439093.1:c.1236A>G, XM_047439094.1:c.1107A>G, XM_047439096.1:c.1104A>G, XM_047439097.1:c.1104A>G, XM_047439095.1:c.1107A>G

        4.

        rs1490532992 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          A>G [Show Flanks]
          Chromosome:
          19:34676802 (GRCh38)
          19:35167707 (GRCh37)
          Canonical SPDI:
          NC_000019.10:34676801:A:G
          Gene:
          ZNF302 (Varview), SCGB2B2 (Varview), SCGB1B2P (Varview), ZNF807P (Varview)
          Functional Consequence:
          non_coding_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,genic_upstream_transcript_variant
          Validated:
          by frequency,by alfa
          MAF:
          G=0./0 (ALFA)
          HGVS:

          5.

          rs1490508770 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>T [Show Flanks]
            Chromosome:
            19:34677729 (GRCh38)
            19:35168634 (GRCh37)
            Canonical SPDI:
            NC_000019.10:34677728:G:T
            Gene:
            ZNF302 (Varview), SCGB2B2 (Varview), SCGB1B2P (Varview), ZNF807P (Varview)
            Functional Consequence:
            2KB_upstream_variant,non_coding_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            T=0./0 (ALFA)
            T=0.000004/1 (TOPMED)
            HGVS:
            NC_000019.10:g.34677729G>T, NC_000019.9:g.35168634G>T, NG_033997.1:g.5091G>T, NM_018443.4:c.-196G>T, NM_018443.3:c.-196G>T, NM_018443.2:c.-196G>T, NM_018675.3:c.-443G>T, NM_018675.2:c.-443G>T, NM_001012320.3:c.-173G>T, NM_001012320.2:c.-173G>T, NM_001012320.1:c.-173G>T, NM_001289188.2:c.-202G>T, NM_001289188.1:c.-202G>T, NM_001289189.2:c.-196G>T, NM_001289189.1:c.-196G>T, NM_001289192.2:c.-196G>T, NM_001289192.1:c.-196G>T, NM_001289182.2:c.-443G>T, NM_001289182.1:c.-443G>T, NM_001289187.2:c.-443G>T, NM_001289187.1:c.-443G>T, NM_001289191.2:c.-173G>T, NM_001289191.1:c.-173G>T, NM_001289190.2:c.-136G>T, NM_001289190.1:c.-136G>T, NM_001289181.2:c.-196G>T, NM_001289181.1:c.-196G>T, NM_001289184.2:c.-196G>T, NM_001289184.1:c.-196G>T, NM_001289185.2:c.-173G>T, NM_001289185.1:c.-173G>T, NM_001289183.2:c.-136G>T, NM_001289183.1:c.-136G>T, NM_001289186.2:c.-94G>T, NM_001289186.1:c.-94G>T, NR_110322.2:n.52G>T, NR_110322.1:n.91G>T, XM_011527111.4:c.-173G>T, XM_011527111.3:c.-173G>T, XM_011527111.2:c.-173G>T, XM_017026980.3:c.-173G>T, XM_017026980.2:c.-173G>T, XM_017026980.1:c.-173G>T, XM_017026981.3:c.-136G>T, XM_017026981.2:c.-136G>T, XM_017026981.1:c.-136G>T, XM_024451607.2:c.-443G>T, XM_024451607.1:c.-443G>T, XM_017026986.2:c.-443G>T, XM_017026986.1:c.-443G>T, XM_024451606.2:c.-196G>T, XM_024451606.1:c.-196G>T, XM_017026978.2:c.-443G>T, XM_017026978.1:c.-443G>T, XM_017026979.2:c.-443G>T, XM_017026979.1:c.-443G>T, XM_017026983.2:c.-173G>T, XM_017026983.1:c.-173G>T, XM_017026985.2:c.-173G>T, XM_017026985.1:c.-173G>T, XM_024451603.2:c.-196G>T, XM_024451603.1:c.-196G>T, XM_017026982.2:c.-136G>T, XM_017026982.1:c.-136G>T

            6.

            rs1490477993 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              G>A [Show Flanks]
              Chromosome:
              19:34678616 (GRCh38)
              19:35169521 (GRCh37)
              Canonical SPDI:
              NC_000019.10:34678615:G:A
              Gene:
              ZNF302 (Varview), SCGB2B2 (Varview), SCGB1B2P (Varview), ZNF807P (Varview)
              Functional Consequence:
              2KB_upstream_variant,upstream_transcript_variant,intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              A=0.000071/1 (ALFA)
              A=0.000011/3 (TOPMED)
              A=0.000014/2 (GnomAD)
              HGVS:

              7.

              rs1490052394 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>C [Show Flanks]
                Chromosome:
                19:34679358 (GRCh38)
                19:35170263 (GRCh37)
                Canonical SPDI:
                NC_000019.10:34679357:T:C
                Gene:
                ZNF302 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                C=0./0 (ALFA)
                C=0.000004/1 (TOPMED)
                C=0.000007/1 (GnomAD)
                HGVS:

                8.

                rs1489980062 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  TAAA>- [Show Flanks]
                  Chromosome:
                  19:34686341 (GRCh38)
                  19:35177246 (GRCh37)
                  Canonical SPDI:
                  NC_000019.10:34686337:AAATAAA:AAA
                  Gene:
                  ZNF302 (Varview)
                  Functional Consequence:
                  non_coding_transcript_variant,3_prime_UTR_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  AAA=0.000071/1 (ALFA)
                  -=0.000007/1 (GnomAD)
                  -=0.000008/2 (TOPMED)
                  -=0.000156/1 (1000Genomes)
                  HGVS:
                  NC_000019.10:g.34686341_34686344del, NC_000019.9:g.35177246_35177249del, NG_033997.1:g.13703_13706del, NM_018443.4:c.*1104_*1107del, NM_018443.3:c.*1104_*1107del, NM_018443.2:c.*1104_*1107del, NM_018675.3:c.*2168_*2171del, NM_018675.2:c.*2168_*2171del, NM_018675.1:c.*1106_*1109del, NM_001012320.3:c.*1104_*1107del, NM_001012320.2:c.*1104_*1107del, NM_001012320.1:c.*1104_*1107del, NM_001289188.2:c.*2168_*2171del, NM_001289188.1:c.*2168_*2171del, NM_001289189.2:c.*2168_*2171del, NM_001289189.1:c.*2168_*2171del, NM_001289192.2:c.*2168_*2171del, NM_001289192.1:c.*2168_*2171del, NM_001289182.2:c.*1104_*1107del, NM_001289182.1:c.*1104_*1107del, NM_001289187.2:c.*1104_*1107del, NM_001289187.1:c.*1104_*1107del, NM_001289191.2:c.*2168_*2171del, NM_001289191.1:c.*2168_*2171del, NM_001289190.2:c.*2168_*2171del, NM_001289190.1:c.*2168_*2171del, NM_001289181.2:c.*1104_*1107del, NM_001289181.1:c.*1104_*1107del, NM_001289184.2:c.*1104_*1107del, NM_001289184.1:c.*1104_*1107del, NM_001289185.2:c.*1104_*1107del, NM_001289185.1:c.*1104_*1107del, NM_001289183.2:c.*1104_*1107del, NM_001289183.1:c.*1104_*1107del, NM_001289186.2:c.*1104_*1107del, NM_001289186.1:c.*1104_*1107del, NR_110322.2:n.2346_2349del, NR_110322.1:n.2385_2388del, XM_011527111.4:c.*2168_*2171del, XM_011527111.3:c.*2168_*2171del, XM_011527111.2:c.*2168_*2171del, XM_011527111.1:c.*2168_*2171del, XM_017026980.3:c.*1104_*1107del, XM_017026980.2:c.*1104_*1107del, XM_017026980.1:c.*1104_*1107del, XM_017026981.3:c.*1104_*1107del, XM_017026981.2:c.*1104_*1107del, XM_017026981.1:c.*1104_*1107del, XM_024451607.2:c.*2168_*2171del, XM_017026986.2:c.*2168_*2171del, XM_017026986.1:c.*2168_*2171del, XM_024451606.2:c.*2168_*2171del, XM_017026978.2:c.*1104_*1107del, XM_017026978.1:c.*1104_*1107del, XM_017026979.2:c.*1104_*1107del, XM_017026979.1:c.*1104_*1107del, XM_017026983.2:c.*2168_*2171del, XM_017026985.2:c.*2168_*2171del, XM_024451603.2:c.*1104_*1107del, XM_024451603.1:c.*1104_*1107del, XM_017026982.2:c.*1104_*1107del, XM_017026982.1:c.*1104_*1107del, XM_047439093.1:c.*1104_*1107del, XM_047439094.1:c.*1104_*1107del, XM_047439096.1:c.*1104_*1107del, XM_047439097.1:c.*1104_*1107del, XM_047439095.1:c.*1104_*1107del

                  9.

                  rs1489956550 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    T>A [Show Flanks]
                    Chromosome:
                    19:34687397 (GRCh38)
                    19:35178302 (GRCh37)
                    Canonical SPDI:
                    NC_000019.10:34687396:T:A
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    A=0./0 (ALFA)
                    A=0.000008/2 (TOPMED)
                    A=0.000014/2 (GnomAD)
                    HGVS:

                    10.

                    rs1489896563 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>T [Show Flanks]
                      Chromosome:
                      19:34682146 (GRCh38)
                      19:35173051 (GRCh37)
                      Canonical SPDI:
                      NC_000019.10:34682145:C:T
                      Gene:
                      ZNF302 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      T=0.000071/1 (ALFA)
                      T=0.000004/1 (TOPMED)
                      HGVS:

                      11.

                      rs1489569554 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        A>G [Show Flanks]
                        Chromosome:
                        19:34688275 (GRCh38)
                        19:35179180 (GRCh37)
                        Canonical SPDI:
                        NC_000019.10:34688274:A:G
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        G=0./0 (ALFA)
                        G=0.000004/1 (TOPMED)
                        G=0.000007/1 (GnomAD)
                        HGVS:

                        12.

