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Items: 1 to 20 of 544

1.

rs1490417810 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    7:99621555 (GRCh38)
    7:99219178 (GRCh37)
    Canonical SPDI:
    NC_000007.14:99621554:A:G
    Gene:
    ZSCAN25 (Varview)
    Functional Consequence:
    synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.0002/1 (ALFA)
    G=0.0002/1 (Estonian)
    HGVS:
    NC_000007.14:g.99621555A>G, NC_000007.13:g.99219178A>G, XM_011515909.3:c.570A>G, XM_011515909.2:c.570A>G, XM_011515909.1:c.570A>G, NM_145115.3:c.570A>G, NM_145115.2:c.570A>G, XM_011515905.3:c.570A>G, XM_011515905.2:c.570A>G, XM_011515905.1:c.570A>G, XM_011515907.3:c.570A>G, XM_011515907.2:c.570A>G, XM_011515907.1:c.570A>G, XR_927402.3:n.899A>G, XR_927402.2:n.1230A>G, XR_927402.1:n.1231A>G, XM_011515910.3:c.570A>G, XM_011515910.2:c.570A>G, XM_011515910.1:c.570A>G, NM_001350984.2:c.570A>G, NM_001350984.1:c.570A>G, NM_001350980.2:c.570A>G, NM_001350980.1:c.570A>G, NM_001350982.2:c.78A>G, NM_001350982.1:c.78A>G, NM_001350985.2:c.570A>G, NM_001350985.1:c.570A>G, NM_001350983.2:c.78A>G, NM_001350983.1:c.78A>G, NM_001350981.2:c.78A>G, NM_001350981.1:c.78A>G, NM_001350986.2:c.570A>G, NM_001350986.1:c.570A>G, NM_001350979.2:c.570A>G, NM_001350979.1:c.570A>G, XM_047420018.1:c.570A>G, XM_047420016.1:c.570A>G, XM_047420011.1:c.570A>G, XM_047420019.1:c.570A>G, XM_047420017.1:c.570A>G, XM_047420013.1:c.570A>G, XM_047420014.1:c.570A>G, XM_047420015.1:c.570A>G, XM_047420012.1:c.570A>G, XR_007059988.1:n.872A>G, XR_007059989.1:n.814A>G, XR_007059990.1:n.687A>G, XM_047420020.1:c.570A>G

    2.

    rs1482633949 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>T [Show Flanks]
      Chromosome:
      7:99629633 (GRCh38)
      7:99227256 (GRCh37)
      Canonical SPDI:
      NC_000007.14:99629632:C:T
      Gene:
      ZSCAN25 (Varview)
      Functional Consequence:
      3_prime_UTR_variant,intron_variant,coding_sequence_variant,synonymous_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0./0 (ALFA)
      T=0.000004/1 (TOPMED)
      T=0.000007/1 (GnomAD)
      HGVS:

      3.

      rs1482165734 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>T [Show Flanks]
        Chromosome:
        7:99621378 (GRCh38)
        7:99219001 (GRCh37)
        Canonical SPDI:
        NC_000007.14:99621377:A:T
        Gene:
        ZSCAN25 (Varview)
        Functional Consequence:
        non_coding_transcript_variant,5_prime_UTR_variant,coding_sequence_variant,synonymous_variant
        Validated:
        by frequency,by alfa
        MAF:
        T=0./0 (ALFA)
        T=0.000004/1 (TOPMED)
        HGVS:
        NC_000007.14:g.99621378A>T, NC_000007.13:g.99219001A>T, XM_011515909.3:c.393A>T, XM_011515909.2:c.393A>T, XM_011515909.1:c.393A>T, NM_145115.3:c.393A>T, NM_145115.2:c.393A>T, XM_011515905.3:c.393A>T, XM_011515905.2:c.393A>T, XM_011515905.1:c.393A>T, XM_011515907.3:c.393A>T, XM_011515907.2:c.393A>T, XM_011515907.1:c.393A>T, XR_927402.3:n.722A>T, XR_927402.2:n.1053A>T, XR_927402.1:n.1054A>T, XM_011515910.3:c.393A>T, XM_011515910.2:c.393A>T, XM_011515910.1:c.393A>T, NM_001350984.2:c.393A>T, NM_001350984.1:c.393A>T, NM_001350980.2:c.393A>T, NM_001350980.1:c.393A>T, NM_001350982.2:c.-100A>T, NM_001350982.1:c.-100A>T, NM_001350985.2:c.393A>T, NM_001350985.1:c.393A>T, NM_001350983.2:c.-100A>T, NM_001350983.1:c.-100A>T, NM_001350981.2:c.-100A>T, NM_001350981.1:c.-100A>T, NM_001350986.2:c.393A>T, NM_001350986.1:c.393A>T, NM_001350979.2:c.393A>T, NM_001350979.1:c.393A>T, XM_047420018.1:c.393A>T, XM_047420016.1:c.393A>T, XM_047420011.1:c.393A>T, XM_047420019.1:c.393A>T, XM_047420017.1:c.393A>T, XM_047420013.1:c.393A>T, XM_047420014.1:c.393A>T, XM_047420015.1:c.393A>T, XM_047420012.1:c.393A>T, XR_007059988.1:n.695A>T, XR_007059989.1:n.637A>T, XR_007059990.1:n.510A>T, XM_047420020.1:c.393A>T

        4.

        rs1481753808 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>T [Show Flanks]
          Chromosome:
          7:99621388 (GRCh38)
          7:99219011 (GRCh37)
          Canonical SPDI:
          NC_000007.14:99621387:C:T
          Gene:
          ZSCAN25 (Varview)
          Functional Consequence:
          non_coding_transcript_variant,stop_gained,5_prime_UTR_variant,coding_sequence_variant
          Validated:
          by frequency
          MAF:
          T=0.000006/1 (GnomAD_exomes)
          HGVS:
          NC_000007.14:g.99621388C>T, NC_000007.13:g.99219011C>T, XM_011515909.3:c.403C>T, XM_011515909.2:c.403C>T, XM_011515909.1:c.403C>T, NM_145115.3:c.403C>T, NM_145115.2:c.403C>T, XM_011515905.3:c.403C>T, XM_011515905.2:c.403C>T, XM_011515905.1:c.403C>T, XM_011515907.3:c.403C>T, XM_011515907.2:c.403C>T, XM_011515907.1:c.403C>T, XR_927402.3:n.732C>T, XR_927402.2:n.1063C>T, XR_927402.1:n.1064C>T, XM_011515910.3:c.403C>T, XM_011515910.2:c.403C>T, XM_011515910.1:c.403C>T, NM_001350984.2:c.403C>T, NM_001350984.1:c.403C>T, NM_001350980.2:c.403C>T, NM_001350980.1:c.403C>T, NM_001350982.2:c.-90C>T, NM_001350982.1:c.-90C>T, NM_001350985.2:c.403C>T, NM_001350985.1:c.403C>T, NM_001350983.2:c.-90C>T, NM_001350983.1:c.-90C>T, NM_001350981.2:c.-90C>T, NM_001350981.1:c.-90C>T, NM_001350986.2:c.403C>T, NM_001350986.1:c.403C>T, NM_001350979.2:c.403C>T, NM_001350979.1:c.403C>T, XM_047420018.1:c.403C>T, XM_047420016.1:c.403C>T, XM_047420011.1:c.403C>T, XM_047420019.1:c.403C>T, XM_047420017.1:c.403C>T, XM_047420013.1:c.403C>T, XM_047420014.1:c.403C>T, XM_047420015.1:c.403C>T, XM_047420012.1:c.403C>T, XR_007059988.1:n.705C>T, XR_007059989.1:n.647C>T, XR_007059990.1:n.520C>T, XM_047420020.1:c.403C>T, XP_011514211.1:p.Gln135Ter, NP_660090.2:p.Gln135Ter, XP_011514207.1:p.Gln135Ter, XP_011514209.1:p.Gln135Ter, XP_011514212.1:p.Gln135Ter, NP_001337913.1:p.Gln135Ter, NP_001337909.1:p.Gln135Ter, NP_001337914.1:p.Gln135Ter, NP_001337915.1:p.Gln135Ter, NP_001337908.1:p.Gln135Ter, XP_047275974.1:p.Gln135Ter, XP_047275972.1:p.Gln135Ter, XP_047275967.1:p.Gln135Ter, XP_047275975.1:p.Gln135Ter, XP_047275973.1:p.Gln135Ter, XP_047275969.1:p.Gln135Ter, XP_047275970.1:p.Gln135Ter, XP_047275971.1:p.Gln135Ter, XP_047275968.1:p.Gln135Ter, XP_047275976.1:p.Gln135Ter

