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Items: 1 to 20 of 539

1.

rs1489490153 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    1:157768421 (GRCh38)
    1:157738211 (GRCh37)
    Canonical SPDI:
    NC_000001.11:157768420:A:G
    Gene:
    FCRL2 (Varview)
    Functional Consequence:
    non_coding_transcript_variant,intron_variant,synonymous_variant,coding_sequence_variant
    Validated:
    by frequency,by alfa
    MAF:
    G=0./0 (ALFA)
    G=0.000004/1 (TOPMED)
    HGVS:
    NC_000001.11:g.157768421A>G, NC_000001.10:g.157738211A>G, XM_011509974.4:c.876T>C, XM_011509974.3:c.876T>C, XM_011509974.2:c.876T>C, XM_011509974.1:c.876T>C, NM_030764.4:c.876T>C, NM_030764.3:c.876T>C, XM_011509975.4:c.876T>C, XM_011509975.3:c.876T>C, XM_011509975.2:c.876T>C, XM_011509975.1:c.876T>C, XM_006711535.4:c.876T>C, XM_006711535.3:c.876T>C, XM_006711535.2:c.876T>C, XM_006711535.1:c.876T>C, XM_011509976.3:c.876T>C, XM_011509976.2:c.876T>C, XM_011509976.1:c.876T>C, XM_017002316.2:c.876T>C, XM_017002316.1:c.876T>C, NM_001159488.2:c.876T>C, NM_001159488.1:c.876T>C, XM_017002317.2:c.876T>C, XM_017002317.1:c.876T>C, XM_017002318.2:c.876T>C, XM_017002318.1:c.876T>C, XM_017002319.2:c.591T>C, XM_017002319.1:c.591T>C, XR_001737403.2:n.935T>C, XR_001737403.1:n.1274T>C, XR_001737404.2:n.935T>C, XR_001737404.1:n.1274T>C, XM_047430270.1:c.876T>C, XM_047430273.1:c.591T>C, XM_047430275.1:c.591T>C

    2.

    rs1489110178 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>G [Show Flanks]
      Chromosome:
      1:157767258 (GRCh38)
      1:157737048 (GRCh37)
      Canonical SPDI:
      NC_000001.11:157767257:T:G
      Gene:
      FCRL2 (Varview)
      Functional Consequence:
      intron_variant,genic_downstream_transcript_variant,coding_sequence_variant,downstream_transcript_variant,missense_variant
      HGVS:
      NC_000001.11:g.157767258T>G, NC_000001.10:g.157737048T>G, XM_011509974.4:c.1135A>C, XM_011509974.3:c.1135A>C, XM_011509974.2:c.1135A>C, XM_011509974.1:c.1135A>C, NM_030764.4:c.1135A>C, NM_030764.3:c.1135A>C, XM_011509975.4:c.1135A>C, XM_011509975.3:c.1135A>C, XM_011509975.2:c.1135A>C, XM_011509975.1:c.1135A>C, XM_011509976.3:c.1135A>C, XM_011509976.2:c.1135A>C, XM_011509976.1:c.1135A>C, XM_017002316.2:c.1135A>C, XM_017002316.1:c.1135A>C, NM_001159488.2:c.1135A>C, NM_001159488.1:c.1135A>C, XM_017002317.2:c.937A>C, XM_017002317.1:c.937A>C, XM_017002319.2:c.850A>C, XM_017002319.1:c.850A>C, XM_047430273.1:c.850A>C, NM_138739.1:c.376A>C, XP_011508276.1:p.Ser379Arg, NP_110391.2:p.Ser379Arg, XP_011508277.1:p.Ser379Arg, XP_011508278.1:p.Ser379Arg, XP_016857805.1:p.Ser379Arg, NP_001152960.1:p.Ser379Arg, XP_016857806.1:p.Ser313Arg, XP_016857808.1:p.Ser284Arg, XP_047286229.1:p.Ser284Arg

      3.

      rs1489047014 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>T [Show Flanks]
        Chromosome:
        1:157767426 (GRCh38)
        1:157737216 (GRCh37)
        Canonical SPDI:
        NC_000001.11:157767425:C:T
        Gene:
        FCRL2 (Varview)
        Functional Consequence:
        intron_variant,genic_downstream_transcript_variant,coding_sequence_variant,synonymous_variant,downstream_transcript_variant,non_coding_transcript_variant,missense_variant
        Validated:
        by frequency
        MAF:
        T=0.000012/3 (GnomAD_exomes)
        HGVS:
        NC_000001.11:g.157767426C>T, NC_000001.10:g.157737216C>T, XM_011509974.4:c.967G>A, XM_011509974.3:c.967G>A, XM_011509974.2:c.967G>A, XM_011509974.1:c.967G>A, NM_030764.4:c.967G>A, NM_030764.3:c.967G>A, XM_011509975.4:c.967G>A, XM_011509975.3:c.967G>A, XM_011509975.2:c.967G>A, XM_011509975.1:c.967G>A, XM_006711535.4:c.936G>A, XM_006711535.3:c.936G>A, XM_006711535.2:c.936G>A, XM_006711535.1:c.936G>A, XM_011509976.3:c.967G>A, XM_011509976.2:c.967G>A, XM_011509976.1:c.967G>A, XM_017002316.2:c.967G>A, XM_017002316.1:c.967G>A, NM_001159488.2:c.967G>A, NM_001159488.1:c.967G>A, XM_017002319.2:c.682G>A, XM_017002319.1:c.682G>A, XR_001737404.2:n.1138G>A, XR_001737404.1:n.1477G>A, XM_047430273.1:c.682G>A, NM_138739.1:c.208G>A, XP_011508276.1:p.Ala323Thr, NP_110391.2:p.Ala323Thr, XP_011508277.1:p.Ala323Thr, XP_011508278.1:p.Ala323Thr, XP_016857805.1:p.Ala323Thr, NP_001152960.1:p.Ala323Thr, XP_016857808.1:p.Ala228Thr, XP_047286229.1:p.Ala228Thr