                        rs1489208975 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          19:34681003 (GRCh38)
                          19:35171908 (GRCh37)
                          Canonical SPDI:
                          NC_000019.10:34681002:C:T
                          Gene:
                          ZNF302 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          T=0.0018/8 (ALFA)
                          HGVS:

                          13.

                          rs1488876431 has merged into rs746866893 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                            Chromosome:
                            19:34684181 (GRCh38)
                            19:35175086 (GRCh37)
                            Canonical SPDI:
                            NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:34684171:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                            Gene:
                            ZNF302 (Varview)
                            Functional Consequence:
                            intron_variant,3_prime_UTR_variant,terminator_codon_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            AAAAAAAAAAAA=0./0 (ALFA)
                            AAAAAAAAAAAAAAAAA=0.4/16 (GENOME_DK)
                            HGVS:
                            NC_000019.10:g.34684181_34684220del, NC_000019.10:g.34684183_34684220del, NC_000019.10:g.34684184_34684220del, NC_000019.10:g.34684185_34684220del, NC_000019.10:g.34684186_34684220del, NC_000019.10:g.34684187_34684220del, NC_000019.10:g.34684188_34684220del, NC_000019.10:g.34684189_34684220del, NC_000019.10:g.34684190_34684220del, NC_000019.10:g.34684191_34684220del, NC_000019.10:g.34684192_34684220del, NC_000019.10:g.34684193_34684220del, NC_000019.10:g.34684194_34684220del, NC_000019.10:g.34684195_34684220del, NC_000019.10:g.34684196_34684220del, NC_000019.10:g.34684197_34684220del, NC_000019.10:g.34684198_34684220del, NC_000019.10:g.34684199_34684220del, NC_000019.10:g.34684200_34684220del, NC_000019.10:g.34684201_34684220del, NC_000019.10:g.34684202_34684220del, NC_000019.10:g.34684203_34684220del, NC_000019.10:g.34684204_34684220del, NC_000019.10:g.34684205_34684220del, NC_000019.10:g.34684206_34684220del, NC_000019.10:g.34684207_34684220del, NC_000019.10:g.34684208_34684220del, NC_000019.10:g.34684209_34684220del, NC_000019.10:g.34684210_34684220del, NC_000019.10:g.34684211_34684220del, NC_000019.10:g.34684213_34684220del, NC_000019.10:g.34684214_34684220del, NC_000019.10:g.34684215_34684220del, NC_000019.10:g.34684220del, NC_000019.10:g.34684220dup, NC_000019.10:g.34684216_34684220dup, NC_000019.10:g.34684214_34684220dup, NC_000019.10:g.34684210_34684220dup, NC_000019.10:g.34684209_34684220dup, NC_000019.9:g.35175086_35175125del, NC_000019.9:g.35175088_35175125del, NC_000019.9:g.35175089_35175125del, NC_000019.9:g.35175090_35175125del, NC_000019.9:g.35175091_35175125del, NC_000019.9:g.35175092_35175125del, NC_000019.9:g.35175093_35175125del, NC_000019.9:g.35175094_35175125del, NC_000019.9:g.35175095_35175125del, NC_000019.9:g.35175096_35175125del, NC_000019.9:g.35175097_35175125del, NC_000019.9:g.35175098_35175125del, NC_000019.9:g.35175099_35175125del, NC_000019.9:g.35175100_35175125del, NC_000019.9:g.35175101_35175125del, NC_000019.9:g.35175102_35175125del, NC_000019.9:g.35175103_35175125del, NC_000019.9:g.35175104_35175125del, NC_000019.9:g.35175105_35175125del, NC_000019.9:g.35175106_35175125del, NC_000019.9:g.35175107_35175125del, NC_000019.9:g.35175108_35175125del, NC_000019.9:g.35175109_35175125del, NC_000019.9:g.35175110_35175125del, NC_000019.9:g.35175111_35175125del, NC_000019.9:g.35175112_35175125del, NC_000019.9:g.35175113_35175125del, NC_000019.9:g.35175114_35175125del, NC_000019.9:g.35175115_35175125del, NC_000019.9:g.35175116_35175125del, NC_000019.9:g.35175118_35175125del, NC_000019.9:g.35175119_35175125del, NC_000019.9:g.35175120_35175125del, NC_000019.9:g.35175125del, NC_000019.9:g.35175125dup, NC_000019.9:g.35175121_35175125dup, NC_000019.9:g.35175119_35175125dup, NC_000019.9:g.35175115_35175125dup, NC_000019.9:g.35175114_35175125dup, NG_033997.1:g.11543_11582del, NG_033997.1:g.11545_11582del, NG_033997.1:g.11546_11582del, NG_033997.1:g.11547_11582del, NG_033997.1:g.11548_11582del, NG_033997.1:g.11549_11582del, NG_033997.1:g.11550_11582del, NG_033997.1:g.11551_11582del, NG_033997.1:g.11552_11582del, NG_033997.1:g.11553_11582del, NG_033997.1:g.11554_11582del, NG_033997.1:g.11555_11582del, NG_033997.1:g.11556_11582del, NG_033997.1:g.11557_11582del, NG_033997.1:g.11558_11582del, NG_033997.1:g.11559_11582del, NG_033997.1:g.11560_11582del, NG_033997.1:g.11561_11582del, NG_033997.1:g.11562_11582del, NG_033997.1:g.11563_11582del, NG_033997.1:g.11564_11582del, NG_033997.1:g.11565_11582del, NG_033997.1:g.11566_11582del, NG_033997.1:g.11567_11582del, NG_033997.1:g.11568_11582del, NG_033997.1:g.11569_11582del, NG_033997.1:g.11570_11582del, NG_033997.1:g.11571_11582del, NG_033997.1:g.11572_11582del, NG_033997.1:g.11573_11582del, NG_033997.1:g.11575_11582del, NG_033997.1:g.11576_11582del, NG_033997.1:g.11577_11582del, NG_033997.1:g.11582del, NG_033997.1:g.11582dup, NG_033997.1:g.11578_11582dup, NG_033997.1:g.11576_11582dup, NG_033997.1:g.11572_11582dup, NG_033997.1:g.11571_11582dup, NM_018675.3:c.*8_*47del, NM_018675.3:c.*10_*47del, NM_018675.3:c.*11_*47del, NM_018675.3:c.*12_*47del, NM_018675.3:c.*13_*47del, NM_018675.3:c.*14_*47del, NM_018675.3:c.*15_*47del, NM_018675.3:c.*16_*47del, NM_018675.3:c.*17_*47del, NM_018675.3:c.*18_*47del, NM_018675.3:c.*19_*47del, NM_018675.3:c.*20_*47del, NM_018675.3:c.*21_*47del, NM_018675.3:c.*22_*47del, NM_018675.3:c.*23_*47del, NM_018675.3:c.*24_*47del, NM_018675.3:c.*25_*47del, NM_018675.3:c.*26_*47del, NM_018675.3:c.*27_*47del, NM_018675.3:c.*28_*47del, NM_018675.3:c.*29_*47del, NM_018675.3:c.*30_*47del, NM_018675.3:c.