          5.

          rs1480832572 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>A [Show Flanks]
            Chromosome:
            7:99621400 (GRCh38)
            7:99219023 (GRCh37)
            Canonical SPDI:
            NC_000007.14:99621399:G:A
            Gene:
            ZSCAN25 (Varview)
            Functional Consequence:
            non_coding_transcript_variant,missense_variant,5_prime_UTR_variant,coding_sequence_variant
            HGVS:
            NC_000007.14:g.99621400G>A, NC_000007.13:g.99219023G>A, XM_011515909.3:c.415G>A, XM_011515909.2:c.415G>A, XM_011515909.1:c.415G>A, NM_145115.3:c.415G>A, NM_145115.2:c.415G>A, XM_011515905.3:c.415G>A, XM_011515905.2:c.415G>A, XM_011515905.1:c.415G>A, XM_011515907.3:c.415G>A, XM_011515907.2:c.415G>A, XM_011515907.1:c.415G>A, XR_927402.3:n.744G>A, XR_927402.2:n.1075G>A, XR_927402.1:n.1076G>A, XM_011515910.3:c.415G>A, XM_011515910.2:c.415G>A, XM_011515910.1:c.415G>A, NM_001350984.2:c.415G>A, NM_001350984.1:c.415G>A, NM_001350980.2:c.415G>A, NM_001350980.1:c.415G>A, NM_001350982.2:c.-78G>A, NM_001350982.1:c.-78G>A, NM_001350985.2:c.415G>A, NM_001350985.1:c.415G>A, NM_001350983.2:c.-78G>A, NM_001350983.1:c.-78G>A, NM_001350981.2:c.-78G>A, NM_001350981.1:c.-78G>A, NM_001350986.2:c.415G>A, NM_001350986.1:c.415G>A, NM_001350979.2:c.415G>A, NM_001350979.1:c.415G>A, XM_047420018.1:c.415G>A, XM_047420016.1:c.415G>A, XM_047420011.1:c.415G>A, XM_047420019.1:c.415G>A, XM_047420017.1:c.415G>A, XM_047420013.1:c.415G>A, XM_047420014.1:c.415G>A, XM_047420015.1:c.415G>A, XM_047420012.1:c.415G>A, XR_007059988.1:n.717G>A, XR_007059989.1:n.659G>A, XR_007059990.1:n.532G>A, XM_047420020.1:c.415G>A, XP_011514211.1:p.Glu139Lys, NP_660090.2:p.Glu139Lys, XP_011514207.1:p.Glu139Lys, XP_011514209.1:p.Glu139Lys, XP_011514212.1:p.Glu139Lys, NP_001337913.1:p.Glu139Lys, NP_001337909.1:p.Glu139Lys, NP_001337914.1:p.Glu139Lys, NP_001337915.1:p.Glu139Lys, NP_001337908.1:p.Glu139Lys, XP_047275974.1:p.Glu139Lys, XP_047275972.1:p.Glu139Lys, XP_047275967.1:p.Glu139Lys, XP_047275975.1:p.Glu139Lys, XP_047275973.1:p.Glu139Lys, XP_047275969.1:p.Glu139Lys, XP_047275970.1:p.Glu139Lys, XP_047275971.1:p.Glu139Lys, XP_047275968.1:p.Glu139Lys, XP_047275976.1:p.Glu139Lys

            6.

            rs1480784546 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              7:99629335 (GRCh38)
              7:99226958 (GRCh37)
              Canonical SPDI:
              NC_000007.14:99629334:C:T
              Gene:
              ZSCAN25 (Varview)
              Functional Consequence:
              3_prime_UTR_variant,intron_variant,missense_variant,coding_sequence_variant
              HGVS:
              NC_000007.14:g.99629335C>T, NC_000007.13:g.99226958C>T, NM_145115.3:c.950C>T, NM_145115.2:c.950C>T, XM_011515905.3:c.950C>T, XM_011515905.2:c.950C>T, XM_011515905.1:c.950C>T, XM_011515907.3:c.950C>T, XM_011515907.2:c.950C>T, XM_011515907.1:c.950C>T, NM_001350980.2:c.950C>T, NM_001350980.1:c.950C>T, NM_001350982.2:c.458C>T, NM_001350982.1:c.458C>T, NM_001350983.2:c.458C>T, NM_001350983.1:c.458C>T, NM_001350981.2:c.458C>T, NM_001350981.1:c.458C>T, NM_001350986.2:c.*97C>T, NM_001350986.1:c.*97C>T, NM_001350979.2:c.950C>T, NM_001350979.1:c.950C>T, XM_047420011.1:c.950C>T, XM_047420013.1:c.950C>T, XM_047420014.1:c.950C>T, XM_047420015.1:c.950C>T, XM_047420012.1:c.950C>T, NP_660090.2:p.Pro317Leu, XP_011514207.1:p.Pro317Leu, XP_011514209.1:p.Pro317Leu, NP_001337909.1:p.Pro317Leu, NP_001337911.1:p.Pro153Leu, NP_001337912.1:p.Pro153Leu, NP_001337910.1:p.Pro153Leu, NP_001337908.1:p.Pro317Leu, XP_047275967.1:p.Pro317Leu, XP_047275969.1:p.Pro317Leu, XP_047275970.1:p.Pro317Leu, XP_047275971.1:p.Pro317Leu, XP_047275968.1:p.Pro317Leu

              7.

              rs1480016210 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                GAGGTTTCGGCAGTTCCGCT>- [Show Flanks]
                Chromosome:
                7:99619735 (GRCh38)
                7:99217358 (GRCh37)
                Canonical SPDI:
                NC_000007.14:99619731:GCTGAGGTTTCGGCAGTTCCGCT:GCT
                Gene:
                ZSCAN25 (Varview)
                Functional Consequence:
                non_coding_transcript_variant,frameshift_variant,5_prime_UTR_variant,coding_sequence_variant
                Validated:
                by frequency,by alfa
                MAF:
                GCT=0./0 (ALFA)
                -=0.000004/1 (TOPMED)
                HGVS:
                NC_000007.14:g.99619735_99619754del, NC_000007.13:g.99217358_99217377del, XM_011515909.3:c.129_148del, XM_011515909.2:c.129_148del, XM_011515909.1:c.129_148del, NM_145115.3:c.129_148del, NM_145115.2:c.129_148del, XM_011515905.3:c.129_148del, XM_011515905.2:c.129_148del, XM_011515905.1:c.129_148del, XM_011515907.3:c.129_148del, XM_011515907.2:c.129_148del, XM_011515907.1:c.129_148del, XR_927402.3:n.458_477del, XR_927402.2:n.789_808del, XR_927402.1:n.790_809del, XM_011515910.3:c.129_148del, XM_011515910.2:c.129_148del, XM_011515910.1:c.129_148del, NM_001350984.2:c.129_148del, NM_001350984.1:c.129_148del, NM_001350980.2:c.129_148del, NM_001350980.1:c.129_148del, NM_001350982.2:c.-368_-349del, NM_001350982.1:c.-368_-349del, NM_001350985.2:c.129_148del, NM_001350985.1:c.129_148del, NM_001350983.2:c.-368_-349del, NM_001350983.1:c.-368_-349del, NM_001350981.2:c.-368_-349del, NM_001350981.1:c.-368_-349del, NM_001350986.2:c.129_148del, NM_001350986.1:c.129_148del, NM_001350979.2:c.129_148del, NM_001350979.1:c.129_148del, XM_047420018.1:c.129_148del, XM_047420016.1:c.129_148del, XM_047420011.1:c.129_148del, XM_047420019.1:c.129_148del, XM_047420017.1:c.129_148del, XM_047420013.1:c.129_148del, XM_047420014.1:c.129_148del, XM_047420015.1:c.129_148del, XM_047420012.1:c.129_148del, XR_007059988.1:n.431_450del, XR_007059989.1:n.373_392del, XR_007059990.1:n.246_265del, XM_047420020.1:c.129_148del, XP_011514211.1:p.Arg44fs, NP_660090.2:p.Arg44fs, XP_011514207.1:p.Arg44fs, XP_011514209.1:p.Arg44fs, XP_011514212.1:p.Arg44fs, NP_001337913.1:p.Arg44fs, NP_001337909.1:p.Arg44fs, NP_001337914.1:p.Arg44fs, NP_001337915.1:p.Arg44fs, NP_001337908.1:p.Arg44fs, XP_047275974.1:p.Arg44fs, XP_047275972.1:p.Arg44fs, XP_047275967.1:p.Arg44fs, XP_047275975.1:p.Arg44fs, XP_047275973.1:p.Arg44fs, XP_047275969.1:p.Arg44fs, XP_047275970.1:p.Arg44fs, XP_047275971.1:p.Arg44fs, XP_047275968.1:p.Arg44fs, XP_047275976.1:p.Arg44fs

