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Items: 1 to 20 of 572

1.

rs1490447456 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    19:54664424 (GRCh38)
    19:55175875 (GRCh37)
    Canonical SPDI:
    NC_000019.10:54664423:A:G
    Gene:
    LILRB4 (Varview)
    Functional Consequence:
    synonymous_variant,coding_sequence_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0./0 (ALFA)
    G=0.000004/1 (GnomAD_exomes)
    G=0.000004/1 (TOPMED)
    G=0.000007/1 (GnomAD)
    HGVS:
    NC_000019.10:g.54664424A>G, NW_004166865.1:g.638791A>G, NW_003571061.2:g.390928A>G, NW_003571061.1:g.390927A>G, NT_187693.1:g.646989A>G, NC_000019.9:g.55175875A>G, NW_003571060.1:g.569306A>G, NW_003571054.1:g.570827A>G, NM_001278428.4:c.594A>G, NM_001278428.3:c.594A>G, NM_001278428.2:c.594A>G, NM_001278426.4:c.594A>G, NM_001278426.3:c.594A>G, NM_001278426.2:c.594A>G, NM_001278427.4:c.594A>G, NM_001278427.3:c.594A>G, NM_001278427.2:c.594A>G, NM_001278429.4:c.558A>G, NM_001278429.3:c.681A>G, NM_001278429.2:c.681A>G, NM_001278430.4:c.594A>G, NM_001278430.3:c.594A>G, NM_001278430.2:c.594A>G, NM_006847.3:c.594A>G, XM_017026216.2:c.594A>G, XM_017026216.1:c.717A>G, NM_006847.2:c.594A>G, NM_001394933.1:c.594A>G, NM_001394934.1:c.594A>G, XM_047438100.1:c.558A>G, NM_001394937.1:c.558A>G, XM_047438101.1:c.558A>G, NM_001394938.1:c.558A>G, NM_001394935.1:c.594A>G, NM_001394936.1:c.558A>G, NM_006847.1:c.594A>G, NM_001394939.1:c.594A>G, XM_047438102.1:c.594A>G, NM_001081438.1:c.594A>G, XM_047438103.1:c.333A>G

    2.

    rs1490396409 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ->TCAC [Show Flanks]
      Chromosome:
      19:54663785 (GRCh38)
      19:55175244 (GRCh37)
      Canonical SPDI:
      NC_000019.10:54663785:C:CTCAC
      Gene:
      LILRB4 (Varview)
      Functional Consequence:
      frameshift_variant,intron_variant,coding_sequence_variant
      Validated:
      by frequency
      MAF:
      CTCA=0.000004/1 (GnomAD_exomes)
      HGVS:
      NC_000019.10:g.54663786_54663787insTCAC, NW_004166865.1:g.638153_638154insTCAC, NW_003571061.2:g.390290_390291insTCAC, NW_003571061.1:g.390289_390290insTCAC, NT_187693.1:g.646358_646359insTCAC, NC_000019.9:g.55175244_55175245insTCAC, NW_003571060.1:g.568668_568669insTCAC, NW_003571054.1:g.570189_570190insTCAC, NM_001278428.4:c.103_104insTCAC, NM_001278428.3:c.103_104insTCAC, NM_001278428.2:c.103_104insTCAC, NM_001278426.4:c.103_104insTCAC, NM_001278426.3:c.103_104insTCAC, NM_001278426.2:c.103_104insTCAC, NM_001278427.4:c.103_104insTCAC, NM_001278427.3:c.103_104insTCAC, NM_001278427.2:c.103_104insTCAC, NM_001278429.4:c.67_68insTCAC, NM_001278429.3:c.190_191insTCAC, NM_001278429.2:c.190_191insTCAC, NM_001278430.4:c.103_104insTCAC, NM_001278430.3:c.103_104insTCAC, NM_001278430.2:c.103_104insTCAC, NM_006847.3:c.103_104insTCAC, NM_006847.2:c.103_104insTCAC, XM_017026216.2:c.103_104insTCAC, XM_017026216.1:c.226_227insTCAC, NM_001394934.1:c.103_104insTCAC, XM_047438100.1:c.67_68insTCAC, NM_001394937.1:c.67_68insTCAC, XM_047438101.1:c.67_68insTCAC, NM_001394938.1:c.67_68insTCAC, NM_001394939.1:c.103_104insTCAC, NM_001081438.1:c.103_104insTCAC, NM_001394933.1:c.103_104insTCAC, NM_001394936.1:c.67_68insTCAC, NM_006847.1:c.103_104insTCAC, XM_047438102.1:c.103_104insTCAC, NM_001394935.1:c.103_104insTCAC, NP_001265357.2:p.Pro35fs, NP_001265355.2:p.Pro35fs, NP_001265356.2:p.Pro35fs, NP_001265358.3:p.Pro23fs, NP_001265359.2:p.Pro35fs, XP_016881705.2:p.Pro35fs, NP_001381863.1:p.Pro35fs, XP_047294056.1:p.Pro23fs, NP_001381866.1:p.Pro23fs, XP_047294057.1:p.Pro23fs, NP_001381867.1:p.Pro23fs, NP_001381868.1:p.Pro35fs, NP_001381862.1:p.Pro35fs, NP_001381865.1:p.Pro23fs, XP_047294058.1:p.Pro35fs, NP_001381864.1:p.Pro35fs