*31_*47del, NM_018675.3:c.*32_*47del, NM_018675.3:c.*33_*47del, NM_018675.3:c.*34_*47del, NM_018675.3:c.*35_*47del, NM_018675.3:c.*36_*47del, NM_018675.3:c.*37_*47del, NM_018675.3:c.*38_*47del, NM_018675.3:c.*40_*47del, NM_018675.3:c.*41_*47del, NM_018675.3:c.*42_*47del, NM_018675.3:c.*47del, NM_018675.3:c.*47dup, NM_018675.3:c.*43_*47dup, NM_018675.3:c.*41_*47dup, NM_018675.3:c.*37_*47dup, NM_018675.3:c.*36_*47dup, NM_018675.2:c.*8_*47del, NM_018675.2:c.*10_*47del, NM_018675.2:c.*11_*47del, NM_018675.2:c.*12_*47del, NM_018675.2:c.*13_*47del, NM_018675.2:c.*14_*47del, NM_018675.2:c.*15_*47del, NM_018675.2:c.*16_*47del, NM_018675.2:c.*17_*47del, NM_018675.2:c.*18_*47del, NM_018675.2:c.*19_*47del, NM_018675.2:c.*20_*47del, NM_018675.2:c.*21_*47del, NM_018675.2:c.*22_*47del, NM_018675.2:c.*23_*47del, NM_018675.2:c.*24_*47del, NM_018675.2:c.*25_*47del, NM_018675.2:c.*26_*47del, NM_018675.2:c.*27_*47del, NM_018675.2:c.*28_*47del, NM_018675.2:c.*29_*47del, NM_018675.2:c.*30_*47del, NM_018675.2:c.*31_*47del, NM_018675.2:c.*32_*47del, NM_018675.2:c.*33_*47del, NM_018675.2:c.*34_*47del, NM_018675.2:c.*35_*47del, NM_018675.2:c.*36_*47del, NM_018675.2:c.*37_*47del, NM_018675.2:c.*38_*47del, NM_018675.2:c.*40_*47del, NM_018675.2:c.*41_*47del, NM_018675.2:c.*42_*47del, NM_018675.2:c.*47del, NM_018675.2:c.*47dup, NM_018675.2:c.*43_*47dup, NM_018675.2:c.*41_*47dup, NM_018675.2:c.*37_*47dup, NM_018675.2:c.*36_*47dup, NM_018675.1:c.401_421dup, NM_018675.1:c.403_421del, NM_018675.1:c.405_421del, NM_018675.1:c.406_421del, NM_018675.1:c.407_421del, NM_018675.1:c.408_421del, NM_018675.1:c.409_421del, NM_018675.1:c.410_421del, NM_018675.1:c.411_421del, NM_018675.1:c.412_421del, NM_018675.1:c.413_421del, NM_018675.1:c.414_421del, NM_018675.1:c.415_421del, NM_018675.1:c.416_421del, NM_018675.1:c.417_421del, NM_018675.1:c.418_421del, NM_018675.1:c.419_421del, NM_018675.1:c.420_421del, NM_018675.1:c.421del, NM_018675.1:c.421dup, NM_018675.1:c.420_421dup, NM_018675.1:c.419_421dup, NM_018675.1:c.418_421dup, NM_018675.1:c.417_421dup, NM_018675.1:c.416_421dup, NM_018675.1:c.415_421dup, NM_018675.1:c.414_421dup, NM_018675.1:c.413_421dup, NM_018675.1:c.412_421dup, NM_018675.1:c.411_421dup, NM_018675.1:c.409_421dup, NM_018675.1:c.408_421dup, NM_018675.1:c.407_421dup, NM_018675.1:c.402_421dup, NM_018675.1:c.400_421dup, NM_018675.1:c.396_421dup, NM_018675.1:c.394_421dup, NM_018675.1:c.421_422insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_018675.1:c.421_422insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001289188.2:c.*8_*47del, NM_001289188.2:c.*10_*47del, NM_001289188.2:c.*11_*47del, NM_001289188.2:c.*12_*47del, NM_001289188.2:c.*13_*47del, NM_001289188.2:c.*14_*47del, NM_001289188.2:c.*15_*47del, NM_001289188.2:c.*16_*47del, NM_001289188.2:c.*17_*47del, NM_001289188.2:c.*18_*47del, NM_001289188.2:c.*19_*47del, NM_001289188.2:c.*20_*47del, NM_001289188.2:c.*21_*47del, NM_001289188.2:c.*22_*47del, NM_001289188.2:c.*23_*47del, NM_001289188.2:c.*24_*47del, NM_001289188.2:c.*25_*47del, NM_001289188.2:c.*26_*47del, NM_001289188.2:c.*27_*47del, NM_001289188.2:c.*28_*47del, NM_001289188.2:c.*29_*47del, NM_001289188.2:c.*30_*47del, NM_001289188.2:c.*31_*47del, NM_001289188.2:c.*32_*47del, NM_001289188.2:c.*33_*47del, NM_001289188.2:c.*34_*47del, NM_001289188.2:c.*35_*47del, NM_001289188.2:c.*36_*47del, NM_001289188.2:c.*37_*47del, NM_001289188.2:c.*38_*47del, NM_001289188.2:c.*40_*47del, NM_001289188.2:c.*41_*47del, NM_001289188.2:c.*42_*47del, NM_001289188.2:c.*47del, NM_001289188.2:c.*47dup, NM_001289188.2:c.*43_*47dup, NM_001289188.2:c.*41_*47dup, NM_001289188.2:c.*37_*47dup, NM_001289188.2:c.*36_*47dup, NM_001289188.1:c.*8_*47del, NM_001289188.1:c.*10_*47del, NM_001289188.1:c.*11_*47del, NM_001289188.1:c.*12_*47del, NM_001289188.1:c.*13_*47del, NM_001289188.1:c.*14_*47del, NM_001289188.1:c.*15_*47del, NM_001289188.1:c.*16_*47del, NM_001289188.1:c.*17_*47del, NM_001289188.1:c.*18_*47del, NM_001289188.1:c.*19_*47del, NM_001289188.1:c.*20_*47del, NM_001289188.1:c.*21_*47del, NM_001289188.1:c.*22_*47del, NM_001289188.1:c.*23_*47del, NM_001289188.1:c.*24_*47del, NM_001289188.1:c.*25_*47del, NM_001289188.1:c.*26_*47del, NM_001289188.1:c.*27_*47del, NM_001289188.1:c.*28_*47del, NM_001289188.1:c.*29_*47del, NM_001289188.1:c.*30_*47del, NM_001289188.1:c.*31_*47del, NM_001289188.1:c.*32_*47del, NM_001289188.1:c.*33_*47del, NM_001289188.1:c.*34_*47del, NM_001289188.1:c.*35_*47del, NM_001289188.1:c.*36_*47del, NM_001289188.1:c.*37_*47del, NM_001289188.1:c.*38_*47del, NM_001289188.1:c.*40_*47del, NM_001289188.1:c.*41_*47del, NM_001289188.1:c.*42_*47del, NM_001289188.1:c.*47del, NM_001289188.1:c.*47dup, NM_001289188.1:c.*43_*47dup, NM_001289188.1:c.*41_*47dup, NM_001289188.1:c.*37_*47dup, NM_001289188.1:c.*36_*47dup, NM_001289189.2:c.*8_*47del, NM_001289189.2:c.*10_*47del, NM_001289189.2:c.*11_*47del, NM_001289189.2:c.*12_*47del, NM_001289189.2:c.*13_*47del, NM_001289189.2:c.*14_*47del, NM_001289189.2:c.*15_*47del, NM_001289189.2:c.*16_*47del, NM_001289189.2:c.*17_*47del, NM_001289189.2:c.*18_*47del, NM_001289189.2:c.*19_*47del, NM_001289189.2:c.*20_*47del, NM_001289189.2:c.*21_*47del, NM_001289189.2:c.*22_*47del, NM_001289189.2:c.*23_*47del, NM_001289189.2:c.*24_*47del, NM_001289189.2:c.*25_*47del, NM_001289189.2:c.*26_*47del, NM_001289189.2:c.*27_*47del, NM_001289189.2:c.*28_*47del, NM_001289189.2:c.*29_*47del, NM_001289189.2:c.*30_*47del, NM_001289189.2:c.*31_*47del, NM_001289189.2:c.*32_*47del, NM_001289189.2:c.*33_*47del, NM_001289189.2:c.*34_*47del, NM_001289189.2:c.*35_*47del, NM_001289189.2:c.*36_*47del, NM_001289189.2:c.*37_*47del, NM_001289189.2:c.*38_*47del, NM_001289189.2:c.*40_*47del, NM_001289189.2:c.*41_*47del, NM_001289189.2:c.*42_*47del, NM_001289189.2:c.*47del, NM_001289189.2:c.*47dup, NM_001289189.2:c.*43_*47dup, NM_001289189.2:c.*41_*47dup, NM_001289189.2:c.*37_*47dup, NM_001289189.2:c.