                8.

                rs1479799214 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>C [Show Flanks]
                  Chromosome:
                  7:99624144 (GRCh38)
                  7:99221767 (GRCh37)
                  Canonical SPDI:
                  NC_000007.14:99624143:G:C
                  Gene:
                  ZSCAN25 (Varview)
                  Functional Consequence:
                  non_coding_transcript_variant,intron_variant,missense_variant,coding_sequence_variant
                  Validated:
                  by frequency
                  MAF:
                  C=0.000004/1 (GnomAD_exomes)
                  HGVS:
                  NC_000007.14:g.99624144G>C, NC_000007.13:g.99221767G>C, XM_011515909.3:c.769G>C, XM_011515909.2:c.769G>C, XM_011515909.1:c.769G>C, NM_145115.3:c.769G>C, NM_145115.2:c.769G>C, XM_011515905.3:c.769G>C, XM_011515905.2:c.769G>C, XM_011515905.1:c.769G>C, XM_011515907.3:c.769G>C, XM_011515907.2:c.769G>C, XM_011515907.1:c.769G>C, XR_927402.3:n.1098G>C, XR_927402.2:n.1429G>C, XR_927402.1:n.1430G>C, XM_011515910.3:c.769G>C, XM_011515910.2:c.769G>C, XM_011515910.1:c.769G>C, NM_001350984.2:c.769G>C, NM_001350984.1:c.769G>C, NM_001350980.2:c.769G>C, NM_001350980.1:c.769G>C, NM_001350982.2:c.277G>C, NM_001350982.1:c.277G>C, NM_001350985.2:c.769G>C, NM_001350985.1:c.769G>C, NM_001350983.2:c.277G>C, NM_001350983.1:c.277G>C, NM_001350981.2:c.277G>C, NM_001350981.1:c.277G>C, NM_001350979.2:c.769G>C, NM_001350979.1:c.769G>C, XM_047420018.1:c.769G>C, XM_047420016.1:c.769G>C, XM_047420011.1:c.769G>C, XM_047420019.1:c.769G>C, XM_047420017.1:c.769G>C, XM_047420013.1:c.769G>C, XM_047420014.1:c.769G>C, XM_047420015.1:c.769G>C, XM_047420012.1:c.769G>C, XR_007059988.1:n.1071G>C, XR_007059989.1:n.1013G>C, XR_007059990.1:n.886G>C, XM_047420020.1:c.769G>C, XP_011514211.1:p.Glu257Gln, NP_660090.2:p.Glu257Gln, XP_011514207.1:p.Glu257Gln, XP_011514209.1:p.Glu257Gln, XP_011514212.1:p.Glu257Gln, NP_001337913.1:p.Glu257Gln, NP_001337909.1:p.Glu257Gln, NP_001337911.1:p.Glu93Gln, NP_001337914.1:p.Glu257Gln, NP_001337912.1:p.Glu93Gln, NP_001337910.1:p.Glu93Gln, NP_001337908.1:p.Glu257Gln, XP_047275974.1:p.Glu257Gln, XP_047275972.1:p.Glu257Gln, XP_047275967.1:p.Glu257Gln, XP_047275975.1:p.Glu257Gln, XP_047275973.1:p.Glu257Gln, XP_047275969.1:p.Glu257Gln, XP_047275970.1:p.Glu257Gln, XP_047275971.1:p.Glu257Gln, XP_047275968.1:p.Glu257Gln, XP_047275976.1:p.Glu257Gln

                  9.

                  rs1479666919 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>G [Show Flanks]
                    Chromosome:
                    7:99629812 (GRCh38)
                    7:99227435 (GRCh37)
                    Canonical SPDI:
                    NC_000007.14:99629811:A:G
                    Gene:
                    ZSCAN25 (Varview)
                    Functional Consequence:
                    3_prime_UTR_variant,intron_variant,missense_variant,coding_sequence_variant
                    Validated:
                    by frequency
                    MAF:
                    G=0.000004/1 (GnomAD_exomes)
                    HGVS:
                    NC_000007.14:g.99629812A>G, NC_000007.13:g.99227435A>G, NM_145115.3:c.1427A>G, NM_145115.2:c.1427A>G, XM_011515905.3:c.1427A>G, XM_011515905.2:c.1427A>G, XM_011515905.1:c.1427A>G, XM_011515907.3:c.1427A>G, XM_011515907.2:c.1427A>G, XM_011515907.1:c.1427A>G, NM_001350980.2:c.1427A>G, NM_001350980.1:c.1427A>G, NM_001350982.2:c.935A>G, NM_001350982.1:c.935A>G, NM_001350983.2:c.935A>G, NM_001350983.1:c.935A>G, NM_001350981.2:c.935A>G, NM_001350981.1:c.935A>G, NM_001350986.2:c.*574A>G, NM_001350986.1:c.*574A>G, NM_001350979.2:c.1427A>G, NM_001350979.1:c.1427A>G, XM_047420011.1:c.1427A>G, XM_047420013.1:c.1427A>G, XM_047420014.1:c.1427A>G, XM_047420015.1:c.1427A>G, XM_047420012.1:c.1427A>G, NP_660090.2:p.His476Arg, XP_011514207.1:p.His476Arg, XP_011514209.1:p.His476Arg, NP_001337909.1:p.His476Arg, NP_001337911.1:p.His312Arg, NP_001337912.1:p.His312Arg, NP_001337910.1:p.His312Arg, NP_001337908.1:p.His476Arg, XP_047275967.1:p.His476Arg, XP_047275969.1:p.His476Arg, XP_047275970.1:p.His476Arg, XP_047275971.1:p.His476Arg, XP_047275968.1:p.His476Arg

                    10.