      3.

      rs1489604518 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A [Show Flanks]
        Chromosome:
        19:54663780 (GRCh38)
        19:55175238 (GRCh37)
        Canonical SPDI:
        NC_000019.10:54663779:G:A
        Gene:
        LILRB4 (Varview)
        Functional Consequence:
        missense_variant,intron_variant,coding_sequence_variant
        HGVS:
        NC_000019.10:g.54663780G>A, NW_004166865.1:g.638147G>A, NW_003571061.2:g.390284G>A, NW_003571061.1:g.390283G>A, NT_187693.1:g.646352G>A, NC_000019.9:g.55175238G>A, NW_003571060.1:g.568662G>A, NW_003571054.1:g.570183G>A, NM_001278428.4:c.97G>A, NM_001278428.3:c.97G>A, NM_001278428.2:c.97G>A, NM_001278426.4:c.97G>A, NM_001278426.3:c.97G>A, NM_001278426.2:c.97G>A, NM_001278427.4:c.97G>A, NM_001278427.3:c.97G>A, NM_001278427.2:c.97G>A, NM_001278429.4:c.61G>A, NM_001278429.3:c.184G>A, NM_001278429.2:c.184G>A, NM_001278430.4:c.97G>A, NM_001278430.3:c.97G>A, NM_001278430.2:c.97G>A, NM_006847.3:c.97G>A, NM_006847.2:c.97G>A, XM_017026216.2:c.97G>A, XM_017026216.1:c.220G>A, NM_001394934.1:c.97G>A, XM_047438100.1:c.61G>A, NM_001394937.1:c.61G>A, XM_047438101.1:c.61G>A, NM_001394938.1:c.61G>A, NM_001394939.1:c.97G>A, NM_001081438.1:c.97G>A, NM_001394933.1:c.97G>A, NM_001394936.1:c.61G>A, NM_006847.1:c.97G>A, XM_047438102.1:c.97G>A, NM_001394935.1:c.97G>A, NP_001265357.2:p.Ala33Thr, NP_001265355.2:p.Ala33Thr, NP_001265356.2:p.Ala33Thr, NP_001265358.3:p.Ala21Thr, NP_001265359.2:p.Ala33Thr, XP_016881705.2:p.Ala33Thr, NP_001381863.1:p.Ala33Thr, XP_047294056.1:p.Ala21Thr, NP_001381866.1:p.Ala21Thr, XP_047294057.1:p.Ala21Thr, NP_001381867.1:p.Ala21Thr, NP_001381868.1:p.Ala33Thr, NP_001381862.1:p.Ala33Thr, NP_001381865.1:p.Ala21Thr, XP_047294058.1:p.Ala33Thr, NP_001381864.1:p.Ala33Thr

        4.