        4.

        rs1488977637 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          T>C [Show Flanks]
          Chromosome:
          1:157768643 (GRCh38)
          1:157738433 (GRCh37)
          Canonical SPDI:
          NC_000001.11:157768642:T:C
          Gene:
          FCRL2 (Varview)
          Functional Consequence:
          non_coding_transcript_variant,intron_variant,synonymous_variant,coding_sequence_variant
          Validated:
          by frequency,by alfa
          MAF:
          C=0.000111/1 (ALFA)
          C=0.000004/1 (GnomAD_exomes)
          HGVS:
          NC_000001.11:g.157768643T>C, NC_000001.10:g.157738433T>C, XM_011509974.4:c.654A>G, XM_011509974.3:c.654A>G, XM_011509974.2:c.654A>G, XM_011509974.1:c.654A>G, NM_030764.4:c.654A>G, NM_030764.3:c.654A>G, XM_011509975.4:c.654A>G, XM_011509975.3:c.654A>G, XM_011509975.2:c.654A>G, XM_011509975.1:c.654A>G, XM_006711535.4:c.654A>G, XM_006711535.3:c.654A>G, XM_006711535.2:c.654A>G, XM_006711535.1:c.654A>G, XM_011509976.3:c.654A>G, XM_011509976.2:c.654A>G, XM_011509976.1:c.654A>G, XM_017002316.2:c.654A>G, XM_017002316.1:c.654A>G, NM_001159488.2:c.654A>G, NM_001159488.1:c.654A>G, XM_017002317.2:c.654A>G, XM_017002317.1:c.654A>G, XM_017002318.2:c.654A>G, XM_017002318.1:c.654A>G, XM_017002319.2:c.369A>G, XM_017002319.1:c.369A>G, XR_001737403.2:n.713A>G, XR_001737403.1:n.1052A>G, XR_001737404.2:n.713A>G, XR_001737404.1:n.1052A>G, XM_047430270.1:c.654A>G, XM_047430273.1:c.369A>G, XM_047430275.1:c.369A>G

          5.

          rs1488678373 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>C [Show Flanks]
            Chromosome:
            1:157770596 (GRCh38)
            1:157740386 (GRCh37)
            Canonical SPDI:
            NC_000001.11:157770595:T:C
            Gene:
            FCRL2 (Varview)
            Functional Consequence:
            non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
            Validated:
            by frequency,by alfa
            MAF:
            C=0./0 (ALFA)
            C=0.000004/1 (TOPMED)
            HGVS:
            NC_000001.11:g.157770596T>C, NC_000001.10:g.157740386T>C, NG_082207.1:g.1082T>C, XM_011509974.4:c.123A>G, XM_011509974.3:c.123A>G, XM_011509974.2:c.123A>G, XM_011509974.1:c.123A>G, NM_030764.4:c.123A>G, NM_030764.3:c.123A>G, XM_011509975.4:c.123A>G, XM_011509975.3:c.123A>G, XM_011509975.2:c.123A>G, XM_011509975.1:c.123A>G, XM_006711535.4:c.123A>G, XM_006711535.3:c.123A>G, XM_006711535.2:c.123A>G, XM_006711535.1:c.123A>G, XM_011509976.3:c.123A>G, XM_011509976.2:c.123A>G, XM_011509976.1:c.123A>G, XM_017002316.2:c.123A>G, XM_017002316.1:c.123A>G, NM_001159488.2:c.123A>G, NM_001159488.1:c.123A>G, XM_017002317.2:c.123A>G, XM_017002317.1:c.123A>G, XM_017002318.2:c.123A>G, XM_017002318.1:c.123A>G, XM_017002319.2:c.123A>G, XM_017002319.1:c.123A>G, NR_125358.2:n.182A>G, NR_125358.1:n.182A>G, XR_001737403.2:n.182A>G, XR_001737403.1:n.521A>G, XR_001737404.2:n.182A>G, XR_001737404.1:n.521A>G, XM_047430270.1:c.123A>G, XM_047430273.1:c.123A>G, XM_047430275.1:c.123A>G

            6.