*36_*47dup, NM_001289189.1:c.*8_*47del, NM_001289189.1:c.*10_*47del, NM_001289189.1:c.*11_*47del, NM_001289189.1:c.*12_*47del, NM_001289189.1:c.*13_*47del, NM_001289189.1:c.*14_*47del, NM_001289189.1:c.*15_*47del, NM_001289189.1:c.*16_*47del, NM_001289189.1:c.*17_*47del, NM_001289189.1:c.*18_*47del, NM_001289189.1:c.*19_*47del, NM_001289189.1:c.*20_*47del, NM_001289189.1:c.*21_*47del, NM_001289189.1:c.*22_*47del, NM_001289189.1:c.*23_*47del, NM_001289189.1:c.*24_*47del, NM_001289189.1:c.*25_*47del, NM_001289189.1:c.*26_*47del, NM_001289189.1:c.*27_*47del, NM_001289189.1:c.*28_*47del, NM_001289189.1:c.*29_*47del, NM_001289189.1:c.*30_*47del, NM_001289189.1:c.*31_*47del, NM_001289189.1:c.*32_*47del, NM_001289189.1:c.*33_*47del, NM_001289189.1:c.*34_*47del, NM_001289189.1:c.*35_*47del, NM_001289189.1:c.*36_*47del, NM_001289189.1:c.*37_*47del, NM_001289189.1:c.*38_*47del, NM_001289189.1:c.*40_*47del, NM_001289189.1:c.*41_*47del, NM_001289189.1:c.*42_*47del, NM_001289189.1:c.*47del, NM_001289189.1:c.*47dup, NM_001289189.1:c.*43_*47dup, NM_001289189.1:c.*41_*47dup, NM_001289189.1:c.*37_*47dup, NM_001289189.1:c.*36_*47dup, NM_001289192.2:c.*8_*47del, NM_001289192.2:c.*10_*47del, NM_001289192.2:c.*11_*47del, NM_001289192.2:c.*12_*47del, NM_001289192.2:c.*13_*47del, NM_001289192.2:c.*14_*47del, NM_001289192.2:c.*15_*47del, NM_001289192.2:c.*16_*47del, NM_001289192.2:c.*17_*47del, NM_001289192.2:c.*18_*47del, NM_001289192.2:c.*19_*47del, NM_001289192.2:c.*20_*47del, NM_001289192.2:c.*21_*47del, NM_001289192.2:c.*22_*47del, NM_001289192.2:c.*23_*47del, NM_001289192.2:c.*24_*47del, NM_001289192.2:c.*25_*47del, NM_001289192.2:c.*26_*47del, NM_001289192.2:c.*27_*47del, NM_001289192.2:c.*28_*47del, NM_001289192.2:c.*29_*47del, NM_001289192.2:c.*30_*47del, NM_001289192.2:c.*31_*47del, NM_001289192.2:c.*32_*47del, NM_001289192.2:c.*33_*47del, NM_001289192.2:c.*34_*47del, NM_001289192.2:c.*35_*47del, NM_001289192.2:c.*36_*47del, NM_001289192.2:c.*37_*47del, NM_001289192.2:c.*38_*47del, NM_001289192.2:c.*40_*47del, NM_001289192.2:c.*41_*47del, NM_001289192.2:c.*42_*47del, NM_001289192.2:c.*47del, NM_001289192.2:c.*47dup, NM_001289192.2:c.*43_*47dup, NM_001289192.2:c.*41_*47dup, NM_001289192.2:c.*37_*47dup, NM_001289192.2:c.*36_*47dup, NM_001289192.1:c.*8_*47del, NM_001289192.1:c.*10_*47del, NM_001289192.1:c.*11_*47del, NM_001289192.1:c.*12_*47del, NM_001289192.1:c.*13_*47del, NM_001289192.1:c.*14_*47del, NM_001289192.1:c.*15_*47del, NM_001289192.1:c.*16_*47del, NM_001289192.1:c.*17_*47del, NM_001289192.1:c.*18_*47del, NM_001289192.1:c.*19_*47del, NM_001289192.1:c.*20_*47del, NM_001289192.1:c.*21_*47del, NM_001289192.1:c.*22_*47del, NM_001289192.1:c.*23_*47del, NM_001289192.1:c.*24_*47del, NM_001289192.1:c.*25_*47del, NM_001289192.1:c.*26_*47del, NM_001289192.1:c.*27_*47del, NM_001289192.1:c.*28_*47del, NM_001289192.1:c.*29_*47del, NM_001289192.1:c.*30_*47del, NM_001289192.1:c.*31_*47del, NM_001289192.1:c.*32_*47del, NM_001289192.1:c.*33_*47del, NM_001289192.1:c.*34_*47del, NM_001289192.1:c.*35_*47del, NM_001289192.1:c.*36_*47del, NM_001289192.1:c.*37_*47del, NM_001289192.1:c.*38_*47del, NM_001289192.1:c.*40_*47del, NM_001289192.1:c.*41_*47del, NM_001289192.1:c.*42_*47del, NM_001289192.1:c.*47del, NM_001289192.1:c.*47dup, NM_001289192.1:c.*43_*47dup, NM_001289192.1:c.*41_*47dup, NM_001289192.1:c.*37_*47dup, NM_001289192.1:c.*36_*47dup, NM_001289191.2:c.*8_*47del, NM_001289191.2:c.*10_*47del, NM_001289191.2:c.*11_*47del, NM_001289191.2:c.*12_*47del, NM_001289191.2:c.*13_*47del, NM_001289191.2:c.*14_*47del, NM_001289191.2:c.*15_*47del, NM_001289191.2:c.*16_*47del, NM_001289191.2:c.*17_*47del, NM_001289191.2:c.*18_*47del, NM_001289191.2:c.*19_*47del, NM_001289191.2:c.*20_*47del, NM_001289191.2:c.*21_*47del, NM_001289191.2:c.*22_*47del, NM_001289191.2:c.*23_*47del, NM_001289191.2:c.*24_*47del, NM_001289191.2:c.*25_*47del, NM_001289191.2:c.*26_*47del, NM_001289191.2:c.*27_*47del, NM_001289191.2:c.*28_*47del, NM_001289191.2:c.*29_*47del, NM_001289191.2:c.*30_*47del, NM_001289191.2:c.*31_*47del, NM_001289191.2:c.*32_*47del, NM_001289191.2:c.*33_*47del, NM_001289191.2:c.*34_*47del, NM_001289191.2:c.*35_*47del, NM_001289191.2:c.*36_*47del, NM_001289191.2:c.*37_*47del, NM_001289191.2:c.*38_*47del, NM_001289191.2:c.*40_*47del, NM_001289191.2:c.*41_*47del, NM_001289191.2:c.*42_*47del, NM_001289191.2:c.*47del, NM_001289191.2:c.*47dup, NM_001289191.2:c.*43_*47dup, NM_001289191.2:c.*41_*47dup, NM_001289191.2:c.*37_*47dup, NM_001289191.2:c.*36_*47dup, NM_001289191.1:c.*8_*47del, NM_001289191.1:c.*10_*47del, NM_001289191.1:c.*11_*47del, NM_001289191.1:c.*12_*47del, NM_001289191.1:c.*13_*47del, NM_001289191.1:c.*14_*47del, NM_001289191.1:c.*15_*47del, NM_001289191.1:c.*16_*47del, NM_001289191.1:c.*17_*47del, NM_001289191.1:c.*18_*47del, NM_001289191.1:c.*19_*47del, NM_001289191.1:c.*20_*47del, NM_001289191.1:c.*21_*47del, NM_001289191.1:c.*22_*47del, NM_001289191.1:c.*23_*47del, NM_001289191.1:c.*24_*47del, NM_001289191.1:c.*25_*47del, NM_001289191.1:c.*26_*47del, NM_001289191.1:c.*27_*47del, NM_001289191.1:c.*28_*47del, NM_001289191.1:c.*29_*47del, NM_001289191.1:c.*30_*47del, NM_001289191.1:c.*31_*47del, NM_001289191.1:c.*32_*47del, NM_001289191.1:c.*33_*47del, NM_001289191.1:c.*34_*47del, NM_001289191.1:c.*35_*47del, NM_001289191.1:c.*36_*47del, NM_001289191.1:c.*37_*47del, NM_001289191.1:c.*38_*47del, NM_001289191.1:c.*40_*47del, NM_001289191.1:c.*41_*47del, NM_001289191.1:c.*42_*47del, NM_001289191.1:c.*47del, NM_001289191.1:c.*47dup, NM_001289191.1:c.*43_*47dup, NM_001289191.1:c.*41_*47dup, NM_001289191.1:c.*37_*47dup, NM_001289191.1:c.*36_*47dup, NM_001289190.2:c.*8_*47del, NM_001289190.2:c.*10_*47del, NM_001289190.2:c.*11_*47del, NM_001289190.2:c.*12_*47del, NM_001289190.2:c.*13_*47del, NM_001289190.2:c.*14_*47del, NM_001289190.2:c.*15_*47del, NM_001289190.2:c.*16_*47del, NM_001289190.2:c.*17_*47del, NM_001289190.2:c.