        rs1486894096 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>A,T [Show Flanks]
          Chromosome:
          19:54667989 (GRCh38)
          19:55179440 (GRCh37)
          Canonical SPDI:
          NC_000019.10:54667988:C:A,NC_000019.10:54667988:C:T
          Gene:
          LILRB4 (Varview)
          Functional Consequence:
          synonymous_variant,genic_downstream_transcript_variant,coding_sequence_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0./0 (ALFA)
          T=0.000004/1 (TOPMED)
          T=0.000007/1 (GnomAD)
          T=0.000008/2 (GnomAD_exomes)
          HGVS:
          NC_000019.10:g.54667989C>A, NC_000019.10:g.54667989C>T, NW_004166865.1:g.642356C>A, NW_004166865.1:g.642356C>T, NW_003571061.2:g.394493C>A, NW_003571061.2:g.394493C>T, NW_003571061.1:g.394492C>A, NW_003571061.1:g.394492C>T, NT_187693.1:g.650554C>A, NT_187693.1:g.650554C>T, NC_000019.9:g.55179440C>A, NC_000019.9:g.55179440C>T, NW_003571060.1:g.572871C>A, NW_003571060.1:g.572871C>T, NW_003571054.1:g.574392C>A, NW_003571054.1:g.574392C>T, NM_001278428.4:c.1317C>A, NM_001278428.4:c.1317C>T, NM_001278428.3:c.1317C>A, NM_001278428.3:c.1317C>T, NM_001278428.2:c.1317C>A, NM_001278428.2:c.1317C>T, NM_001278426.4:c.1317C>A, NM_001278426.4:c.1317C>T, NM_001278426.3:c.1317C>A, NM_001278426.3:c.1317C>T, NM_001278426.2:c.1317C>A, NM_001278426.2:c.1317C>T, NM_001278427.4:c.1314C>A, NM_001278427.4:c.1314C>T, NM_001278427.3:c.1314C>A, NM_001278427.3:c.1314C>T, NM_001278427.2:c.1314C>A, NM_001278427.2:c.1314C>T, NM_001278429.4:c.1284C>A, NM_001278429.4:c.1284C>T, NM_001278429.3:c.1407C>A, NM_001278429.3:c.1407C>T, NM_001278429.2:c.1407C>A, NM_001278429.2:c.1407C>T, NM_006847.3:c.1317C>A, NM_006847.3:c.1317C>T, NM_006847.1:c.1317C>A, NM_006847.1:c.1317C>T, NM_001394937.1:c.1278C>A, NM_001394937.1:c.1278C>T, NM_001081438.1:c.1314C>A, NM_001081438.1:c.1314C>T, NM_006847.2:c.1317C>A, NM_006847.2:c.1317C>T, XM_017026216.2:c.1317C>A, XM_017026216.2:c.1317C>T, XM_017026216.1:c.1440C>A, XM_017026216.1:c.1440C>T, NM_001394933.1:c.1320C>A, NM_001394933.1:c.1320C>T, NM_001394934.1:c.1314C>A, NM_001394934.1:c.1314C>T, XM_047438103.1:c.1059C>A, XM_047438103.1:c.1059C>T, NM_001394938.1:c.1170C>A, NM_001394938.1:c.1170C>T, NM_001394935.1:c.1311C>A, NM_001394935.1:c.1311C>T, NM_001394936.1:c.1281C>A, NM_001394936.1:c.1281C>T, XM_047438101.1:c.1275C>A, XM_047438101.1:c.1275C>T, NM_001394939.1:c.1158C>A, NM_001394939.1:c.1158C>T, XM_047438100.1:c.1278C>A, XM_047438100.1:c.1278C>T

          5.

          rs1484371008 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>T [Show Flanks]
            Chromosome:
            19:54665885 (GRCh38)
            19:55177336 (GRCh37)
            Canonical SPDI:
            NC_000019.10:54665884:C:T
            Gene:
            LILRB4 (Varview)
            Functional Consequence:
            synonymous_variant,genic_downstream_transcript_variant,coding_sequence_variant
            Validated:
            by frequency
            MAF:
            T=0.000004/1 (GnomAD_exomes)
            HGVS:
            NC_000019.10:g.54665885C>T, NW_004166865.1:g.640252C>T, NW_003571061.2:g.392389C>T, NW_003571061.1:g.392388C>T, NT_187693.1:g.648450C>T, NC_000019.9:g.55177336C>T, NW_003571060.1:g.570767C>T, NW_003571054.1:g.572288C>T, NM_001278428.4:c.828C>T, NM_001278428.3:c.828C>T, NM_001278428.2:c.828C>T, NM_001278426.4:c.828C>T, NM_001278426.3:c.828C>T, NM_001278426.2:c.828C>T, NM_001278427.4:c.828C>T, NM_001278427.3:c.828C>T, NM_001278427.2:c.828C>T, NM_001278429.4:c.792C>T, NM_001278429.3:c.915C>T, NM_001278429.2:c.915C>T, NM_006847.3:c.828C>T, NM_006847.2:c.828C>T, XM_017026216.2:c.825C>T, XM_017026216.1:c.948C>T, NM_001394934.1:c.825C>T, NM_001394936.1:c.792C>T, XM_047438102.1:c.828C>T, NM_006847.1:c.828C>T, NM_001394935.1:c.825C>T, XM_047438100.1:c.792C>T, XM_047438101.1:c.789C>T, XM_047438103.1:c.567C>T, NM_001394938.1:c.792C>T, NM_001394939.1:c.828C>T, NM_001081438.1:c.828C>T, NM_001394933.1:c.828C>T, NM_001394937.1:c.789C>T