                    rs1479130816 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A [Show Flanks]
                      Chromosome:
                      7:99619700 (GRCh38)
                      7:99217323 (GRCh37)
                      Canonical SPDI:
                      NC_000007.14:99619699:G:A
                      Gene:
                      ZSCAN25 (Varview)
                      Functional Consequence:
                      non_coding_transcript_variant,missense_variant,5_prime_UTR_variant,coding_sequence_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      A=0./0 (ALFA)
                      A=0.000015/4 (TOPMED)
                      HGVS:
                      NC_000007.14:g.99619700G>A, NC_000007.13:g.99217323G>A, XM_011515909.3:c.94G>A, XM_011515909.2:c.94G>A, XM_011515909.1:c.94G>A, NM_145115.3:c.94G>A, NM_145115.2:c.94G>A, XM_011515905.3:c.94G>A, XM_011515905.2:c.94G>A, XM_011515905.1:c.94G>A, XM_011515907.3:c.94G>A, XM_011515907.2:c.94G>A, XM_011515907.1:c.94G>A, XR_927402.3:n.423G>A, XR_927402.2:n.754G>A, XR_927402.1:n.755G>A, XM_011515910.3:c.94G>A, XM_011515910.2:c.94G>A, XM_011515910.1:c.94G>A, NM_001350984.2:c.94G>A, NM_001350984.1:c.94G>A, NM_001350980.2:c.94G>A, NM_001350980.1:c.94G>A, NM_001350982.2:c.-403G>A, NM_001350982.1:c.-403G>A, NM_001350985.2:c.94G>A, NM_001350985.1:c.94G>A, NM_001350983.2:c.-403G>A, NM_001350983.1:c.-403G>A, NM_001350981.2:c.-403G>A, NM_001350981.1:c.-403G>A, NM_001350986.2:c.94G>A, NM_001350986.1:c.94G>A, NM_001350979.2:c.94G>A, NM_001350979.1:c.94G>A, XM_047420018.1:c.94G>A, XM_047420016.1:c.94G>A, XM_047420011.1:c.94G>A, XM_047420019.1:c.94G>A, XM_047420017.1:c.94G>A, XM_047420013.1:c.94G>A, XM_047420014.1:c.94G>A, XM_047420015.1:c.94G>A, XM_047420012.1:c.94G>A, XR_007059988.1:n.396G>A, XR_007059989.1:n.338G>A, XR_007059990.1:n.211G>A, XM_047420020.1:c.94G>A, XP_011514211.1:p.Gly32Arg, NP_660090.2:p.Gly32Arg, XP_011514207.1:p.Gly32Arg, XP_011514209.1:p.Gly32Arg, XP_011514212.1:p.Gly32Arg, NP_001337913.1:p.Gly32Arg, NP_001337909.1:p.Gly32Arg, NP_001337914.1:p.Gly32Arg, NP_001337915.1:p.Gly32Arg, NP_001337908.1:p.Gly32Arg, XP_047275974.1:p.Gly32Arg, XP_047275972.1:p.Gly32Arg, XP_047275967.1:p.Gly32Arg, XP_047275975.1:p.Gly32Arg, XP_047275973.1:p.Gly32Arg, XP_047275969.1:p.Gly32Arg, XP_047275970.1:p.Gly32Arg, XP_047275971.1:p.Gly32Arg, XP_047275968.1:p.Gly32Arg, XP_047275976.1:p.Gly32Arg

                      11.

                      rs1477371727 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>A [Show Flanks]
                        Chromosome:
                        7:99619676 (GRCh38)
                        7:99217299 (GRCh37)
                        Canonical SPDI:
                        NC_000007.14:99619675:G:A
                        Gene:
                        ZSCAN25 (Varview)
                        Functional Consequence:
                        non_coding_transcript_variant,missense_variant,5_prime_UTR_variant,coding_sequence_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        A=0.000027/1 (ALFA)
                        A=0.000004/1 (GnomAD_exomes)
                        A=0.000007/1 (GnomAD)
                        A=0.000008/2 (TOPMED)
                        HGVS:
                        NC_000007.14:g.99619676G>A, NC_000007.13:g.99217299G>A, XM_011515909.3:c.70G>A, XM_011515909.2:c.70G>A, XM_011515909.1:c.70G>A, NM_145115.3:c.70G>A, NM_145115.2:c.70G>A, XM_011515905.3:c.70G>A, XM_011515905.2:c.70G>A, XM_011515905.1:c.70G>A, XM_011515907.3:c.70G>A, XM_011515907.2:c.70G>A, XM_011515907.1:c.70G>A, XR_927402.3:n.399G>A, XR_927402.2:n.730G>A, XR_927402.1:n.731G>A, XM_011515910.3:c.70G>A, XM_011515910.2:c.70G>A, XM_011515910.1:c.70G>A, NM_001350984.2:c.70G>A, NM_001350984.1:c.70G>A, NM_001350980.2:c.70G>A, NM_001350980.1:c.70G>A, NM_001350982.2:c.-427G>A, NM_001350982.1:c.-427G>A, NM_001350985.2:c.70G>A, NM_001350985.1:c.70G>A, NM_001350983.2:c.-427G>A, NM_001350983.1:c.-427G>A, NM_001350981.2:c.-427G>A, NM_001350981.1:c.-427G>A, NM_001350986.2:c.70G>A, NM_001350986.1:c.70G>A, NM_001350979.2:c.70G>A, NM_001350979.1:c.70G>A, XM_047420018.1:c.70G>A, XM_047420016.1:c.70G>A, XM_047420011.1:c.70G>A, XM_047420019.1:c.70G>A, XM_047420017.1:c.70G>A, XM_047420013.1:c.70G>A, XM_047420014.1:c.70G>A, XM_047420015.1:c.70G>A, XM_047420012.1:c.70G>A, XR_007059988.1:n.372G>A, XR_007059989.1:n.314G>A, XR_007059990.1:n.187G>A, XM_047420020.1:c.70G>A, XP_011514211.1:p.Glu24Lys, NP_660090.2:p.Glu24Lys, XP_011514207.1:p.Glu24Lys, XP_011514209.1:p.Glu24Lys, XP_011514212.1:p.Glu24Lys, NP_001337913.1:p.Glu24Lys, NP_001337909.1:p.Glu24Lys, NP_001337914.1:p.Glu24Lys, NP_001337915.1:p.Glu24Lys, NP_001337908.1:p.Glu24Lys, XP_047275974.1:p.Glu24Lys, XP_047275972.1:p.Glu24Lys, XP_047275967.1:p.Glu24Lys, XP_047275975.1:p.Glu24Lys, XP_047275973.1:p.Glu24Lys, XP_047275969.1:p.Glu24Lys, XP_047275970.1:p.Glu24Lys, XP_047275971.1:p.Glu24Lys, XP_047275968.1:p.Glu24Lys, XP_047275976.1:p.Glu24Lys

                        12.

