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项目:第1至20项,共964项

1

1490746115卢比[智人]
    变量类型:
    SNV公司
    等位基因:
    G> A、T[展示侧翼]
    染色体:
    10:102399642(GRCh38)
    10:104159399(GRCh37)
    标准SPDI:
    NC_000010.11:102399641:G:A,NC_00000.11:10239941:G:T
    基因:
    NFKB2型(Varview公司)
    功能后果:
    编码序列变量,错义变量
    已验证:
    按频率、按alfa、按簇
    最大允许流量:
    T=0./0(ALFA公司)
    T=0.000004/1(顶部)
    A=0.000008/1(GnomAD_exomes)
    HGVS:
    NC_000010.11:g.102399642G>A,NC_000010.11:g.102399642G>T,NC_000010.10:g.104159399G>A,NC_000010.10:g.104159399G>T,NG_033874.2:g.10533G>A,NG_033874.2:g.10533G>T,NM_002502.6:c.1393G>A,NM_002502.6:c.1393G>T,NM_002502.5:c.1393G>A,NM_002502.5:c.1393G>T,NM_002502.4:c.1393G>A,NM_002502.4:c.1393G>T,NM_001077494.3:c.1393G>A,NM_001077494.3:c.1393G>T,NM_001077494.2:c.1393G>A,NM_001077494.2:c.1393G>T,NM_001261403.3:c.1393G>A,NM_001261403.3:c.1393G>T,NM_001261403.2:c.1393G>A,NM_001261403.2:c.1393G>T,NM_001261403.1:c.1393G>A,NM_001261403.1:c.1393G>T,NM_001322934.2:c.1393G>A,NM_001322934.2:c.1393G>T,NM_001322934.1:c.1393G>A,NM_001322934.1:c.1393G>T,NM_001288724.1:c.1393G>A,NM_001288724.1:c.1393G>T,NM_001322935.1:c.1267G>A,NM_001322935.1:c.1267G>T,NR_048560.1:n.1956G>A,NR_048560.1:n.1956G>T,NM_001077493.1:c.1393G>A,NM_001077493.1:c.1393G>T,NP_002493.3:p.Gly465Ser,NP_002493.3:p.Gly465Cys,NP_001070962.1:p.Gly465Ser,NP_001070962.1:p.格雷465Cys,NP_001248332.1:p.Gly465Ser公司,NP_001248332.1:p.Gly465Cys公司,NP_001309863.1:p.Gly465Ser公司,NP_001309863.1:p.Gly465Cys公司,NP_001275653.1:p.Gly465Ser公司,NP_001275653.1:p.Gly465Cys公司,NP_001309864.1:p.Gly423Ser,NP_001309864.1:p.Gly423Cys
    4

    rs1488705625[智人]
      变量类型:
      SNV公司
      等位基因:
      G> A类[展示侧翼]
      染色体:
      10:102401869(GRCh38)
      10:104161626(GRCh37)
      标准SPDI:
      NC_000010.11:102401868:G:A
      基因:
      NFKB2型(Varview公司)
      功能后果:
      同义词变体,编码序列变体
      临床意义:
      可能发生
      已验证:
      按频率、按alfa、按簇
      最大允许流量:
      A=0./0(ALFA公司)
      A=0.000004/1(GnomAD_exomes)
      A=0.000004/1(顶部)
      A=0.000007/1(GnomAD)
      HGVS:
      5

      rs1486109142[智人]
        变量类型:
        SNV公司
        等位基因:
        C> A、T[展示侧翼]
        染色体:
        10:102394119(GRCh38)
        10:104153876(GRCh37)
        标准SPDI:
        NC_000010.11:102394118:C:A,NC_00000.11:1023941018:C:T
        基因:
        NFKB2型(Varview公司)
        功能后果:
        5_prime_UTR_变量,genic_upstream_transcript_variant,upstream _transcript_变量
        已验证:
        按频率、按alfa、按簇
        最大允许流量:
        T=0./0(ALFA公司)
        T=0.000007/1(GnomAD)
        T=0.000015/4(顶部)
        HGVS:
        9

