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Items: 1 to 20 of 230

1.

rs1484707199 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>A [Show Flanks]
    Chromosome:
    8:70574967 (GRCh38)
    8:71487202 (GRCh37)
    Canonical SPDI:
    NC_000008.11:70574966:C:A
    Gene:
    TRAM1 (Varview)
    Functional Consequence:
    missense_variant,coding_sequence_variant
    Validated:
    by frequency
    MAF:
    A=0.000004/1 (GnomAD_exomes)
    HGVS:
    2.

    rs1481131442 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>G [Show Flanks]
      Chromosome:
      8:70583684 (GRCh38)
      8:71495919 (GRCh37)
      Canonical SPDI:
      NC_000008.11:70583683:A:G
      Gene:
      TRAM1 (Varview)
      Functional Consequence:
      missense_variant,coding_sequence_variant
      Validated:
      by frequency
      MAF:
      G=0.000004/1 (GnomAD_exomes)
      HGVS:
      3.

      rs1474372322 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>T [Show Flanks]
        Chromosome:
        8:70583254 (GRCh38)
        8:71495489 (GRCh37)
        Canonical SPDI:
        NC_000008.11:70583253:G:T
        Gene:
        TRAM1 (Varview)
        Functional Consequence:
        synonymous_variant,coding_sequence_variant
        Validated:
        by frequency
        MAF:
        T=0.000004/1 (GnomAD_exomes)
        HGVS:
        4.

        rs1472415062 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>T [Show Flanks]
          Chromosome:
          8:70594513 (GRCh38)
          8:71506748 (GRCh37)
          Canonical SPDI:
          NC_000008.11:70594512:G:T
          Gene:
          TRAM1 (Varview)
          Functional Consequence:
          coding_sequence_variant,missense_variant
          Validated:
          by frequency,by alfa
          MAF:
          T=0./0 (ALFA)
          HGVS:
          5.

          rs1466619053 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>A [Show Flanks]
            Chromosome:
            8:70574944 (GRCh38)
            8:71487179 (GRCh37)
            Canonical SPDI:
            NC_000008.11:70574943:C:A
            Gene:
            TRAM1 (Varview)
            Functional Consequence:
            coding_sequence_variant,missense_variant
            Validated:
            by frequency
            MAF:
            A=0.000004/1 (GnomAD_exomes)
            HGVS:
            6.

            rs1465466324 [Homo sapiens]
              Variant type:
              DEL
              Alleles:
              TAACACATTGA>- [Show Flanks]
              Chromosome:
              8:70583658 (GRCh38)
              8:71495893 (GRCh37)
              Canonical SPDI:
              NC_000008.11:70583657:TAACACATTGA:
              Gene:
              TRAM1 (Varview)
              Functional Consequence:
              coding_sequence_variant,frameshift_variant
              Validated:
              by frequency
              MAF:
              -=0.000004/1 (GnomAD_exomes)
              HGVS:
              8.

              rs1451579412 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                A>G [Show Flanks]
                Chromosome:
                8:70583676 (GRCh38)
                8:71495911 (GRCh37)
                Canonical SPDI:
                NC_000008.11:70583675:A:G
                Gene:
                TRAM1 (Varview)
                Functional Consequence:
                coding_sequence_variant,synonymous_variant
                Validated:
                by frequency
                MAF:
                G=0.000004/1 (GnomAD_exomes)
                HGVS:
                9.

                rs1450006404 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>T [Show Flanks]
                  Chromosome:
                  8:70583249 (GRCh38)
                  8:71495484 (GRCh37)
                  Canonical SPDI:
                  NC_000008.11:70583248:C:T
                  Gene:
                  TRAM1 (Varview)
                  Functional Consequence:
                  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:
                  10.

                  rs1445433300 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    T>C [Show Flanks]
                    Chromosome:
                    8:70583309 (GRCh38)
                    8:71495544 (GRCh37)
                    Canonical SPDI:
                    NC_000008.11:70583308:T:C
                    Gene:
                    TRAM1 (Varview)
                    Functional Consequence:
                    coding_sequence_variant,synonymous_variant
                    Validated:
                    by frequency
                    MAF:
                    C=0.000004/1 (GnomAD_exomes)
                    HGVS:
                    11.

                    rs1427619265 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      A>G [Show Flanks]
                      Chromosome:
                      8:70598006 (GRCh38)
                      8:71510241 (GRCh37)
                      Canonical SPDI:
                      NC_000008.11:70598005:A:G
                      Gene:
                      TRAM1 (Varview)
                      Functional Consequence:
                      coding_sequence_variant,synonymous_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      G=0./0 (ALFA)
                      G=0.000004/1 (TOPMED)
                      G=0.000007/1 (GnomAD)
                      HGVS:
                      12.