            rs1486797536 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>A,C [Show Flanks]
              Chromosome:
              1:157770658 (GRCh38)
              1:157740448 (GRCh37)
              Canonical SPDI:
              NC_000001.11:157770657:T:A,NC_000001.11:157770657:T:C
              Gene:
              FCRL2 (Varview)
              Functional Consequence:
              non_coding_transcript_variant,missense_variant,coding_sequence_variant
              Validated:
              by frequency,by alfa
              MAF:
              A=0./0 (ALFA)
              C=0.000004/1 (GnomAD_exomes)
              HGVS:
              NC_000001.11:g.157770658T>A, NC_000001.11:g.157770658T>C, NC_000001.10:g.157740448T>A, NC_000001.10:g.157740448T>C, NG_082207.1:g.1144T>A, NG_082207.1:g.1144T>C, XM_011509974.4:c.61A>T, XM_011509974.4:c.61A>G, XM_011509974.3:c.61A>T, XM_011509974.3:c.61A>G, XM_011509974.2:c.61A>T, XM_011509974.2:c.61A>G, XM_011509974.1:c.61A>T, XM_011509974.1:c.61A>G, NM_030764.4:c.61A>T, NM_030764.4:c.61A>G, NM_030764.3:c.61A>T, NM_030764.3:c.61A>G, XM_011509975.4:c.61A>T, XM_011509975.4:c.61A>G, XM_011509975.3:c.61A>T, XM_011509975.3:c.61A>G, XM_011509975.2:c.61A>T, XM_011509975.2:c.61A>G, XM_011509975.1:c.61A>T, XM_011509975.1:c.61A>G, XM_006711535.4:c.61A>T, XM_006711535.4:c.61A>G, XM_006711535.3:c.61A>T, XM_006711535.3:c.61A>G, XM_006711535.2:c.61A>T, XM_006711535.2:c.61A>G, XM_006711535.1:c.61A>T, XM_006711535.1:c.61A>G, XM_011509976.3:c.61A>T, XM_011509976.3:c.61A>G, XM_011509976.2:c.61A>T, XM_011509976.2:c.61A>G, XM_011509976.1:c.61A>T, XM_011509976.1:c.61A>G, XM_017002316.2:c.61A>T, XM_017002316.2:c.61A>G, XM_017002316.1:c.61A>T, XM_017002316.1:c.61A>G, NM_001159488.2:c.61A>T, NM_001159488.2:c.61A>G, NM_001159488.1:c.61A>T, NM_001159488.1:c.61A>G, XM_017002317.2:c.61A>T, XM_017002317.2:c.61A>G, XM_017002317.1:c.61A>T, XM_017002317.1:c.61A>G, XM_017002318.2:c.61A>T, XM_017002318.2:c.61A>G, XM_017002318.1:c.61A>T, XM_017002318.1:c.61A>G, XM_017002319.2:c.61A>T, XM_017002319.2:c.61A>G, XM_017002319.1:c.61A>T, XM_017002319.1:c.61A>G, NR_125358.2:n.120A>T, NR_125358.2:n.120A>G, NR_125358.1:n.120A>T, NR_125358.1:n.120A>G, XR_001737403.2:n.120A>T, XR_001737403.2:n.120A>G, XR_001737403.1:n.459A>T, XR_001737403.1:n.459A>G, XR_001737404.2:n.120A>T, XR_001737404.2:n.120A>G, XR_001737404.1:n.459A>T, XR_001737404.1:n.459A>G, XM_047430270.1:c.61A>T, XM_047430270.1:c.61A>G, XM_047430273.1:c.61A>T, XM_047430273.1:c.61A>G, XM_047430275.1:c.61A>T, XM_047430275.1:c.61A>G, XP_011508276.1:p.Thr21Ser, XP_011508276.1:p.Thr21Ala, NP_110391.2:p.Thr21Ser, NP_110391.2:p.Thr21Ala, XP_011508277.1:p.Thr21Ser, XP_011508277.1:p.Thr21Ala, XP_006711598.1:p.Thr21Ser, XP_006711598.1:p.Thr21Ala, XP_011508278.1:p.Thr21Ser, XP_011508278.1:p.Thr21Ala, XP_016857805.1:p.Thr21Ser, XP_016857805.1:p.Thr21Ala, NP_001152960.1:p.Thr21Ser, NP_001152960.1:p.Thr21Ala, XP_016857806.1:p.Thr21Ser, XP_016857806.1:p.Thr21Ala, XP_016857807.1:p.Thr21Ser, XP_016857807.1:p.Thr21Ala, XP_016857808.1:p.Thr21Ser, XP_016857808.1:p.Thr21Ala, XP_047286226.1:p.Thr21Ser, XP_047286226.1:p.Thr21Ala, XP_047286229.1:p.Thr21Ser, XP_047286229.1:p.Thr21Ala, XP_047286231.1:p.Thr21Ser, XP_047286231.1:p.Thr21Ala

              7.

              rs1481556912 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                A>C [Show Flanks]
                Chromosome:
                1:157770044 (GRCh38)
                1:157739834 (GRCh37)
                Canonical SPDI:
                NC_000001.11:157770043:A:C
                Gene:
                FCRL2 (Varview)
                Functional Consequence:
                non_coding_transcript_variant,intron_variant,coding_sequence_variant,synonymous_variant
                Validated:
                by frequency
                MAF:
                C=0.000004/1 (GnomAD_exomes)
                HGVS:
                NC_000001.11:g.157770044A>C, NC_000001.10:g.157739834A>C, NG_082207.1:g.530A>C, XM_011509974.4:c.417T>G, XM_011509974.3:c.417T>G, XM_011509974.2:c.417T>G, XM_011509974.1:c.417T>G, NM_030764.4:c.417T>G, NM_030764.3:c.417T>G, XM_011509975.4:c.417T>G, XM_011509975.3:c.417T>G, XM_011509975.2:c.417T>G, XM_011509975.1:c.417T>G, XM_006711535.4:c.417T>G, XM_006711535.3:c.417T>G, XM_006711535.2:c.417T>G, XM_006711535.1:c.417T>G, XM_011509976.3:c.417T>G, XM_011509976.2:c.417T>G, XM_011509976.1:c.417T>G, XM_017002316.2:c.417T>G, XM_017002316.1:c.417T>G, NM_001159488.2:c.417T>G, NM_001159488.1:c.417T>G, XM_017002317.2:c.417T>G, XM_017002317.1:c.417T>G, XM_017002318.2:c.417T>G, XM_017002318.1:c.417T>G, XR_001737403.2:n.476T>G, XR_001737403.1:n.815T>G, XR_001737404.2:n.476T>G, XR_001737404.1:n.815T>G, XM_047430270.1:c.417T>G