        1483460853卢比[智人]
          变量类型:
          SNV公司
          等位基因:
          G> A、T[展示侧翼]
          染色体:
          10:102394490(GRCh38)
          10:104154247(GRCh37)
          标准SPDI:
          NC_000010.11:102394489:G:A,NC_00000.11:10239489:G:T
          基因:
          NFKB2型(Varview公司)
          功能后果:
          5_prime_UTR_variant、geni_upstream_transcript_variant、upstream_transcript_variant
          已验证:
          按频率,按alfa
          最大允许流量:
          T=0./0(ALFA公司)
          A=0.000019/5(顶部)
          HGVS:
          13

          rs1479584792公司[智人]
            变量类型:
            SNV公司
            等位基因:
            C> G、T[展示侧翼]
            染色体:
            10:102399438(GRCh38)
            10:104159195(GRCh37)
            标准SPDI:
            NC_000010.11:102399437:C:G,NC_00000.11:1023994 37:C:T
            基因:
            NFKB2型(Varview公司)
            功能后果:
            错义变量,编码_序列变量
            已验证:
            按频率、按alfa、按簇
            最大允许流量:
            G=0./0(ALFA公司)
            G=0.000008/2(顶部)
            HGVS:
            NC_000010.11:g.102399438C>g,NC_000010.11:g.102399438C>T,NC_000010.10:g.104159195C>g,NC_000010.10:g.104159195C>T,NG_033874.2:g.10329C>g,NG_033874.2:g.10329C>T,NM_002502.6:c.1268C>G,NM_002502.6:c.1268C>T,NM_002502.5:c.1268C>G,NM_002502.5:c.1268C>T,NM_002502.4:c.1268C>G,NM_002502.4:c.1268C>T,NM_001077494.3:c.1268C>G,NM_001077494.3:c.1268C>T,NM_001077494.2:c.1268C>G,NM_001077494.2:c.1268C>T,NM_001261403.3:c.1268C>G,NM_001261403.3:c.1268C>T,NM_001261403.2:c.1268C>G,NM_001261403.2:c.1268C>T,NM_001261403.1:c.1268C>G,NM_001261403.1:c.1268C>T,NM_001322934.2:c.1268C>G,NM_001322934.2:约1268C>T,NM_001322934.1:c.1268C>G,NM_001322934.1:c.1268C>T,NM_001288724.1:c.1268C>G,NM_001288724.1:c.1268C>T,NM_001322935.1:c.1142C>G,NM_001322935.1:c.1142C>T,NR_048560.1:n.1831C>G,NR_048560.1:n.1831C>T,NM_001077493.1:c.1268C>G,NM_001077493.1:c.1268C>T,NP_002493.3:p.Pro423组织,NP_002493.3:p.Pro423Leu,NP_001070962.1:p.Pro423组织,NP_001070962.1:p.Pro423Leu,NP_001248332.1:p.Pro423Arg,NP_001248332.1:p.Pro423Leu,NP_001309863.1:p.Pro423组织,NP_001309863.1:p.Pro423Leu,NP_001275653.1:p.Pro423组织,NP_001275653.1:p.Pro423Leu,NP_001309864.1:p.Pro381Arg,NP_001309864.1:p.Pro381Leu
            14

            1478950154卢比[智人]
              变量类型:
              DELINS公司
              等位基因:
              ->G公司[展示侧翼]
              染色体:
              10:102394486(GRCh38)
              10:104154244(GRCh37)
              标准SPDI:
              NC_000010.11:102394486:GGGGG GGG
              基因:
              NFKB2型(Varview公司)
              功能后果:
              5_prime_UTR_变量,genic_upstream_transcript_variant,upstream _transcript_变量
              已验证:
              按频率、按alfa、按簇
              最大允许流量:
              GGGGG=0./0(ALFA公司)
              G=0.000023/6(顶部)
              G=0.000029/4(GnomAD)
              G=0.000548/1(韩国1K)
              HGVS:
              18

              1477526947卢比[智人]
                变量类型:
                SNV公司
                等位基因:
                G> A类[展示侧翼]
                染色体:
                10:102400994(GRCh38)
                10:104160751(GRCh37)
                标准SPDI:
                NC_000010.11:102400993:G:A号机组
                基因:
                NFKB2型(Varview公司)
                功能后果:
                同义词变体,编码序列变体
                已验证:
                按频率
                最大允许流量:
                A=0.000008/2(GnomAD_exomes)
                HGVS:
                20

                1477050280卢比[智人]
                  变量类型:
                  SNV公司
                  等位基因:
                  A> G公司[展示侧翼]
                  染色体:
                  10:102398456(GRCh38)
                  10:104158213(GRCh37)
                  标准SPDI:
                  NC_000010.11:102398455:答:G
                  基因:
                  NFKB2型(Varview公司)
                  功能后果:
                  同义变量,编码序列变量
                  临床意义:
                  不确定重要性
                  已验证:
                  按频率、按alfa、按簇
                  最大允许流量:
                  G=0./0(ALFA公司)
                  G=0.000007/1(GnomAD)
                  G=0.000011/3(顶部)
                  HGVS:

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