*18_*47del, NM_001289190.2:c.*19_*47del, NM_001289190.2:c.*20_*47del, NM_001289190.2:c.*21_*47del, NM_001289190.2:c.*22_*47del, NM_001289190.2:c.*23_*47del, NM_001289190.2:c.*24_*47del, NM_001289190.2:c.*25_*47del, NM_001289190.2:c.*26_*47del, NM_001289190.2:c.*27_*47del, NM_001289190.2:c.*28_*47del, NM_001289190.2:c.*29_*47del, NM_001289190.2:c.*30_*47del, NM_001289190.2:c.*31_*47del, NM_001289190.2:c.*32_*47del, NM_001289190.2:c.*33_*47del, NM_001289190.2:c.*34_*47del, NM_001289190.2:c.*35_*47del, NM_001289190.2:c.*36_*47del, NM_001289190.2:c.*37_*47del, NM_001289190.2:c.*38_*47del, NM_001289190.2:c.*40_*47del, NM_001289190.2:c.*41_*47del, NM_001289190.2:c.*42_*47del, NM_001289190.2:c.*47del, NM_001289190.2:c.*47dup, NM_001289190.2:c.*43_*47dup, NM_001289190.2:c.*41_*47dup, NM_001289190.2:c.*37_*47dup, NM_001289190.2:c.*36_*47dup, NM_001289190.1:c.*8_*47del, NM_001289190.1:c.*10_*47del, NM_001289190.1:c.*11_*47del, NM_001289190.1:c.*12_*47del, NM_001289190.1:c.*13_*47del, NM_001289190.1:c.*14_*47del, NM_001289190.1:c.*15_*47del, NM_001289190.1:c.*16_*47del, NM_001289190.1:c.*17_*47del, NM_001289190.1:c.*18_*47del, NM_001289190.1:c.*19_*47del, NM_001289190.1:c.*20_*47del, NM_001289190.1:c.*21_*47del, NM_001289190.1:c.*22_*47del, NM_001289190.1:c.*23_*47del, NM_001289190.1:c.*24_*47del, NM_001289190.1:c.*25_*47del, NM_001289190.1:c.*26_*47del, NM_001289190.1:c.*27_*47del, NM_001289190.1:c.*28_*47del, NM_001289190.1:c.*29_*47del, NM_001289190.1:c.*30_*47del, NM_001289190.1:c.*31_*47del, NM_001289190.1:c.*32_*47del, NM_001289190.1:c.*33_*47del, NM_001289190.1:c.*34_*47del, NM_001289190.1:c.*35_*47del, NM_001289190.1:c.*36_*47del, NM_001289190.1:c.*37_*47del, NM_001289190.1:c.*38_*47del, NM_001289190.1:c.*40_*47del, NM_001289190.1:c.*41_*47del, NM_001289190.1:c.*42_*47del, NM_001289190.1:c.*47del, NM_001289190.1:c.*47dup, NM_001289190.1:c.*43_*47dup, NM_001289190.1:c.*41_*47dup, NM_001289190.1:c.*37_*47dup, NM_001289190.1:c.*36_*47dup, XM_011527111.4:c.*8_*47del, XM_011527111.4:c.*10_*47del, XM_011527111.4:c.*11_*47del, XM_011527111.4:c.*12_*47del, XM_011527111.4:c.*13_*47del, XM_011527111.4:c.*14_*47del, XM_011527111.4:c.*15_*47del, XM_011527111.4:c.*16_*47del, XM_011527111.4:c.*17_*47del, XM_011527111.4:c.*18_*47del, XM_011527111.4:c.*19_*47del, XM_011527111.4:c.*20_*47del, XM_011527111.4:c.*21_*47del, XM_011527111.4:c.*22_*47del, XM_011527111.4:c.*23_*47del, XM_011527111.4:c.*24_*47del, XM_011527111.4:c.*25_*47del, XM_011527111.4:c.*26_*47del, XM_011527111.4:c.*27_*47del, XM_011527111.4:c.*28_*47del, XM_011527111.4:c.*29_*47del, XM_011527111.4:c.*30_*47del, XM_011527111.4:c.*31_*47del, XM_011527111.4:c.*32_*47del, XM_011527111.4:c.*33_*47del, XM_011527111.4:c.*34_*47del, XM_011527111.4:c.*35_*47del, XM_011527111.4:c.*36_*47del, XM_011527111.4:c.*37_*47del, XM_011527111.4:c.*38_*47del, XM_011527111.4:c.*40_*47del, XM_011527111.4:c.*41_*47del, XM_011527111.4:c.*42_*47del, XM_011527111.4:c.*47del, XM_011527111.4:c.*47dup, XM_011527111.4:c.*43_*47dup, XM_011527111.4:c.*41_*47dup, XM_011527111.4:c.*37_*47dup, XM_011527111.4:c.*36_*47dup, XM_011527111.3:c.*8_*47del, XM_011527111.3:c.*10_*47del, XM_011527111.3:c.*11_*47del, XM_011527111.3:c.*12_*47del, XM_011527111.3:c.*13_*47del, XM_011527111.3:c.*14_*47del, XM_011527111.3:c.*15_*47del, XM_011527111.3:c.*16_*47del, XM_011527111.3:c.*17_*47del, XM_011527111.3:c.*18_*47del, XM_011527111.3:c.*19_*47del, XM_011527111.3:c.*20_*47del, XM_011527111.3:c.*21_*47del, XM_011527111.3:c.*22_*47del, XM_011527111.3:c.*23_*47del, XM_011527111.3:c.*24_*47del, XM_011527111.3:c.*25_*47del, XM_011527111.3:c.*26_*47del, XM_011527111.3:c.*27_*47del, XM_011527111.3:c.*28_*47del, XM_011527111.3:c.*29_*47del, XM_011527111.3:c.*30_*47del, XM_011527111.3:c.*31_*47del, XM_011527111.3:c.*32_*47del, XM_011527111.3:c.*33_*47del, XM_011527111.3:c.*34_*47del, XM_011527111.3:c.*35_*47del, XM_011527111.3:c.*36_*47del, XM_011527111.3:c.*37_*47del, XM_011527111.3:c.*38_*47del, XM_011527111.3:c.*40_*47del, XM_011527111.3:c.*41_*47del, XM_011527111.3:c.*42_*47del, XM_011527111.3:c.*47del, XM_011527111.3:c.*47dup, XM_011527111.3:c.*43_*47dup, XM_011527111.3:c.*41_*47dup, XM_011527111.3:c.*37_*47dup, XM_011527111.3:c.*36_*47dup, XM_011527111.2:c.*8_*47del, XM_011527111.2:c.*10_*47del, XM_011527111.2:c.*11_*47del, XM_011527111.2:c.*12_*47del, XM_011527111.2:c.*13_*47del, XM_011527111.2:c.*14_*47del, XM_011527111.2:c.*15_*47del, XM_011527111.2:c.*16_*47del, XM_011527111.2:c.*17_*47del, XM_011527111.2:c.*18_*47del, XM_011527111.2:c.*19_*47del, XM_011527111.2:c.*20_*47del, XM_011527111.2:c.*21_*47del, XM_011527111.2:c.*22_*47del, XM_011527111.2:c.*23_*47del, XM_011527111.2:c.*24_*47del, XM_011527111.2:c.*25_*47del, XM_011527111.2:c.*26_*47del, XM_011527111.2:c.*27_*47del, XM_011527111.2:c.*28_*47del, XM_011527111.2:c.*29_*47del, XM_011527111.2:c.*30_*47del, XM_011527111.2:c.*31_*47del, XM_011527111.2:c.*32_*47del, XM_011527111.2:c.*33_*47del, XM_011527111.2:c.*34_*47del, XM_011527111.2:c.*35_*47del, XM_011527111.2:c.*36_*47del, XM_011527111.2:c.*37_*47del, XM_011527111.2:c.*38_*47del, XM_011527111.2:c.*40_*47del, XM_011527111.2:c.*41_*47del, XM_011527111.2:c.*42_*47del, XM_011527111.2:c.*47del, XM_011527111.2:c.*47dup, XM_011527111.2:c.*43_*47dup, XM_011527111.2:c.*41_*47dup, XM_011527111.2:c.*37_*47dup, XM_011527111.2:c.*36_*47dup, XM_011527111.1:c.*8_*47del, XM_011527111.1:c.*10_*47del, XM_011527111.1:c.*11_*47del, XM_011527111.1:c.*12_*47del, XM_011527111.1:c.*13_*47del, XM_011527111.1:c.*14_*47del, XM_011527111.1:c.*15_*47del, XM_011527111.1:c.*16_*47del, XM_011527111.1:c.*17_*47del, XM_011527111.1:c.*18_*47del, XM_011527111.1:c.*19_*47del, XM_011527111.1:c.*20_*47del, XM_011527111.1:c.*21_*47del, XM_011527111.1:c.*22_*47del, XM_011527111.1:c.*23_*47del, XM_011527111.1:c.*24_*47del, XM_011527111.1:c.*25_*47del, XM_011527111.1:c.*26_*47del, XM_011527111.1:c.*27_*47del, XM_011527111.1:c.