                8.

                rs1479930133 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  1:157770542 (GRCh38)
                  1:157740332 (GRCh37)
                  Canonical SPDI:
                  NC_000001.11:157770541:A:G
                  Gene:
                  FCRL2 (Varview)
                  Functional Consequence:
                  non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
                  Validated:
                  by frequency
                  MAF:
                  G=0.000004/1 (GnomAD_exomes)
                  HGVS:
                  NC_000001.11:g.157770542A>G, NC_000001.10:g.157740332A>G, NG_082207.1:g.1028A>G, XM_011509974.4:c.177T>C, XM_011509974.3:c.177T>C, XM_011509974.2:c.177T>C, XM_011509974.1:c.177T>C, NM_030764.4:c.177T>C, NM_030764.3:c.177T>C, XM_011509975.4:c.177T>C, XM_011509975.3:c.177T>C, XM_011509975.2:c.177T>C, XM_011509975.1:c.177T>C, XM_006711535.4:c.177T>C, XM_006711535.3:c.177T>C, XM_006711535.2:c.177T>C, XM_006711535.1:c.177T>C, XM_011509976.3:c.177T>C, XM_011509976.2:c.177T>C, XM_011509976.1:c.177T>C, XM_017002316.2:c.177T>C, XM_017002316.1:c.177T>C, NM_001159488.2:c.177T>C, NM_001159488.1:c.177T>C, XM_017002317.2:c.177T>C, XM_017002317.1:c.177T>C, XM_017002318.2:c.177T>C, XM_017002318.1:c.177T>C, XM_017002319.2:c.177T>C, XM_017002319.1:c.177T>C, NR_125358.2:n.236T>C, NR_125358.1:n.236T>C, XR_001737403.2:n.236T>C, XR_001737403.1:n.575T>C, XR_001737404.2:n.236T>C, XR_001737404.1:n.575T>C, XM_047430270.1:c.177T>C, XM_047430273.1:c.177T>C, XM_047430275.1:c.177T>C

                  9.

                  rs1478853253 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>G [Show Flanks]
                    Chromosome:
                    1:157749658 (GRCh38)
                    1:157719448 (GRCh37)
                    Canonical SPDI:
                    NC_000001.11:157749657:A:G
                    Gene:
                    FCRL2 (Varview)
                    Functional Consequence:
                    non_coding_transcript_variant,coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    G=0./0 (ALFA)
                    G=0.000008/2 (GnomAD_exomes)
                    HGVS:

                    10.

                    rs1476797884 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      A>T [Show Flanks]
                      Chromosome:
                      1:157770547 (GRCh38)
                      1:157740337 (GRCh37)
                      Canonical SPDI:
                      NC_000001.11:157770546:A:T
                      Gene:
                      FCRL2 (Varview)
                      Functional Consequence:
                      non_coding_transcript_variant,coding_sequence_variant,missense_variant
                      Validated:
                      by frequency
                      MAF:
                      T=0.000004/1 (GnomAD_exomes)
                      HGVS:
                      NC_000001.11:g.157770547A>T, NC_000001.10:g.157740337A>T, NG_082207.1:g.1033A>T, XM_011509974.4:c.172T>A, XM_011509974.3:c.172T>A, XM_011509974.2:c.172T>A, XM_011509974.1:c.172T>A, NM_030764.4:c.172T>A, NM_030764.3:c.172T>A, XM_011509975.4:c.172T>A, XM_011509975.3:c.172T>A, XM_011509975.2:c.172T>A, XM_011509975.1:c.172T>A, XM_006711535.4:c.172T>A, XM_006711535.3:c.172T>A, XM_006711535.2:c.172T>A, XM_006711535.1:c.172T>A, XM_011509976.3:c.172T>A, XM_011509976.2:c.172T>A, XM_011509976.1:c.172T>A, XM_017002316.2:c.172T>A, XM_017002316.1:c.172T>A, NM_001159488.2:c.172T>A, NM_001159488.1:c.172T>A, XM_017002317.2:c.172T>A, XM_017002317.1:c.172T>A, XM_017002318.2:c.172T>A, XM_017002318.1:c.172T>A, XM_017002319.2:c.172T>A, XM_017002319.1:c.172T>A, NR_125358.2:n.231T>A, NR_125358.1:n.231T>A, XR_001737403.2:n.231T>A, XR_001737403.1:n.570T>A, XR_001737404.2:n.231T>A, XR_001737404.1:n.570T>A, XM_047430270.1:c.172T>A, XM_047430273.1:c.172T>A, XM_047430275.1:c.172T>A, XP_011508276.1:p.Leu58Ile, NP_110391.2:p.Leu58Ile, XP_011508277.1:p.Leu58Ile, XP_006711598.1:p.Leu58Ile, XP_011508278.1:p.Leu58Ile, XP_016857805.1:p.Leu58Ile, NP_001152960.1:p.Leu58Ile, XP_016857806.1:p.Leu58Ile, XP_016857807.1:p.Leu58Ile, XP_016857808.1:p.Leu58Ile, XP_047286226.1:p.Leu58Ile, XP_047286229.1:p.Leu58Ile, XP_047286231.1:p.Leu58Ile

                      11.