                        rs1476583053 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A,C,T [Show Flanks]
                          Chromosome:
                          7:99619781 (GRCh38)
                          7:99217404 (GRCh37)
                          Canonical SPDI:
                          NC_000007.14:99619780:G:A,NC_000007.14:99619780:G:C,NC_000007.14:99619780:G:T
                          Gene:
                          ZSCAN25 (Varview)
                          Functional Consequence:
                          non_coding_transcript_variant,missense_variant,5_prime_UTR_variant,coding_sequence_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          T=0./0 (ALFA)
                          C=0.000004/1 (GnomAD_exomes)
                          A=0.000004/1 (TOPMED)
                          HGVS:
                          NC_000007.14:g.99619781G>A, NC_000007.14:g.99619781G>C, NC_000007.14:g.99619781G>T, NC_000007.13:g.99217404G>A, NC_000007.13:g.99217404G>C, NC_000007.13:g.99217404G>T, XM_011515909.3:c.175G>A, XM_011515909.3:c.175G>C, XM_011515909.3:c.175G>T, XM_011515909.2:c.175G>A, XM_011515909.2:c.175G>C, XM_011515909.2:c.175G>T, XM_011515909.1:c.175G>A, XM_011515909.1:c.175G>C, XM_011515909.1:c.175G>T, NM_145115.3:c.175G>A, NM_145115.3:c.175G>C, NM_145115.3:c.175G>T, NM_145115.2:c.175G>A, NM_145115.2:c.175G>C, NM_145115.2:c.175G>T, XM_011515905.3:c.175G>A, XM_011515905.3:c.175G>C, XM_011515905.3:c.175G>T, XM_011515905.2:c.175G>A, XM_011515905.2:c.175G>C, XM_011515905.2:c.175G>T, XM_011515905.1:c.175G>A, XM_011515905.1:c.175G>C, XM_011515905.1:c.175G>T, XM_011515907.3:c.175G>A, XM_011515907.3:c.175G>C, XM_011515907.3:c.175G>T, XM_011515907.2:c.175G>A, XM_011515907.2:c.175G>C, XM_011515907.2:c.175G>T, XM_011515907.1:c.175G>A, XM_011515907.1:c.175G>C, XM_011515907.1:c.175G>T, XR_927402.3:n.504G>A, XR_927402.3:n.504G>C, XR_927402.3:n.504G>T, XR_927402.2:n.835G>A, XR_927402.2:n.835G>C, XR_927402.2:n.835G>T, XR_927402.1:n.836G>A, XR_927402.1:n.836G>C, XR_927402.1:n.836G>T, XM_011515910.3:c.175G>A, XM_011515910.3:c.175G>C, XM_011515910.3:c.175G>T, XM_011515910.2:c.175G>A, XM_011515910.2:c.175G>C, XM_011515910.2:c.175G>T, XM_011515910.1:c.175G>A, XM_011515910.1:c.175G>C, XM_011515910.1:c.175G>T, NM_001350984.2:c.175G>A, NM_001350984.2:c.175G>C, NM_001350984.2:c.175G>T, NM_001350984.1:c.175G>A, NM_001350984.1:c.175G>C, NM_001350984.1:c.175G>T, NM_001350980.2:c.175G>A, NM_001350980.2:c.175G>C, NM_001350980.2:c.175G>T, NM_001350980.1:c.175G>A, NM_001350980.1:c.175G>C, NM_001350980.1:c.175G>T, NM_001350982.2:c.-322G>A, NM_001350982.2:c.-322G>C, NM_001350982.2:c.-322G>T, NM_001350982.1:c.-322G>A, NM_001350982.1:c.-322G>C, NM_001350982.1:c.-322G>T, NM_001350985.2:c.175G>A, NM_001350985.2:c.175G>C, NM_001350985.2:c.175G>T, NM_001350985.1:c.175G>A, NM_001350985.1:c.175G>C, NM_001350985.1:c.175G>T, NM_001350983.2:c.-322G>A, NM_001350983.2:c.-322G>C, NM_001350983.2:c.-322G>T, NM_001350983.1:c.-322G>A, NM_001350983.1:c.-322G>C, NM_001350983.1:c.-322G>T, NM_001350981.2:c.-322G>A, NM_001350981.2:c.-322G>C, NM_001350981.2:c.-322G>T, NM_001350981.1:c.-322G>A, NM_001350981.1:c.-322G>C, NM_001350981.1:c.-322G>T, NM_001350986.2:c.175G>A, NM_001350986.2:c.175G>C, NM_001350986.2:c.175G>T, NM_001350986.1:c.175G>A, NM_001350986.1:c.175G>C, NM_001350986.1:c.175G>T, NM_001350979.2:c.175G>A, NM_001350979.2:c.175G>C, NM_001350979.2:c.175G>T, NM_001350979.1:c.175G>A, NM_001350979.1:c.175G>C, NM_001350979.1:c.175G>T, XM_047420018.1:c.175G>A, XM_047420018.1:c.175G>C, XM_047420018.1:c.175G>T, XM_047420016.1:c.175G>A, XM_047420016.1:c.175G>C, XM_047420016.1:c.175G>T, XM_047420011.1:c.175G>A, XM_047420011.1:c.175G>C, XM_047420011.1:c.175G>T, XM_047420019.1:c.175G>A, XM_047420019.1:c.175G>C, XM_047420019.1:c.175G>T, XM_047420017.1:c.175G>A, XM_047420017.1:c.175G>C, XM_047420017.1:c.175G>T, XM_047420013.1:c.175G>A, XM_047420013.1:c.175G>C, XM_047420013.1:c.175G>T, XM_047420014.1:c.175G>A, XM_047420014.1:c.175G>C, XM_047420014.1:c.175G>T, XM_047420015.1:c.175G>A, XM_047420015.1:c.175G>C, XM_047420015.1:c.175G>T, XM_047420012.1:c.175G>A, XM_047420012.1:c.175G>C, XM_047420012.1:c.175G>T, XR_007059988.1:n.477G>A, XR_007059988.1:n.477G>C, XR_007059988.1:n.477G>T, XR_007059989.1:n.419G>A, XR_007059989.1:n.419G>C, XR_007059989.1:n.419G>T, XR_007059990.1:n.292G>A, XR_007059990.1:n.292G>C, XR_007059990.1:n.292G>T, XM_047420020.1:c.175G>A, XM_047420020.1:c.175G>C, XM_047420020.1:c.175G>T, XP_011514211.1:p.Ala59Thr, XP_011514211.1:p.Ala59Pro, XP_011514211.1:p.Ala59Ser, NP_660090.2:p.Ala59Thr, NP_660090.2:p.Ala59Pro, NP_660090.2:p.Ala59Ser, XP_011514207.1:p.Ala59Thr, XP_011514207.1:p.Ala59Pro, XP_011514207.1:p.Ala59Ser, XP_011514209.1:p.Ala59Thr, XP_011514209.1:p.Ala59Pro, XP_011514209.1:p.Ala59Ser, XP_011514212.1:p.Ala59Thr, XP_011514212.1:p.Ala59Pro, XP_011514212.1:p.Ala59Ser, NP_001337913.1:p.Ala59Thr, NP_001337913.1:p.Ala59Pro, NP_001337913.1:p.Ala59Ser, NP_001337909.1:p.Ala59Thr, NP_001337909.1:p.Ala59Pro, NP_001337909.1:p.Ala59Ser, NP_001337914.1:p.Ala59Thr, NP_001337914.1:p.Ala59Pro, NP_001337914.1:p.Ala59Ser, NP_001337915.1:p.Ala59Thr, NP_001337915.1:p.Ala59Pro, NP_001337915.1:p.Ala59Ser, NP_001337908.1:p.Ala59Thr, NP_001337908.1:p.Ala59Pro, NP_001337908.1:p.Ala59Ser, XP_047275974.1:p.Ala59Thr, XP_047275974.1:p.Ala59Pro, XP_047275974.1:p.Ala59Ser, XP_047275972.1:p.Ala59Thr, XP_047275972.1:p.Ala59Pro, XP_047275972.1:p.Ala59Ser, XP_047275967.1:p.Ala59Thr, XP_047275967.1:p.Ala59Pro, XP_047275967.1:p.Ala59Ser, XP_047275975.1:p.Ala59Thr, XP_047275975.1:p.Ala59Pro, XP_047275975.1:p.Ala59Ser, XP_047275973.1:p.Ala59Thr, XP_047275973.1:p.Ala59Pro, XP_047275973.1:p.Ala59Ser, XP_047275969.1:p.Ala59Thr, XP_047275969.1:p.Ala59Pro, XP_047275969.1:p.Ala59Ser, XP_047275970.1:p.Ala59Thr, XP_047275970.1:p.Ala59Pro, XP_047275970.1:p.Ala59Ser, XP_047275971.1:p.Ala59Thr, XP_047275971.1:p.Ala59Pro, XP_047275971.1:p.Ala59Ser, XP_047275968.1:p.Ala59Thr, XP_047275968.1:p.Ala59Pro, XP_047275968.1:p.Ala59Ser, XP_047275976.1:p.Ala59Thr, XP_047275976.1:p.Ala59Pro, XP_047275976.1:p.Ala59Ser

                          13.