                      rs1424388393 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        A>G [Show Flanks]
                        Chromosome:
                        8:70574996 (GRCh38)
                        8:71487231 (GRCh37)
                        Canonical SPDI:
                        NC_000008.11:70574995:A:G
                        Gene:
                        TRAM1 (Varview)
                        Functional Consequence:
                        coding_sequence_variant,missense_variant
                        Validated:
                        by frequency
                        MAF:
                        G=0.000004/1 (GnomAD_exomes)
                        HGVS:
                        13.

                        rs1412074177 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A [Show Flanks]
                          Chromosome:
                          8:70587167 (GRCh38)
                          8:71499402 (GRCh37)
                          Canonical SPDI:
                          NC_000008.11:70587166:G:A
                          Gene:
                          TRAM1 (Varview)
                          Functional Consequence:
                          missense_variant,coding_sequence_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          A=0./0 (ALFA)
                          A=0.000004/1 (TOPMED)
                          HGVS:
                          14.

                          rs1410791448 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>G [Show Flanks]
                            Chromosome:
                            8:70583701 (GRCh38)
                            8:71495936 (GRCh37)
                            Canonical SPDI:
                            NC_000008.11:70583700:T:G
                            Gene:
                            TRAM1 (Varview)
                            Functional Consequence:
                            missense_variant,coding_sequence_variant
                            Validated:
                            by frequency
                            MAF:
                            G=0.000004/1 (GnomAD_exomes)
                            HGVS:
                            15.

                            rs1407434609 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              A>T [Show Flanks]
                              Chromosome:
                              8:70583286 (GRCh38)
                              8:71495521 (GRCh37)
                              Canonical SPDI:
                              NC_000008.11:70583285:A:T
                              Gene:
                              TRAM1 (Varview)
                              Functional Consequence:
                              missense_variant,coding_sequence_variant
                              Validated:
                              by frequency
                              MAF:
                              T=0.000004/1 (GnomAD_exomes)
                              HGVS:
                              16.

                              rs1405540802 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                8:70598134 (GRCh38)
                                8:71510369 (GRCh37)
                                Canonical SPDI:
                                NC_000008.11:70598133:A:G
                                Gene:
                                TRAM1 (Varview)
                                Functional Consequence:
                                synonymous_variant,coding_sequence_variant
                                Validated:
                                by frequency
                                MAF:
                                G=0.000004/1 (GnomAD_exomes)
                                HGVS:
                                17.

                                rs1403005500 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  A>G [Show Flanks]
                                  Chromosome:
                                  8:70594545 (GRCh38)
                                  8:71506780 (GRCh37)
                                  Canonical SPDI:
                                  NC_000008.11:70594544:A:G
                                  Gene:
                                  TRAM1 (Varview)
                                  Functional Consequence:
                                  synonymous_variant,coding_sequence_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  G=0./0 (ALFA)
                                  G=0.000004/1 (TOPMED)
                                  G=0.000014/2 (GnomAD)
                                  HGVS:
                                  18.

                                  rs1396787315 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A [Show Flanks]
                                    Chromosome:
                                    8:70586930 (GRCh38)
                                    8:71499165 (GRCh37)
                                    Canonical SPDI:
                                    NC_000008.11:70586929:G:A
                                    Gene:
                                    TRAM1 (Varview)
                                    Functional Consequence:
                                    synonymous_variant,coding_sequence_variant
                                    Validated:
                                    by frequency
                                    MAF:
                                    A=0.000004/1 (GnomAD_exomes)
                                    HGVS:
                                    19.

                                    rs1391302733 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>A [Show Flanks]
                                      Chromosome:
                                      8:70597993 (GRCh38)
                                      8:71510228 (GRCh37)
                                      Canonical SPDI:
                                      NC_000008.11:70597992:G:A
                                      Gene:
                                      TRAM1 (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,missense_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      A=0./0 (ALFA)
                                      HGVS:
                                      20.

                                      rs1387844927 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        8:70583194 (GRCh38)
                                        8:71495429 (GRCh37)
                                        Canonical SPDI:
                                        NC_000008.11:70583193:T:C
                                        Gene:
                                        TRAM1 (Varview)
                                        Functional Consequence:
                                        missense_variant,coding_sequence_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        C=0./0 (ALFA)
                                        C=0.000008/2 (TOPMED)
                                        C=0.000014/2 (GnomAD)
                                        HGVS:

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