                      rs1476649618 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>A [Show Flanks]
                        Chromosome:
                        1:157768649 (GRCh38)
                        1:157738439 (GRCh37)
                        Canonical SPDI:
                        NC_000001.11:157768648:C:A
                        Gene:
                        FCRL2 (Varview)
                        Functional Consequence:
                        non_coding_transcript_variant,intron_variant,coding_sequence_variant,synonymous_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        A=0.000043/1 (ALFA)
                        A=0.000004/1 (TOPMED)
                        A=0.000007/1 (GnomAD)
                        A=0.000016/4 (GnomAD_exomes)
                        HGVS:
                        NC_000001.11:g.157768649C>A, NC_000001.10:g.157738439C>A, XM_011509974.4:c.648G>T, XM_011509974.3:c.648G>T, XM_011509974.2:c.648G>T, XM_011509974.1:c.648G>T, NM_030764.4:c.648G>T, NM_030764.3:c.648G>T, XM_011509975.4:c.648G>T, XM_011509975.3:c.648G>T, XM_011509975.2:c.648G>T, XM_011509975.1:c.648G>T, XM_006711535.4:c.648G>T, XM_006711535.3:c.648G>T, XM_006711535.2:c.648G>T, XM_006711535.1:c.648G>T, XM_011509976.3:c.648G>T, XM_011509976.2:c.648G>T, XM_011509976.1:c.648G>T, XM_017002316.2:c.648G>T, XM_017002316.1:c.648G>T, NM_001159488.2:c.648G>T, NM_001159488.1:c.648G>T, XM_017002317.2:c.648G>T, XM_017002317.1:c.648G>T, XM_017002318.2:c.648G>T, XM_017002318.1:c.648G>T, XM_017002319.2:c.363G>T, XM_017002319.1:c.363G>T, XR_001737403.2:n.707G>T, XR_001737403.1:n.1046G>T, XR_001737404.2:n.707G>T, XR_001737404.1:n.1046G>T, XM_047430270.1:c.648G>T, XM_047430273.1:c.363G>T, XM_047430275.1:c.363G>T

                        12.

                        rs1475661811 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          1:157769978 (GRCh38)
                          1:157739768 (GRCh37)
                          Canonical SPDI:
                          NC_000001.11:157769977:C:T
                          Gene:
                          FCRL2 (Varview)
                          Functional Consequence:
                          synonymous_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          T=0./0 (ALFA)
                          T=0.000004/1 (TOPMED)
                          T=0.000007/1 (GnomAD)
                          HGVS:
                          NC_000001.11:g.157769978C>T, NC_000001.10:g.157739768C>T, NG_082207.1:g.464C>T, XM_011509974.4:c.483G>A, XM_011509974.3:c.483G>A, XM_011509974.2:c.483G>A, XM_011509974.1:c.483G>A, NM_030764.4:c.483G>A, NM_030764.3:c.483G>A, XM_011509975.4:c.483G>A, XM_011509975.3:c.483G>A, XM_011509975.2:c.483G>A, XM_011509975.1:c.483G>A, XM_006711535.4:c.483G>A, XM_006711535.3:c.483G>A, XM_006711535.2:c.483G>A, XM_006711535.1:c.483G>A, XM_011509976.3:c.483G>A, XM_011509976.2:c.483G>A, XM_011509976.1:c.483G>A, XM_017002316.2:c.483G>A, XM_017002316.1:c.483G>A, NM_001159488.2:c.483G>A, NM_001159488.1:c.483G>A, XM_017002317.2:c.483G>A, XM_017002317.1:c.483G>A, XM_017002318.2:c.483G>A, XM_017002318.1:c.483G>A, XR_001737403.2:n.542G>A, XR_001737403.1:n.881G>A, XR_001737404.2:n.542G>A, XR_001737404.1:n.881G>A, XM_047430270.1:c.483G>A

                          13.

                          rs1472805145 [Homo sapiens]
                            Variant type:
                            DEL
                            Alleles:
                            C>- [Show Flanks]
                            Chromosome:
                            1:157767431 (GRCh38)
                            1:157737221 (GRCh37)
                            Canonical SPDI:
                            NC_000001.11:157767430:C:
                            Gene:
                            FCRL2 (Varview)
                            Functional Consequence:
                            stop_gained,coding_sequence_variant,frameshift_variant,non_coding_transcript_variant,intron_variant
                            Validated:
                            by frequency
                            MAF:
                            -=0.000008/2 (GnomAD_exomes)
                            HGVS:
                            NC_000001.11:g.157767431del, NC_000001.10:g.157737221del, XM_011509974.4:c.962del, XM_011509974.3:c.962del, XM_011509974.2:c.962del, XM_011509974.1:c.962del, NM_030764.4:c.962del, NM_030764.3:c.962del, XM_011509975.4:c.962del, XM_011509975.3:c.962del, XM_011509975.2:c.962del, XM_011509975.1:c.962del, XM_006711535.4:c.931del, XM_006711535.3:c.931del, XM_006711535.2:c.931del, XM_006711535.1:c.931del, XM_011509976.3:c.962del, XM_011509976.2:c.962del, XM_011509976.1:c.962del, XM_017002316.2:c.962del, XM_017002316.1:c.962del, NM_001159488.2:c.962del, NM_001159488.1:c.962del, XM_017002319.2:c.677del, XM_017002319.1:c.677del, XR_001737403.2:n.1164del, XR_001737403.1:n.1503del, XR_001737404.2:n.1133del, XR_001737404.1:n.1472del, XM_047430273.1:c.677del, NM_138739.1:c.203del, XP_011508276.1:p.Cys321fs, NP_110391.2:p.Cys321fs, XP_011508277.1:p.Cys321fs, XP_006711598.1:p.Thr310_Val311insTer, XP_011508278.1:p.Cys321fs, XP_016857805.1:p.Cys321fs, NP_001152960.1:p.Cys321fs, XP_016857808.1:p.Cys226fs, XP_047286229.1:p.Cys226fs

                            14.