                          rs1476203946 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A,C [Show Flanks]
                            Chromosome:
                            7:99619826 (GRCh38)
                            7:99217449 (GRCh37)
                            Canonical SPDI:
                            NC_000007.14:99619825:G:A,NC_000007.14:99619825:G:C
                            Gene:
                            ZSCAN25 (Varview)
                            Functional Consequence:
                            non_coding_transcript_variant,missense_variant,5_prime_UTR_variant,coding_sequence_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            C=0./0 (ALFA)
                            A=0.000011/3 (TOPMED)
                            HGVS:
                            NC_000007.14:g.99619826G>A, NC_000007.14:g.99619826G>C, NC_000007.13:g.99217449G>A, NC_000007.13:g.99217449G>C, XM_011515909.3:c.220G>A, XM_011515909.3:c.220G>C, XM_011515909.2:c.220G>A, XM_011515909.2:c.220G>C, XM_011515909.1:c.220G>A, XM_011515909.1:c.220G>C, NM_145115.3:c.220G>A, NM_145115.3:c.220G>C, NM_145115.2:c.220G>A, NM_145115.2:c.220G>C, XM_011515905.3:c.220G>A, XM_011515905.3:c.220G>C, XM_011515905.2:c.220G>A, XM_011515905.2:c.220G>C, XM_011515905.1:c.220G>A, XM_011515905.1:c.220G>C, XM_011515907.3:c.220G>A, XM_011515907.3:c.220G>C, XM_011515907.2:c.220G>A, XM_011515907.2:c.220G>C, XM_011515907.1:c.220G>A, XM_011515907.1:c.220G>C, XR_927402.3:n.549G>A, XR_927402.3:n.549G>C, XR_927402.2:n.880G>A, XR_927402.2:n.880G>C, XR_927402.1:n.881G>A, XR_927402.1:n.881G>C, XM_011515910.3:c.220G>A, XM_011515910.3:c.220G>C, XM_011515910.2:c.220G>A, XM_011515910.2:c.220G>C, XM_011515910.1:c.220G>A, XM_011515910.1:c.220G>C, NM_001350984.2:c.220G>A, NM_001350984.2:c.220G>C, NM_001350984.1:c.220G>A, NM_001350984.1:c.220G>C, NM_001350980.2:c.220G>A, NM_001350980.2:c.220G>C, NM_001350980.1:c.220G>A, NM_001350980.1:c.220G>C, NM_001350982.2:c.-277G>A, NM_001350982.2:c.-277G>C, NM_001350982.1:c.-277G>A, NM_001350982.1:c.-277G>C, NM_001350985.2:c.220G>A, NM_001350985.2:c.220G>C, NM_001350985.1:c.220G>A, NM_001350985.1:c.220G>C, NM_001350983.2:c.-277G>A, NM_001350983.2:c.-277G>C, NM_001350983.1:c.-277G>A, NM_001350983.1:c.-277G>C, NM_001350981.2:c.-277G>A, NM_001350981.2:c.-277G>C, NM_001350981.1:c.-277G>A, NM_001350981.1:c.-277G>C, NM_001350986.2:c.220G>A, NM_001350986.2:c.220G>C, NM_001350986.1:c.220G>A, NM_001350986.1:c.220G>C, NM_001350979.2:c.220G>A, NM_001350979.2:c.220G>C, NM_001350979.1:c.220G>A, NM_001350979.1:c.220G>C, XM_047420018.1:c.220G>A, XM_047420018.1:c.220G>C, XM_047420016.1:c.220G>A, XM_047420016.1:c.220G>C, XM_047420011.1:c.220G>A, XM_047420011.1:c.220G>C, XM_047420019.1:c.220G>A, XM_047420019.1:c.220G>C, XM_047420017.1:c.220G>A, XM_047420017.1:c.220G>C, XM_047420013.1:c.220G>A, XM_047420013.1:c.220G>C, XM_047420014.1:c.220G>A, XM_047420014.1:c.220G>C, XM_047420015.1:c.220G>A, XM_047420015.1:c.220G>C, XM_047420012.1:c.220G>A, XM_047420012.1:c.220G>C, XR_007059988.1:n.522G>A, XR_007059988.1:n.522G>C, XR_007059989.1:n.464G>A, XR_007059989.1:n.464G>C, XR_007059990.1:n.337G>A, XR_007059990.1:n.337G>C, XM_047420020.1:c.220G>A, XM_047420020.1:c.220G>C, XP_011514211.1:p.Glu74Lys, XP_011514211.1:p.Glu74Gln, NP_660090.2:p.Glu74Lys, NP_660090.2:p.Glu74Gln, XP_011514207.1:p.Glu74Lys, XP_011514207.1:p.Glu74Gln, XP_011514209.1:p.Glu74Lys, XP_011514209.1:p.Glu74Gln, XP_011514212.1:p.Glu74Lys, XP_011514212.1:p.Glu74Gln, NP_001337913.1:p.Glu74Lys, NP_001337913.1:p.Glu74Gln, NP_001337909.1:p.Glu74Lys, NP_001337909.1:p.Glu74Gln, NP_001337914.1:p.Glu74Lys, NP_001337914.1:p.Glu74Gln, NP_001337915.1:p.Glu74Lys, NP_001337915.1:p.Glu74Gln, NP_001337908.1:p.Glu74Lys, NP_001337908.1:p.Glu74Gln, XP_047275974.1:p.Glu74Lys, XP_047275974.1:p.Glu74Gln, XP_047275972.1:p.Glu74Lys, XP_047275972.1:p.Glu74Gln, XP_047275967.1:p.Glu74Lys, XP_047275967.1:p.Glu74Gln, XP_047275975.1:p.Glu74Lys, XP_047275975.1:p.Glu74Gln, XP_047275973.1:p.Glu74Lys, XP_047275973.1:p.Glu74Gln, XP_047275969.1:p.Glu74Lys, XP_047275969.1:p.Glu74Gln, XP_047275970.1:p.Glu74Lys, XP_047275970.1:p.Glu74Gln, XP_047275971.1:p.Glu74Lys, XP_047275971.1:p.Glu74Gln, XP_047275968.1:p.Glu74Lys, XP_047275968.1:p.Glu74Gln, XP_047275976.1:p.Glu74Lys, XP_047275976.1:p.Glu74Gln

                            14.

                            rs1474390019 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>G [Show Flanks]
                              Chromosome:
                              7:99619887 (GRCh38)
                              7:99217510 (GRCh37)
                              Canonical SPDI:
                              NC_000007.14:99619886:T:G
                              Gene:
                              ZSCAN25 (Varview)
                              Functional Consequence:
                              missense_variant,coding_sequence_variant,non_coding_transcript_variant,5_prime_UTR_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              G=0./0 (ALFA)
                              G=0.000004/1 (TOPMED)
                              HGVS:
                              NC_000007.14:g.99619887T>G, NC_000007.13:g.99217510T>G, XM_011515909.3:c.281T>G, XM_011515909.2:c.281T>G, XM_011515909.1:c.281T>G, NM_145115.3:c.281T>G, NM_145115.2:c.281T>G, XM_011515905.3:c.281T>G, XM_011515905.2:c.281T>G, XM_011515905.1:c.281T>G, XM_011515907.3:c.281T>G, XM_011515907.2:c.281T>G, XM_011515907.1:c.281T>G, XR_927402.3:n.610T>G, XR_927402.2:n.941T>G, XR_927402.1:n.942T>G, XM_011515910.3:c.281T>G, XM_011515910.2:c.281T>G, XM_011515910.1:c.281T>G, NM_001350984.2:c.281T>G, NM_001350984.1:c.281T>G, NM_001350980.2:c.281T>G, NM_001350980.1:c.281T>G, NM_001350982.2:c.-216T>G, NM_001350982.1:c.-216T>G, NM_001350985.2:c.281T>G, NM_001350985.1:c.281T>G, NM_001350983.2:c.-216T>G, NM_001350983.1:c.-216T>G, NM_001350981.2:c.-216T>G, NM_001350981.1:c.-216T>G, NM_001350986.2:c.281T>G, NM_001350986.1:c.281T>G, NM_001350979.2:c.281T>G, NM_001350979.1:c.281T>G, XM_047420018.1:c.281T>G, XM_047420016.1:c.281T>G, XM_047420011.1:c.281T>G, XM_047420019.1:c.281T>G, XM_047420017.1:c.281T>G, XM_047420013.1:c.281T>G, XM_047420014.1:c.281T>G, XM_047420015.1:c.281T>G, XM_047420012.1:c.281T>G, XR_007059988.1:n.583T>G, XR_007059989.1:n.525T>G, XR_007059990.1:n.398T>G, XM_047420020.1:c.281T>G, XP_011514211.1:p.Leu94Arg, NP_660090.2:p.Leu94Arg, XP_011514207.1:p.Leu94Arg, XP_011514209.1:p.Leu94Arg, XP_011514212.1:p.Leu94Arg, NP_001337913.1:p.Leu94Arg, NP_001337909.1:p.Leu94Arg, NP_001337914.1:p.Leu94Arg, NP_001337915.1:p.Leu94Arg, NP_001337908.1:p.Leu94Arg, XP_047275974.1:p.Leu94Arg, XP_047275972.1:p.Leu94Arg, XP_047275967.1:p.Leu94Arg, XP_047275975.1:p.Leu94Arg, XP_047275973.1:p.Leu94Arg, XP_047275969.1:p.Leu94Arg, XP_047275970.1:p.Leu94Arg, XP_047275971.1:p.Leu94Arg, XP_047275968.1:p.Leu94Arg, XP_047275976.1:p.Leu94Arg