*28_*47del, XM_011527111.1:c.*29_*47del, XM_011527111.1:c.*30_*47del, XM_011527111.1:c.*31_*47del, XM_011527111.1:c.*32_*47del, XM_011527111.1:c.*33_*47del, XM_011527111.1:c.*34_*47del, XM_011527111.1:c.*35_*47del, XM_011527111.1:c.*36_*47del, XM_011527111.1:c.*37_*47del, XM_011527111.1:c.*38_*47del, XM_011527111.1:c.*40_*47del, XM_011527111.1:c.*41_*47del, XM_011527111.1:c.*42_*47del, XM_011527111.1:c.*47del, XM_011527111.1:c.*47dup, XM_011527111.1:c.*43_*47dup, XM_011527111.1:c.*41_*47dup, XM_011527111.1:c.*37_*47dup, XM_011527111.1:c.*36_*47dup, XM_024451607.2:c.*8_*47del, XM_024451607.2:c.*10_*47del, XM_024451607.2:c.*11_*47del, XM_024451607.2:c.*12_*47del, XM_024451607.2:c.*13_*47del, XM_024451607.2:c.*14_*47del, XM_024451607.2:c.*15_*47del, XM_024451607.2:c.*16_*47del, XM_024451607.2:c.*17_*47del, XM_024451607.2:c.*18_*47del, XM_024451607.2:c.*19_*47del, XM_024451607.2:c.*20_*47del, XM_024451607.2:c.*21_*47del, XM_024451607.2:c.*22_*47del, XM_024451607.2:c.*23_*47del, XM_024451607.2:c.*24_*47del, XM_024451607.2:c.*25_*47del, XM_024451607.2:c.*26_*47del, XM_024451607.2:c.*27_*47del, XM_024451607.2:c.*28_*47del, XM_024451607.2:c.*29_*47del, XM_024451607.2:c.*30_*47del, XM_024451607.2:c.*31_*47del, XM_024451607.2:c.*32_*47del, XM_024451607.2:c.*33_*47del, XM_024451607.2:c.*34_*47del, XM_024451607.2:c.*35_*47del, XM_024451607.2:c.*36_*47del, XM_024451607.2:c.*37_*47del, XM_024451607.2:c.*38_*47del, XM_024451607.2:c.*40_*47del, XM_024451607.2:c.*41_*47del, XM_024451607.2:c.*42_*47del, XM_024451607.2:c.*47del, XM_024451607.2:c.*47dup, XM_024451607.2:c.*43_*47dup, XM_024451607.2:c.*41_*47dup, XM_024451607.2:c.*37_*47dup, XM_024451607.2:c.*36_*47dup, XM_024451607.1:c.*8_*47del, XM_024451607.1:c.*10_*47del, XM_024451607.1:c.*11_*47del, XM_024451607.1:c.*12_*47del, XM_024451607.1:c.*13_*47del, XM_024451607.1:c.*14_*47del, XM_024451607.1:c.*15_*47del, XM_024451607.1:c.*16_*47del, XM_024451607.1:c.*17_*47del, XM_024451607.1:c.*18_*47del, XM_024451607.1:c.*19_*47del, XM_024451607.1:c.*20_*47del, XM_024451607.1:c.*21_*47del, XM_024451607.1:c.*22_*47del, XM_024451607.1:c.*23_*47del, XM_024451607.1:c.*24_*47del, XM_024451607.1:c.*25_*47del, XM_024451607.1:c.*26_*47del, XM_024451607.1:c.*27_*47del, XM_024451607.1:c.*28_*47del, XM_024451607.1:c.*29_*47del, XM_024451607.1:c.*30_*47del, XM_024451607.1:c.*31_*47del, XM_024451607.1:c.*32_*47del, XM_024451607.1:c.*33_*47del, XM_024451607.1:c.*34_*47del, XM_024451607.1:c.*35_*47del, XM_024451607.1:c.*36_*47del, XM_024451607.1:c.*37_*47del, XM_024451607.1:c.*38_*47del, XM_024451607.1:c.*40_*47del, XM_024451607.1:c.*41_*47del, XM_024451607.1:c.*42_*47del, XM_024451607.1:c.*47del, XM_024451607.1:c.*47dup, XM_024451607.1:c.*43_*47dup, XM_024451607.1:c.*41_*47dup, XM_024451607.1:c.*37_*47dup, XM_024451607.1:c.*36_*47dup, XM_017026986.2:c.*8_*47del, XM_017026986.2:c.*10_*47del, XM_017026986.2:c.*11_*47del, XM_017026986.2:c.*12_*47del, XM_017026986.2:c.*13_*47del, XM_017026986.2:c.*14_*47del, XM_017026986.2:c.*15_*47del, XM_017026986.2:c.*16_*47del, XM_017026986.2:c.*17_*47del, XM_017026986.2:c.*18_*47del, XM_017026986.2:c.*19_*47del, XM_017026986.2:c.*20_*47del, XM_017026986.2:c.*21_*47del, XM_017026986.2:c.*22_*47del, XM_017026986.2:c.*23_*47del, XM_017026986.2:c.*24_*47del, XM_017026986.2:c.*25_*47del, XM_017026986.2:c.*26_*47del, XM_017026986.2:c.*27_*47del, XM_017026986.2:c.*28_*47del, XM_017026986.2:c.*29_*47del, XM_017026986.2:c.*30_*47del, XM_017026986.2:c.*31_*47del, XM_017026986.2:c.*32_*47del, XM_017026986.2:c.*33_*47del, XM_017026986.2:c.*34_*47del, XM_017026986.2:c.*35_*47del, XM_017026986.2:c.*36_*47del, XM_017026986.2:c.*37_*47del, XM_017026986.2:c.*38_*47del, XM_017026986.2:c.*40_*47del, XM_017026986.2:c.*41_*47del, XM_017026986.2:c.*42_*47del, XM_017026986.2:c.*47del, XM_017026986.2:c.*47dup, XM_017026986.2:c.*43_*47dup, XM_017026986.2:c.*41_*47dup, XM_017026986.2:c.*37_*47dup, XM_017026986.2:c.*36_*47dup, XM_017026986.1:c.*8_*47del, XM_017026986.1:c.*10_*47del, XM_017026986.1:c.*11_*47del, XM_017026986.1:c.*12_*47del, XM_017026986.1:c.*13_*47del, XM_017026986.1:c.*14_*47del, XM_017026986.1:c.*15_*47del, XM_017026986.1:c.*16_*47del, XM_017026986.1:c.*17_*47del, XM_017026986.1:c.*18_*47del, XM_017026986.1:c.*19_*47del, XM_017026986.1:c.*20_*47del, XM_017026986.1:c.*21_*47del, XM_017026986.1:c.*22_*47del, XM_017026986.1:c.*23_*47del, XM_017026986.1:c.*24_*47del, XM_017026986.1:c.*25_*47del, XM_017026986.1:c.*26_*47del, XM_017026986.1:c.*27_*47del, XM_017026986.1:c.*28_*47del, XM_017026986.1:c.*29_*47del, XM_017026986.1:c.*30_*47del, XM_017026986.1:c.*31_*47del, XM_017026986.1:c.*32_*47del, XM_017026986.1:c.*33_*47del, XM_017026986.1:c.*34_*47del, XM_017026986.1:c.*35_*47del, XM_017026986.1:c.*36_*47del, XM_017026986.1:c.*37_*47del, XM_017026986.1:c.*38_*47del, XM_017026986.1:c.*40_*47del, XM_017026986.1:c.*41_*47del, XM_017026986.1:c.*42_*47del, XM_017026986.1:c.*47del, XM_017026986.1:c.*47dup, XM_017026986.1:c.*43_*47dup, XM_017026986.1:c.*41_*47dup, XM_017026986.1:c.*37_*47dup, XM_017026986.1:c.*36_*47dup, XM_024451606.2:c.*8_*47del, XM_024451606.2:c.*10_*47del, XM_024451606.2:c.*11_*47del, XM_024451606.2:c.*12_*47del, XM_024451606.2:c.*13_*47del, XM_024451606.2:c.*14_*47del, XM_024451606.2:c.*15_*47del, XM_024451606.2:c.*16_*47del, XM_024451606.2:c.*17_*47del, XM_024451606.2:c.*18_*47del, XM_024451606.2:c.*19_*47del, XM_024451606.2:c.*20_*47del, XM_024451606.2:c.*21_*47del, XM_024451606.2:c.*22_*47del, XM_024451606.2:c.*23_*47del, XM_024451606.2:c.*24_*47del, XM_024451606.2:c.*25_*47del, XM_024451606.2:c.*26_*47del, XM_024451606.2:c.*27_*47del, XM_024451606.2:c.*28_*47del, XM_024451606.2:c.*29_*47del, XM_024451606.2:c.*30_*47del, XM_024451606.2:c.*31_*47del, XM_024451606.2:c.*32_*47del, XM_024451606.2:c.*33_*47del, XM_024451606.2:c.*34_*47del, XM_024451606.2:c.*35_*47del, XM_024451606.2:c.*36_*47del, XM_024451606.2:c.