                            rs1469499419 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C [Show Flanks]
                              Chromosome:
                              1:157769878 (GRCh38)
                              1:157739668 (GRCh37)
                              Canonical SPDI:
                              NC_000001.11:157769877:T:C
                              Gene:
                              FCRL2 (Varview)
                              Functional Consequence:
                              missense_variant,coding_sequence_variant,non_coding_transcript_variant,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:
                              NC_000001.11:g.157769878T>C, NC_000001.10:g.157739668T>C, NG_082207.1:g.364T>C, XM_011509974.4:c.583A>G, XM_011509974.3:c.583A>G, XM_011509974.2:c.583A>G, XM_011509974.1:c.583A>G, NM_030764.4:c.583A>G, NM_030764.3:c.583A>G, XM_011509975.4:c.583A>G, XM_011509975.3:c.583A>G, XM_011509975.2:c.583A>G, XM_011509975.1:c.583A>G, XM_006711535.4:c.583A>G, XM_006711535.3:c.583A>G, XM_006711535.2:c.583A>G, XM_006711535.1:c.583A>G, XM_011509976.3:c.583A>G, XM_011509976.2:c.583A>G, XM_011509976.1:c.583A>G, XM_017002316.2:c.583A>G, XM_017002316.1:c.583A>G, NM_001159488.2:c.583A>G, NM_001159488.1:c.583A>G, XM_017002317.2:c.583A>G, XM_017002317.1:c.583A>G, XM_017002318.2:c.583A>G, XM_017002318.1:c.583A>G, XR_001737403.2:n.642A>G, XR_001737403.1:n.981A>G, XR_001737404.2:n.642A>G, XR_001737404.1:n.981A>G, XM_047430270.1:c.583A>G, XP_011508276.1:p.Ile195Val, NP_110391.2:p.Ile195Val, XP_011508277.1:p.Ile195Val, XP_006711598.1:p.Ile195Val, XP_011508278.1:p.Ile195Val, XP_016857805.1:p.Ile195Val, NP_001152960.1:p.Ile195Val, XP_016857806.1:p.Ile195Val, XP_016857807.1:p.Ile195Val, XP_047286226.1:p.Ile195Val

                              15.

                              rs1468789541 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>A [Show Flanks]
                                Chromosome:
                                1:157770460 (GRCh38)
                                1:157740250 (GRCh37)
                                Canonical SPDI:
                                NC_000001.11:157770459:G:A
                                Gene:
                                FCRL2 (Varview)
                                Functional Consequence:
                                coding_sequence_variant,non_coding_transcript_variant,stop_gained
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                A=0./0 (ALFA)
                                A=0.000004/1 (TOPMED)
                                A=0.000008/2 (GnomAD_exomes)
                                HGVS:
                                NC_000001.11:g.157770460G>A, NC_000001.10:g.157740250G>A, NG_082207.1:g.946G>A, XM_011509974.4:c.259C>T, XM_011509974.3:c.259C>T, XM_011509974.2:c.259C>T, XM_011509974.1:c.259C>T, NM_030764.4:c.259C>T, NM_030764.3:c.259C>T, XM_011509975.4:c.259C>T, XM_011509975.3:c.259C>T, XM_011509975.2:c.259C>T, XM_011509975.1:c.259C>T, XM_006711535.4:c.259C>T, XM_006711535.3:c.259C>T, XM_006711535.2:c.259C>T, XM_006711535.1:c.259C>T, XM_011509976.3:c.259C>T, XM_011509976.2:c.259C>T, XM_011509976.1:c.259C>T, XM_017002316.2:c.259C>T, XM_017002316.1:c.259C>T, NM_001159488.2:c.259C>T, NM_001159488.1:c.259C>T, XM_017002317.2:c.259C>T, XM_017002317.1:c.259C>T, XM_017002318.2:c.259C>T, XM_017002318.1:c.259C>T, XM_017002319.2:c.259C>T, XM_017002319.1:c.259C>T, NR_125358.2:n.318C>T, NR_125358.1:n.318C>T, XR_001737403.2:n.318C>T, XR_001737403.1:n.657C>T, XR_001737404.2:n.318C>T, XR_001737404.1:n.657C>T, XM_047430270.1:c.259C>T, XM_047430273.1:c.259C>T, XM_047430275.1:c.259C>T, XP_011508276.1:p.Gln87Ter, NP_110391.2:p.Gln87Ter, XP_011508277.1:p.Gln87Ter, XP_006711598.1:p.Gln87Ter, XP_011508278.1:p.Gln87Ter, XP_016857805.1:p.Gln87Ter, NP_001152960.1:p.Gln87Ter, XP_016857806.1:p.Gln87Ter, XP_016857807.1:p.Gln87Ter, XP_016857808.1:p.Gln87Ter, XP_047286226.1:p.Gln87Ter, XP_047286229.1:p.Gln87Ter, XP_047286231.1:p.Gln87Ter

                                16.