                              15.

                              rs1471652371 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>T [Show Flanks]
                                Chromosome:
                                7:99621513 (GRCh38)
                                7:99219136 (GRCh37)
                                Canonical SPDI:
                                NC_000007.14:99621512:A:T
                                Gene:
                                ZSCAN25 (Varview)
                                Functional Consequence:
                                synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
                                Validated:
                                by frequency
                                MAF:
                                T=0.000004/1 (GnomAD_exomes)
                                HGVS:
                                NC_000007.14:g.99621513A>T, NC_000007.13:g.99219136A>T, XM_011515909.3:c.528A>T, XM_011515909.2:c.528A>T, XM_011515909.1:c.528A>T, NM_145115.3:c.528A>T, NM_145115.2:c.528A>T, XM_011515905.3:c.528A>T, XM_011515905.2:c.528A>T, XM_011515905.1:c.528A>T, XM_011515907.3:c.528A>T, XM_011515907.2:c.528A>T, XM_011515907.1:c.528A>T, XR_927402.3:n.857A>T, XR_927402.2:n.1188A>T, XR_927402.1:n.1189A>T, XM_011515910.3:c.528A>T, XM_011515910.2:c.528A>T, XM_011515910.1:c.528A>T, NM_001350984.2:c.528A>T, NM_001350984.1:c.528A>T, NM_001350980.2:c.528A>T, NM_001350980.1:c.528A>T, NM_001350982.2:c.36A>T, NM_001350982.1:c.36A>T, NM_001350985.2:c.528A>T, NM_001350985.1:c.528A>T, NM_001350983.2:c.36A>T, NM_001350983.1:c.36A>T, NM_001350981.2:c.36A>T, NM_001350981.1:c.36A>T, NM_001350986.2:c.528A>T, NM_001350986.1:c.528A>T, NM_001350979.2:c.528A>T, NM_001350979.1:c.528A>T, XM_047420018.1:c.528A>T, XM_047420016.1:c.528A>T, XM_047420011.1:c.528A>T, XM_047420019.1:c.528A>T, XM_047420017.1:c.528A>T, XM_047420013.1:c.528A>T, XM_047420014.1:c.528A>T, XM_047420015.1:c.528A>T, XM_047420012.1:c.528A>T, XR_007059988.1:n.830A>T, XR_007059989.1:n.772A>T, XR_007059990.1:n.645A>T, XM_047420020.1:c.528A>T

                                16.

                                rs1471282470 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  A>G [Show Flanks]
                                  Chromosome:
                                  7:99629615 (GRCh38)
                                  7:99227238 (GRCh37)
                                  Canonical SPDI:
                                  NC_000007.14:99629614:A:G
                                  Gene:
                                  ZSCAN25 (Varview)
                                  Functional Consequence:
                                  3_prime_UTR_variant,coding_sequence_variant,synonymous_variant,intron_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  G=0./0 (ALFA)
                                  G=0.000008/2 (TOPMED)
                                  HGVS:

                                  17.

                                  rs1469848910 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>A [Show Flanks]
                                    Chromosome:
                                    7:99619889 (GRCh38)
                                    7:99217512 (GRCh37)
                                    Canonical SPDI:
                                    NC_000007.14:99619888:C:A
                                    Gene:
                                    ZSCAN25 (Varview)
                                    Functional Consequence:
                                    missense_variant,coding_sequence_variant,non_coding_transcript_variant,5_prime_UTR_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    A=0.000071/1 (ALFA)
                                    A=0.000019/5 (TOPMED)
                                    A=0.000036/5 (GnomAD)
                                    HGVS:
                                    NC_000007.14:g.99619889C>A, NC_000007.13:g.99217512C>A, XM_011515909.3:c.283C>A, XM_011515909.2:c.283C>A, XM_011515909.1:c.283C>A, NM_145115.3:c.283C>A, NM_145115.2:c.283C>A, XM_011515905.3:c.283C>A, XM_011515905.2:c.283C>A, XM_011515905.1:c.283C>A, XM_011515907.3:c.283C>A, XM_011515907.2:c.283C>A, XM_011515907.1:c.283C>A, XR_927402.3:n.612C>A, XR_927402.2:n.943C>A, XR_927402.1:n.944C>A, XM_011515910.3:c.283C>A, XM_011515910.2:c.283C>A, XM_011515910.1:c.283C>A, NM_001350984.2:c.283C>A, NM_001350984.1:c.283C>A, NM_001350980.2:c.283C>A, NM_001350980.1:c.283C>A, NM_001350982.2:c.-214C>A, NM_001350982.1:c.-214C>A, NM_001350985.2:c.283C>A, NM_001350985.1:c.283C>A, NM_001350983.2:c.-214C>A, NM_001350983.1:c.-214C>A, NM_001350981.2:c.-214C>A, NM_001350981.1:c.-214C>A, NM_001350986.2:c.283C>A, NM_001350986.1:c.283C>A, NM_001350979.2:c.283C>A, NM_001350979.1:c.283C>A, XM_047420018.1:c.283C>A, XM_047420016.1:c.283C>A, XM_047420011.1:c.283C>A, XM_047420019.1:c.283C>A, XM_047420017.1:c.283C>A, XM_047420013.1:c.283C>A, XM_047420014.1:c.283C>A, XM_047420015.1:c.283C>A, XM_047420012.1:c.283C>A, XR_007059988.1:n.585C>A, XR_007059989.1:n.527C>A, XR_007059990.1:n.400C>A, XM_047420020.1:c.283C>A, XP_011514211.1:p.Pro95Thr, NP_660090.2:p.Pro95Thr, XP_011514207.1:p.Pro95Thr, XP_011514209.1:p.Pro95Thr, XP_011514212.1:p.Pro95Thr, NP_001337913.1:p.Pro95Thr, NP_001337909.1:p.Pro95Thr, NP_001337914.1:p.Pro95Thr, NP_001337915.1:p.Pro95Thr, NP_001337908.1:p.Pro95Thr, XP_047275974.1:p.Pro95Thr, XP_047275972.1:p.Pro95Thr, XP_047275967.1:p.Pro95Thr, XP_047275975.1:p.Pro95Thr, XP_047275973.1:p.Pro95Thr, XP_047275969.1:p.Pro95Thr, XP_047275970.1:p.Pro95Thr, XP_047275971.1:p.Pro95Thr, XP_047275968.1:p.Pro95Thr, XP_047275976.1:p.Pro95Thr

                                    18.