*37_*47del, XM_024451606.2:c.*38_*47del, XM_024451606.2:c.*40_*47del, XM_024451606.2:c.*41_*47del, XM_024451606.2:c.*42_*47del, XM_024451606.2:c.*47del, XM_024451606.2:c.*47dup, XM_024451606.2:c.*43_*47dup, XM_024451606.2:c.*41_*47dup, XM_024451606.2:c.*37_*47dup, XM_024451606.2:c.*36_*47dup, XM_024451606.1:c.*8_*47del, XM_024451606.1:c.*10_*47del, XM_024451606.1:c.*11_*47del, XM_024451606.1:c.*12_*47del, XM_024451606.1:c.*13_*47del, XM_024451606.1:c.*14_*47del, XM_024451606.1:c.*15_*47del, XM_024451606.1:c.*16_*47del, XM_024451606.1:c.*17_*47del, XM_024451606.1:c.*18_*47del, XM_024451606.1:c.*19_*47del, XM_024451606.1:c.*20_*47del, XM_024451606.1:c.*21_*47del, XM_024451606.1:c.*22_*47del, XM_024451606.1:c.*23_*47del, XM_024451606.1:c.*24_*47del, XM_024451606.1:c.*25_*47del, XM_024451606.1:c.*26_*47del, XM_024451606.1:c.*27_*47del, XM_024451606.1:c.*28_*47del, XM_024451606.1:c.*29_*47del, XM_024451606.1:c.*30_*47del, XM_024451606.1:c.*31_*47del, XM_024451606.1:c.*32_*47del, XM_024451606.1:c.*33_*47del, XM_024451606.1:c.*34_*47del, XM_024451606.1:c.*35_*47del, XM_024451606.1:c.*36_*47del, XM_024451606.1:c.*37_*47del, XM_024451606.1:c.*38_*47del, XM_024451606.1:c.*40_*47del, XM_024451606.1:c.*41_*47del, XM_024451606.1:c.*42_*47del, XM_024451606.1:c.*47del, XM_024451606.1:c.*47dup, XM_024451606.1:c.*43_*47dup, XM_024451606.1:c.*41_*47dup, XM_024451606.1:c.*37_*47dup, XM_024451606.1:c.*36_*47dup, XM_017026983.2:c.*8_*47del, XM_017026983.2:c.*10_*47del, XM_017026983.2:c.*11_*47del, XM_017026983.2:c.*12_*47del, XM_017026983.2:c.*13_*47del, XM_017026983.2:c.*14_*47del, XM_017026983.2:c.*15_*47del, XM_017026983.2:c.*16_*47del, XM_017026983.2:c.*17_*47del, XM_017026983.2:c.*18_*47del, XM_017026983.2:c.*19_*47del, XM_017026983.2:c.*20_*47del, XM_017026983.2:c.*21_*47del, XM_017026983.2:c.*22_*47del, XM_017026983.2:c.*23_*47del, XM_017026983.2:c.*24_*47del, XM_017026983.2:c.*25_*47del, XM_017026983.2:c.*26_*47del, XM_017026983.2:c.*27_*47del, XM_017026983.2:c.*28_*47del, XM_017026983.2:c.*29_*47del, XM_017026983.2:c.*30_*47del, XM_017026983.2:c.*31_*47del, XM_017026983.2:c.*32_*47del, XM_017026983.2:c.*33_*47del, XM_017026983.2:c.*34_*47del, XM_017026983.2:c.*35_*47del, XM_017026983.2:c.*36_*47del, XM_017026983.2:c.*37_*47del, XM_017026983.2:c.*38_*47del, XM_017026983.2:c.*40_*47del, XM_017026983.2:c.*41_*47del, XM_017026983.2:c.*42_*47del, XM_017026983.2:c.*47del, XM_017026983.2:c.*47dup, XM_017026983.2:c.*43_*47dup, XM_017026983.2:c.*41_*47dup, XM_017026983.2:c.*37_*47dup, XM_017026983.2:c.*36_*47dup, XM_017026983.1:c.*8_*47del, XM_017026983.1:c.*10_*47del, XM_017026983.1:c.*11_*47del, XM_017026983.1:c.*12_*47del, XM_017026983.1:c.*13_*47del, XM_017026983.1:c.*14_*47del, XM_017026983.1:c.*15_*47del, XM_017026983.1:c.*16_*47del, XM_017026983.1:c.*17_*47del, XM_017026983.1:c.*18_*47del, XM_017026983.1:c.*19_*47del, XM_017026983.1:c.*20_*47del, XM_017026983.1:c.*21_*47del, XM_017026983.1:c.*22_*47del, XM_017026983.1:c.*23_*47del, XM_017026983.1:c.*24_*47del, XM_017026983.1:c.*25_*47del, XM_017026983.1:c.*26_*47del, XM_017026983.1:c.*27_*47del, XM_017026983.1:c.*28_*47del, XM_017026983.1:c.*29_*47del, XM_017026983.1:c.*30_*47del, XM_017026983.1:c.*31_*47del, XM_017026983.1:c.*32_*47del, XM_017026983.1:c.*33_*47del, XM_017026983.1:c.*34_*47del, XM_017026983.1:c.*35_*47del, XM_017026983.1:c.*36_*47del, XM_017026983.1:c.*37_*47del, XM_017026983.1:c.*38_*47del, XM_017026983.1:c.*40_*47del, XM_017026983.1:c.*41_*47del, XM_017026983.1:c.*42_*47del, XM_017026983.1:c.*47del, XM_017026983.1:c.*47dup, XM_017026983.1:c.*43_*47dup, XM_017026983.1:c.*41_*47dup, XM_017026983.1:c.*37_*47dup, XM_017026983.1:c.*36_*47dup, XM_017026985.2:c.*8_*47del, XM_017026985.2:c.*10_*47del, XM_017026985.2:c.*11_*47del, XM_017026985.2:c.*12_*47del, XM_017026985.2:c.*13_*47del, XM_017026985.2:c.*14_*47del, XM_017026985.2:c.*15_*47del, XM_017026985.2:c.*16_*47del, XM_017026985.2:c.*17_*47del, XM_017026985.2:c.*18_*47del, XM_017026985.2:c.*19_*47del, XM_017026985.2:c.*20_*47del, XM_017026985.2:c.*21_*47del, XM_017026985.2:c.*22_*47del, XM_017026985.2:c.*23_*47del, XM_017026985.2:c.*24_*47del, XM_017026985.2:c.*25_*47del, XM_017026985.2:c.*26_*47del, XM_017026985.2:c.*27_*47del, XM_017026985.2:c.*28_*47del, XM_017026985.2:c.*29_*47del, XM_017026985.2:c.*30_*47del, XM_017026985.2:c.*31_*47del, XM_017026985.2:c.*32_*47del, XM_017026985.2:c.*33_*47del, XM_017026985.2:c.*34_*47del, XM_017026985.2:c.*35_*47del, XM_017026985.2:c.*36_*47del, XM_017026985.2:c.*37_*47del, XM_017026985.2:c.*38_*47del, XM_017026985.2:c.*40_*47del, XM_017026985.2:c.*41_*47del, XM_017026985.2:c.*42_*47del, XM_017026985.2:c.*47del, XM_017026985.2:c.*47dup, XM_017026985.2:c.*43_*47dup, XM_017026985.2:c.*41_*47dup, XM_017026985.2:c.*37_*47dup, XM_017026985.2:c.*36_*47dup, XM_017026985.1:c.*8_*47del, XM_017026985.1:c.*10_*47del, XM_017026985.1:c.*11_*47del, XM_017026985.1:c.*12_*47del, XM_017026985.1:c.*13_*47del, XM_017026985.1:c.*14_*47del, XM_017026985.1:c.*15_*47del, XM_017026985.1:c.*16_*47del, XM_017026985.1:c.*17_*47del, XM_017026985.1:c.*18_*47del, XM_017026985.1:c.*19_*47del, XM_017026985.1:c.*20_*47del, XM_017026985.1:c.*21_*47del, XM_017026985.1:c.*22_*47del, XM_017026985.1:c.*23_*47del, XM_017026985.1:c.*24_*47del, XM_017026985.1:c.*25_*47del, XM_017026985.1:c.*26_*47del, XM_017026985.1:c.*27_*47del, XM_017026985.1:c.*28_*47del, XM_017026985.1:c.*29_*47del, XM_017026985.1:c.*30_*47del, XM_017026985.1:c.*31_*47del, XM_017026985.1:c.*32_*47del, XM_017026985.1:c.*33_*47del, XM_017026985.1:c.*34_*47del, XM_017026985.1:c.*35_*47del, XM_017026985.1:c.*36_*47del, XM_017026985.1:c.*37_*47del, XM_017026985.1:c.*38_*47del, XM_017026985.1:c.*40_*47del, XM_017026985.1:c.*41_*47del, XM_017026985.1:c.*42_*47del, XM_017026985.1:c.*47del, XM_017026985.1:c.*47dup, XM_017026985.1:c.*43_*47dup, XM_017026985.1:c.*41_*47dup, XM_017026985.1:c.*37_*47dup, XM_017026985.1:c.*36_*47dup