                                rs1468228115 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  G>- [Show Flanks]
                                  Chromosome:
                                  1:157770112 (GRCh38)
                                  1:157739902 (GRCh37)
                                  Canonical SPDI:
                                  NC_000001.11:157770111:GG:G
                                  Gene:
                                  FCRL2 (Varview)
                                  Functional Consequence:
                                  frameshift_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  GG=0./0 (ALFA)
                                  -=0.000007/1 (GnomAD)
                                  -=0.000008/2 (TOPMED)
                                  HGVS:
                                  NC_000001.11:g.157770113del, NC_000001.10:g.157739903del, NG_082207.1:g.599del, XM_011509974.4:c.349del, XM_011509974.3:c.349del, XM_011509974.2:c.349del, XM_011509974.1:c.349del, NM_030764.4:c.349del, NM_030764.3:c.349del, XM_011509975.4:c.349del, XM_011509975.3:c.349del, XM_011509975.2:c.349del, XM_011509975.1:c.349del, XM_006711535.4:c.349del, XM_006711535.3:c.349del, XM_006711535.2:c.349del, XM_006711535.1:c.349del, XM_011509976.3:c.349del, XM_011509976.2:c.349del, XM_011509976.1:c.349del, XM_017002316.2:c.349del, XM_017002316.1:c.349del, NM_001159488.2:c.349del, NM_001159488.1:c.349del, XM_017002317.2:c.349del, XM_017002317.1:c.349del, XM_017002318.2:c.349del, XM_017002318.1:c.349del, XR_001737403.2:n.408del, XR_001737403.1:n.747del, XR_001737404.2:n.408del, XR_001737404.1:n.747del, XM_047430270.1:c.349del, XP_011508276.1:p.Gln117fs, NP_110391.2:p.Gln117fs, XP_011508277.1:p.Gln117fs, XP_006711598.1:p.Gln117fs, XP_011508278.1:p.Gln117fs, XP_016857805.1:p.Gln117fs, NP_001152960.1:p.Gln117fs, XP_016857806.1:p.Gln117fs, XP_016857807.1:p.Gln117fs, XP_047286226.1:p.Gln117fs

                                  17.

                                  rs1467281793 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A [Show Flanks]
                                    Chromosome:
                                    1:157770468 (GRCh38)
                                    1:157740258 (GRCh37)
                                    Canonical SPDI:
                                    NC_000001.11:157770467:G:A
                                    Gene:
                                    FCRL2 (Varview)
                                    Functional Consequence:
                                    missense_variant,coding_sequence_variant,non_coding_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    A=0./0 (ALFA)
                                    A=0.000004/1 (TOPMED)
                                    A=0.000007/1 (GnomAD)
                                    HGVS:
                                    NC_000001.11:g.157770468G>A, NC_000001.10:g.157740258G>A, NG_082207.1:g.954G>A, XM_011509974.4:c.251C>T, XM_011509974.3:c.251C>T, XM_011509974.2:c.251C>T, XM_011509974.1:c.251C>T, NM_030764.4:c.251C>T, NM_030764.3:c.251C>T, XM_011509975.4:c.251C>T, XM_011509975.3:c.251C>T, XM_011509975.2:c.251C>T, XM_011509975.1:c.251C>T, XM_006711535.4:c.251C>T, XM_006711535.3:c.251C>T, XM_006711535.2:c.251C>T, XM_006711535.1:c.251C>T, XM_011509976.3:c.251C>T, XM_011509976.2:c.251C>T, XM_011509976.1:c.251C>T, XM_017002316.2:c.251C>T, XM_017002316.1:c.251C>T, NM_001159488.2:c.251C>T, NM_001159488.1:c.251C>T, XM_017002317.2:c.251C>T, XM_017002317.1:c.251C>T, XM_017002318.2:c.251C>T, XM_017002318.1:c.251C>T, XM_017002319.2:c.251C>T, XM_017002319.1:c.251C>T, NR_125358.2:n.310C>T, NR_125358.1:n.310C>T, XR_001737403.2:n.310C>T, XR_001737403.1:n.649C>T, XR_001737404.2:n.310C>T, XR_001737404.1:n.649C>T, XM_047430270.1:c.251C>T, XM_047430273.1:c.251C>T, XM_047430275.1:c.251C>T, XP_011508276.1:p.Thr84Ile, NP_110391.2:p.Thr84Ile, XP_011508277.1:p.Thr84Ile, XP_006711598.1:p.Thr84Ile, XP_011508278.1:p.Thr84Ile, XP_016857805.1:p.Thr84Ile, NP_001152960.1:p.Thr84Ile, XP_016857806.1:p.Thr84Ile, XP_016857807.1:p.Thr84Ile, XP_016857808.1:p.Thr84Ile, XP_047286226.1:p.Thr84Ile, XP_047286229.1:p.Thr84Ile, XP_047286231.1:p.Thr84Ile

                                    18.

                                    rs1466586712 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>G [Show Flanks]
                                      Chromosome:
                                      1:157770056 (GRCh38)
                                      1:157739846 (GRCh37)
                                      Canonical SPDI:
                                      NC_000001.11:157770055:C:G
                                      Gene:
                                      FCRL2 (Varview)
                                      Functional Consequence:
                                      non_coding_transcript_variant,missense_variant,coding_sequence_variant,intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      G=0./0 (ALFA)
                                      G=0.000004/1 (GnomAD_exomes)
                                      G=0.000007/1 (GnomAD)
                                      HGVS:
                                      NC_000001.11:g.157770056C>G, NC_000001.10:g.157739846C>G, NG_082207.1:g.542C>G, XM_011509974.4:c.405G>C, XM_011509974.3:c.405G>C, XM_011509974.2:c.405G>C, XM_011509974.1:c.405G>C, NM_030764.4:c.405G>C, NM_030764.3:c.405G>C, XM_011509975.4:c.405G>C, XM_011509975.3:c.405G>C, XM_011509975.2:c.405G>C, XM_011509975.1:c.405G>C, XM_006711535.4:c.405G>C, XM_006711535.3:c.405G>C, XM_006711535.2:c.405G>C, XM_006711535.1:c.405G>C, XM_011509976.3:c.405G>C, XM_011509976.2:c.405G>C, XM_011509976.1:c.405G>C, XM_017002316.2:c.405G>C, XM_017002316.1:c.405G>C, NM_001159488.2:c.405G>C, NM_001159488.1:c.405G>C, XM_017002317.2:c.405G>C, XM_017002317.1:c.405G>C, XM_017002318.2:c.405G>C, XM_017002318.1:c.405G>C, XR_001737403.2:n.464G>C, XR_001737403.1:n.803G>C, XR_001737404.2:n.464G>C, XR_001737404.1:n.803G>C, XM_047430270.1:c.405G>C, XP_011508276.1:p.Gln135His, NP_110391.2:p.Gln135His, XP_011508277.1:p.Gln135His, XP_006711598.1:p.Gln135His, XP_011508278.1:p.Gln135His, XP_016857805.1:p.Gln135His, NP_001152960.1:p.Gln135His, XP_016857806.1:p.Gln135His, XP_016857807.1:p.Gln135His, XP_047286226.1:p.Gln135His