                                    rs1468512349 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C [Show Flanks]
                                      Chromosome:
                                      7:99629386 (GRCh38)
                                      7:99227009 (GRCh37)
                                      Canonical SPDI:
                                      NC_000007.14:99629385:T:C
                                      Gene:
                                      ZSCAN25 (Varview)
                                      Functional Consequence:
                                      3_prime_UTR_variant,coding_sequence_variant,missense_variant,intron_variant
                                      Validated:
                                      by frequency
                                      MAF:
                                      C=0.000004/1 (GnomAD_exomes)
                                      HGVS:
                                      NC_000007.14:g.99629386T>C, NC_000007.13:g.99227009T>C, NM_145115.3:c.1001T>C, NM_145115.2:c.1001T>C, XM_011515905.3:c.1001T>C, XM_011515905.2:c.1001T>C, XM_011515905.1:c.1001T>C, XM_011515907.3:c.1001T>C, XM_011515907.2:c.1001T>C, XM_011515907.1:c.1001T>C, NM_001350980.2:c.1001T>C, NM_001350980.1:c.1001T>C, NM_001350982.2:c.509T>C, NM_001350982.1:c.509T>C, NM_001350983.2:c.509T>C, NM_001350983.1:c.509T>C, NM_001350981.2:c.509T>C, NM_001350981.1:c.509T>C, NM_001350986.2:c.*148T>C, NM_001350986.1:c.*148T>C, NM_001350979.2:c.1001T>C, NM_001350979.1:c.1001T>C, XM_047420011.1:c.1001T>C, XM_047420013.1:c.1001T>C, XM_047420014.1:c.1001T>C, XM_047420015.1:c.1001T>C, XM_047420012.1:c.1001T>C, NP_660090.2:p.Leu334Pro, XP_011514207.1:p.Leu334Pro, XP_011514209.1:p.Leu334Pro, NP_001337909.1:p.Leu334Pro, NP_001337911.1:p.Leu170Pro, NP_001337912.1:p.Leu170Pro, NP_001337910.1:p.Leu170Pro, NP_001337908.1:p.Leu334Pro, XP_047275967.1:p.Leu334Pro, XP_047275969.1:p.Leu334Pro, XP_047275970.1:p.Leu334Pro, XP_047275971.1:p.Leu334Pro, XP_047275968.1:p.Leu334Pro

                                      19.

                                      rs1464320510 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G [Show Flanks]
                                        Chromosome:
                                        7:99629955 (GRCh38)
                                        7:99227578 (GRCh37)
                                        Canonical SPDI:
                                        NC_000007.14:99629954:A:G
                                        Gene:
                                        ZSCAN25 (Varview)
                                        Functional Consequence:
                                        3_prime_UTR_variant,coding_sequence_variant,missense_variant,intron_variant
                                        Validated:
                                        by frequency
                                        MAF:
                                        G=0.000004/1 (GnomAD_exomes)
                                        HGVS:
                                        NC_000007.14:g.99629955A>G, NC_000007.13:g.99227578A>G, NM_145115.3:c.1570A>G, NM_145115.2:c.1570A>G, XM_011515905.3:c.1570A>G, XM_011515905.2:c.1570A>G, XM_011515905.1:c.1570A>G, XM_011515907.3:c.1570A>G, XM_011515907.2:c.1570A>G, XM_011515907.1:c.1570A>G, NM_001350980.2:c.1570A>G, NM_001350980.1:c.1570A>G, NM_001350982.2:c.1078A>G, NM_001350982.1:c.1078A>G, NM_001350983.2:c.1078A>G, NM_001350983.1:c.1078A>G, NM_001350981.2:c.1078A>G, NM_001350981.1:c.1078A>G, NM_001350986.2:c.*717A>G, NM_001350986.1:c.*717A>G, NM_001350979.2:c.1570A>G, NM_001350979.1:c.1570A>G, XM_047420011.1:c.1570A>G, XM_047420013.1:c.1570A>G, XM_047420014.1:c.1570A>G, XM_047420015.1:c.1570A>G, XM_047420012.1:c.1570A>G, NP_660090.2:p.Asn524Asp, XP_011514207.1:p.Asn524Asp, XP_011514209.1:p.Asn524Asp, NP_001337909.1:p.Asn524Asp, NP_001337911.1:p.Asn360Asp, NP_001337912.1:p.Asn360Asp, NP_001337910.1:p.Asn360Asp, NP_001337908.1:p.Asn524Asp, XP_047275967.1:p.Asn524Asp, XP_047275969.1:p.Asn524Asp, XP_047275970.1:p.Asn524Asp, XP_047275971.1:p.Asn524Asp, XP_047275968.1:p.Asn524Asp

                                        20.

                                        rs1461183558 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          7:99624063 (GRCh38)
                                          7:99221686 (GRCh37)
                                          Canonical SPDI:
                                          NC_000007.14:99624062:G:A
                                          Gene:
                                          ZSCAN25 (Varview)
                                          Functional Consequence:
                                          non_coding_transcript_variant,coding_sequence_variant,intron_variant,missense_variant
                                          Validated:
                                          by frequency
                                          MAF:
                                          A=0.000004/1 (GnomAD_exomes)
                                          HGVS:
                                          NC_000007.14:g.99624063G>A, NC_000007.13:g.99221686G>A, XM_011515909.3:c.688G>A, XM_011515909.2:c.688G>A, XM_011515909.1:c.688G>A, NM_145115.3:c.688G>A, NM_145115.2:c.688G>A, XM_011515905.3:c.688G>A, XM_011515905.2:c.688G>A, XM_011515905.1:c.688G>A, XM_011515907.3:c.688G>A, XM_011515907.2:c.688G>A, XM_011515907.1:c.688G>A, XR_927402.3:n.1017G>A, XR_927402.2:n.1348G>A, XR_927402.1:n.1349G>A, XM_011515910.3:c.688G>A, XM_011515910.2:c.688G>A, XM_011515910.1:c.688G>A, NM_001350984.2:c.688G>A, NM_001350984.1:c.688G>A, NM_001350980.2:c.688G>A, NM_001350980.1:c.688G>A, NM_001350982.2:c.196G>A, NM_001350982.1:c.196G>A, NM_001350985.2:c.688G>A, NM_001350985.1:c.688G>A, NM_001350983.2:c.196G>A, NM_001350983.1:c.196G>A, NM_001350981.2:c.196G>A, NM_001350981.1:c.196G>A, NM_001350979.2:c.688G>A, NM_001350979.1:c.688G>A, XM_047420018.1:c.688G>A, XM_047420016.1:c.688G>A, XM_047420011.1:c.688G>A, XM_047420019.1:c.688G>A, XM_047420017.1:c.688G>A, XM_047420013.1:c.688G>A, XM_047420014.1:c.688G>A, XM_047420015.1:c.688G>A, XM_047420012.1:c.688G>A, XR_007059988.1:n.990G>A, XR_007059989.1:n.932G>A, XR_007059990.1:n.805G>A, XM_047420020.1:c.688G>A, XP_011514211.1:p.Gly230Arg, NP_660090.2:p.Gly230Arg, XP_011514207.1:p.Gly230Arg, XP_011514209.1:p.Gly230Arg, XP_011514212.1:p.Gly230Arg, NP_001337913.1:p.Gly230Arg, NP_001337909.1:p.Gly230Arg, NP_001337911.1:p.Gly66Arg, NP_001337914.1:p.Gly230Arg, NP_001337912.1:p.Gly66Arg, NP_001337910.1:p.Gly66Arg, NP_001337908.1:p.Gly230Arg, XP_047275974.1:p.Gly230Arg, XP_047275972.1:p.Gly230Arg, XP_047275967.1:p.Gly230Arg, XP_047275975.1:p.Gly230Arg, XP_047275973.1:p.Gly230Arg, XP_047275969.1:p.Gly230Arg, XP_047275970.1:p.Gly230Arg, XP_047275971.1:p.Gly230Arg, XP_047275968.1:p.Gly230Arg, XP_047275976.1:p.Gly230Arg

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