                            14.

                            rs1488707846 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              A>C [Show Flanks]
                              Chromosome:
                              19:34676769 (GRCh38)
                              19:35167674 (GRCh37)
                              Canonical SPDI:
                              NC_000019.10:34676768:A:C
                              Gene:
                              ZNF302 (Varview), SCGB2B2 (Varview), SCGB1B2P (Varview), ZNF807P (Varview)
                              Functional Consequence:
                              non_coding_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,genic_upstream_transcript_variant
                              Validated:
                              by frequency
                              MAF:
                              C=0.000007/1 (GnomAD)
                              HGVS:

                              15.

                              rs1488676760 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                19:34674498 (GRCh38)
                                19:35165403 (GRCh37)
                                Canonical SPDI:
                                NC_000019.10:34674497:C:T
                                Gene:
                                ZNF302 (Varview), SCGB2B2 (Varview), SCGB1B2P (Varview), ZNF807P (Varview)
                                Functional Consequence:
                                2KB_upstream_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000021/3 (GnomAD)
                                T=0.00003/8 (TOPMED)
                                HGVS:

                                16.

                                rs1488594242 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>C [Show Flanks]
                                  Chromosome:
                                  19:34680714 (GRCh38)
                                  19:35171619 (GRCh37)
                                  Canonical SPDI:
                                  NC_000019.10:34680713:G:C
                                  Gene:
                                  ZNF302 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  C=0./0 (ALFA)
                                  C=0.000004/1 (TOPMED)
                                  HGVS:

                                  17.

                                  rs1488532935 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    GT>- [Show Flanks]
                                    Chromosome:
                                    19:34686774 (GRCh38)
                                    19:35177679 (GRCh37)
                                    Canonical SPDI:
                                    NC_000019.10:34686772:TGT:T
                                    Gene:
                                    ZNF302 (Varview)
                                    Functional Consequence:
                                    downstream_transcript_variant,500B_downstream_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    T=0./0 (ALFA)
                                    -=0.000004/1 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1488519717 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      19:34682774 (GRCh38)
                                      19:35173679 (GRCh37)
                                      Canonical SPDI:
                                      NC_000019.10:34682773:C:T
                                      Gene:
                                      ZNF302 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0./0 (ALFA)
                                      T=0.000008/2 (GnomAD_exomes)
                                      T=0.000008/2 (TOPMED)
                                      HGVS:

                                      19.

                                      rs1488024239 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>A,C [Show Flanks]
                                        Chromosome:
                                        19:34677678 (GRCh38)
                                        19:35168583 (GRCh37)
                                        Canonical SPDI:
                                        NC_000019.10:34677677:G:A,NC_000019.10:34677677:G:C
                                        Gene:
                                        ZNF302 (Varview), SCGB2B2 (Varview), SCGB1B2P (Varview), ZNF807P (Varview)
                                        Functional Consequence:
                                        2KB_upstream_variant,non_coding_transcript_variant,5_prime_UTR_variant,splice_donor_variant,upstream_transcript_variant,intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        C=0./0 (ALFA)
                                        A=0.000007/1 (GnomAD)
                                        C=0.000011/3 (TOPMED)
                                        HGVS:
                                        NC_000019.10:g.34677678G>A, NC_000019.10:g.34677678G>C, NC_000019.9:g.35168583G>A, NC_000019.9:g.35168583G>C, NG_033997.1:g.5040G>A, NG_033997.1:g.5040G>C, NM_018443.4:c.-247G>A, NM_018443.4:c.-247G>C, NM_018443.3:c.-247G>A, NM_018443.3:c.-247G>C, NM_018443.2:c.-247G>A, NM_018443.2:c.-247G>C, NM_018675.3:c.-494G>A, NM_018675.3:c.-494G>C, NM_018675.2:c.-494G>A, NM_018675.2:c.-494G>C, NM_001012320.3:c.-224G>A, NM_001012320.3:c.-224G>C, NM_001012320.2:c.-224G>A, NM_001012320.2:c.-224G>C, NM_001012320.1:c.-224G>A, NM_001012320.1:c.-224G>C, NM_001289188.2:c.-253G>A, NM_001289188.2:c.-253G>C, NM_001289188.1:c.-253G>A, NM_001289188.1:c.-253G>C, NM_001289189.2:c.-247G>A, NM_001289189.2:c.-247G>C, NM_001289189.1:c.-247G>A, NM_001289189.1:c.-247G>C, NM_001289192.2:c.-247G>A, NM_001289192.2:c.-247G>C, NM_001289192.1:c.-247G>A, NM_001289192.1:c.-247G>C, NM_001289182.2:c.-494G>A, NM_001289182.2:c.-494G>C, NM_001289182.1:c.-494G>A, NM_001289182.1:c.-494G>C, NM_001289187.2:c.-494G>A, NM_001289187.2:c.-494G>C, NM_001289187.1:c.-494G>A, NM_001289187.1:c.-494G>C, NM_001289191.2:c.-224G>A, NM_001289191.2:c.-224G>C, NM_001289191.1:c.-224G>A, NM_001289191.1:c.-224G>C, NM_001289190.2:c.-187G>A, NM_001289190.2:c.-187G>C, NM_001289190.1:c.-187G>A, NM_001289190.1:c.-187G>C, NM_001289181.2:c.-247G>A, NM_001289181.2:c.-247G>C, NM_001289181.1:c.-247G>A, NM_001289181.1:c.-247G>C, NM_001289184.2:c.-247G>A, NM_001289184.2:c.-247G>C, NM_001289184.1:c.-247G>A, NM_001289184.1:c.-247G>C, NM_001289185.2:c.-224G>A, NM_001289185.2:c.-224G>C, NM_001289185.1:c.-224G>A, NM_001289185.1:c.-224G>C, NM_001289183.2:c.-187G>A, NM_001289183.2:c.-187G>C, NM_001289183.1:c.-187G>A, NM_001289183.1:c.-187G>C, NM_001289186.2:c.-145G>A, NM_001289186.2:c.-145G>C, NM_001289186.1:c.-145G>A, NM_001289186.1:c.-145G>C, NR_110322.2:n.1G>A, NR_110322.2:n.1G>C, NR_110322.1:n.40G>A, NR_110322.1:n.40G>C, XM_011527111.4:c.-224G>A, XM_011527111.4:c.-224G>C, XM_011527111.2:c.-224G>A, XM_011527111.2:c.-224G>C, XM_017026980.3:c.-224G>A, XM_017026980.3:c.-224G>C, XM_017026981.3:c.-187G>A, XM_017026981.3:c.-187G>C, XM_024451607.2:c.-494G>A, XM_024451607.2:c.-494G>C, XM_024451607.1:c.-494G>A, XM_024451607.1:c.-494G>C, XM_017026986.2:c.-494G>A, XM_017026986.2:c.-494G>C, XM_017026986.1:c.-494G>A, XM_017026986.1:c.-494G>C, XM_024451606.2:c.-247G>A, XM_024451606.2:c.-247G>C, XM_024451606.1:c.-247G>A, XM_024451606.1:c.-247G>C, XM_017026978.2:c.-494G>A, XM_017026978.2:c.-494G>C, XM_017026978.1:c.-494G>A, XM_017026978.1:c.-494G>C, XM_017026979.2:c.-494G>A, XM_017026979.2:c.-494G>C, XM_017026979.1:c.-494G>A, XM_017026979.1:c.-494G>C, XM_017026983.2:c.-224G>A, XM_017026983.2:c.-224G>C, XM_017026983.1:c.-224G>A, XM_017026983.1:c.-224G>C, XM_017026985.2:c.-224G>A, XM_017026985.2:c.-224G>C, XM_017026985.1:c.-224G>A, XM_017026985.1:c.-224G>C, XM_024451603.2:c.-247G>A, XM_024451603.2:c.-247G>C, XM_024451603.1:c.-247G>A, XM_024451603.1:c.-247G>C, XM_017026982.2:c.-187G>A, XM_017026982.2:c.-187G>C

                                        20.

                                        rs1487950058 [Homo sapiens]
                                          Variant type:
                                          DEL
                                          Alleles:
                                          T>- [Show Flanks]
                                          Chromosome:
                                          19:34681791 (GRCh38)
                                          19:35172696 (GRCh37)
                                          Canonical SPDI:
                                          NC_000019.10:34681790:T:
                                          Gene:
                                          ZNF302 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          -=0./0 (ALFA)
                                          -=0.000004/1 (TOPMED)
                                          -=0.000007/1 (GnomAD)
                                          HGVS:

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