                                      19.

                                      rs1465276241 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>T [Show Flanks]
                                        Chromosome:
                                        1:157768512 (GRCh38)
                                        1:157738302 (GRCh37)
                                        Canonical SPDI:
                                        NC_000001.11:157768511:A:T
                                        Gene:
                                        FCRL2 (Varview)
                                        Functional Consequence:
                                        non_coding_transcript_variant,missense_variant,coding_sequence_variant,intron_variant
                                        Validated:
                                        by frequency
                                        MAF:
                                        T=0.000004/1 (GnomAD_exomes)
                                        HGVS:
                                        NC_000001.11:g.157768512A>T, NC_000001.10:g.157738302A>T, XM_011509974.4:c.785T>A, XM_011509974.3:c.785T>A, XM_011509974.2:c.785T>A, XM_011509974.1:c.785T>A, NM_030764.4:c.785T>A, NM_030764.3:c.785T>A, XM_011509975.4:c.785T>A, XM_011509975.3:c.785T>A, XM_011509975.2:c.785T>A, XM_011509975.1:c.785T>A, XM_006711535.4:c.785T>A, XM_006711535.3:c.785T>A, XM_006711535.2:c.785T>A, XM_006711535.1:c.785T>A, XM_011509976.3:c.785T>A, XM_011509976.2:c.785T>A, XM_011509976.1:c.785T>A, XM_017002316.2:c.785T>A, XM_017002316.1:c.785T>A, NM_001159488.2:c.785T>A, NM_001159488.1:c.785T>A, XM_017002317.2:c.785T>A, XM_017002317.1:c.785T>A, XM_017002318.2:c.785T>A, XM_017002318.1:c.785T>A, XM_017002319.2:c.500T>A, XM_017002319.1:c.500T>A, XR_001737403.2:n.844T>A, XR_001737403.1:n.1183T>A, XR_001737404.2:n.844T>A, XR_001737404.1:n.1183T>A, XM_047430270.1:c.785T>A, XM_047430273.1:c.500T>A, XM_047430275.1:c.500T>A, XP_011508276.1:p.Ile262Asn, NP_110391.2:p.Ile262Asn, XP_011508277.1:p.Ile262Asn, XP_006711598.1:p.Ile262Asn, XP_011508278.1:p.Ile262Asn, XP_016857805.1:p.Ile262Asn, NP_001152960.1:p.Ile262Asn, XP_016857806.1:p.Ile262Asn, XP_016857807.1:p.Ile262Asn, XP_016857808.1:p.Ile167Asn, XP_047286226.1:p.Ile262Asn, XP_047286229.1:p.Ile167Asn, XP_047286231.1:p.Ile167Asn

                                        20.

                                        rs1463876629 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          1:157770644 (GRCh38)
                                          1:157740434 (GRCh37)
                                          Canonical SPDI:
                                          NC_000001.11:157770643:G:A
                                          Gene:
                                          FCRL2 (Varview)
                                          Functional Consequence:
                                          synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          A=0./0 (ALFA)
                                          A=0.000004/1 (TOPMED)
                                          A=0.000007/1 (GnomAD)
                                          HGVS:
                                          NC_000001.11:g.157770644G>A, NC_000001.10:g.157740434G>A, NG_082207.1:g.1130G>A, XM_011509974.4:c.75C>T, XM_011509974.3:c.75C>T, XM_011509974.2:c.75C>T, XM_011509974.1:c.75C>T, NM_030764.4:c.75C>T, NM_030764.3:c.75C>T, XM_011509975.4:c.75C>T, XM_011509975.3:c.75C>T, XM_011509975.2:c.75C>T, XM_011509975.1:c.75C>T, XM_006711535.4:c.75C>T, XM_006711535.3:c.75C>T, XM_006711535.2:c.75C>T, XM_006711535.1:c.75C>T, XM_011509976.3:c.75C>T, XM_011509976.2:c.75C>T, XM_011509976.1:c.75C>T, XM_017002316.2:c.75C>T, XM_017002316.1:c.75C>T, NM_001159488.2:c.75C>T, NM_001159488.1:c.75C>T, XM_017002317.2:c.75C>T, XM_017002317.1:c.75C>T, XM_017002318.2:c.75C>T, XM_017002318.1:c.75C>T, XM_017002319.2:c.75C>T, XM_017002319.1:c.75C>T, NR_125358.2:n.134C>T, NR_125358.1:n.134C>T, XR_001737403.2:n.134C>T, XR_001737403.1:n.473C>T, XR_001737404.2:n.134C>T, XR_001737404.1:n.473C>T, XM_047430270.1:c.75C>T, XM_047430273.1:c.75C>T, XM_047430275.1:c.75C>T

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