            6.

            rs1483463835 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>C [Show Flanks]
              Chromosome:
              19:54667906 (GRCh38)
              19:55179357 (GRCh37)
              Canonical SPDI:
              NC_000019.10:54667905:T:C
              Gene:
              LILRB4 (Varview)
              Functional Consequence:
              genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
              Validated:
              by frequency,by alfa
              MAF:
              C=0.000071/1 (ALFA)
              C=0.000004/1 (TOPMED)
              HGVS:
              NC_000019.10:g.54667906T>C, NW_004166865.1:g.642273T>C, NW_003571061.2:g.394410T>C, NW_003571061.1:g.394409T>C, NT_187693.1:g.650471T>C, NC_000019.9:g.55179357T>C, NW_003571060.1:g.572788T>C, NW_003571054.1:g.574309T>C, NM_001278428.4:c.1234T>C, NM_001278428.3:c.1234T>C, NM_001278428.2:c.1234T>C, NM_001278426.4:c.1234T>C, NM_001278426.3:c.1234T>C, NM_001278426.2:c.1234T>C, NM_001278427.4:c.1231T>C, NM_001278427.3:c.1231T>C, NM_001278427.2:c.1231T>C, NM_001278429.4:c.1201T>C, NM_001278429.3:c.1324T>C, NM_001278429.2:c.1324T>C, NM_006847.3:c.1234T>C, NM_006847.1:c.1234T>C, NM_001394937.1:c.1195T>C, NM_001081438.1:c.1231T>C, NM_006847.2:c.1234T>C, XM_017026216.2:c.1234T>C, XM_017026216.1:c.1357T>C, NM_001394934.1:c.1231T>C, XM_047438101.1:c.1192T>C, XM_047438103.1:c.976T>C, NM_001394933.1:c.1237T>C, NM_001394938.1:c.1087T>C, NM_001394935.1:c.1228T>C, NM_001394936.1:c.1198T>C, NM_001394939.1:c.1075T>C, XM_047438100.1:c.1195T>C, NP_001265357.2:p.Tyr412His, NP_001265355.2:p.Tyr412His, NP_001265356.2:p.Tyr411His, NP_001265358.3:p.Tyr401His, NP_001381866.1:p.Tyr399His, XP_016881705.2:p.Tyr412His, NP_001381863.1:p.Tyr411His, XP_047294057.1:p.Tyr398His, XP_047294059.1:p.Tyr326His, NP_001381862.1:p.Tyr413His, NP_001381867.1:p.Tyr363His, NP_001381864.1:p.Tyr410His, NP_001381865.1:p.Tyr400His, NP_001381868.1:p.Tyr359His, XP_047294056.1:p.Tyr399His

              7.

              rs1479827818 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>A,T [Show Flanks]
                Chromosome:
                19:54667932 (GRCh38)
                19:55179383 (GRCh37)
                Canonical SPDI:
                NC_000019.10:54667931:C:A,NC_000019.10:54667931:C:T
                Gene:
                LILRB4 (Varview)
                Functional Consequence:
                synonymous_variant,genic_downstream_transcript_variant,coding_sequence_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                T=0.00006/2 (ALFA)
                T=0.000008/2 (GnomAD_exomes)
                T=0.000014/2 (GnomAD)
                HGVS:
                NC_000019.10:g.54667932C>A, NC_000019.10:g.54667932C>T, NW_004166865.1:g.642299C>A, NW_004166865.1:g.642299C>T, NW_003571061.2:g.394436C>A, NW_003571061.2:g.394436C>T, NW_003571061.1:g.394435C>A, NW_003571061.1:g.394435C>T, NT_187693.1:g.650497C>A, NT_187693.1:g.650497C>T, NC_000019.9:g.55179383C>A, NC_000019.9:g.55179383C>T, NW_003571060.1:g.572814C>A, NW_003571060.1:g.572814C>T, NW_003571054.1:g.574335C>A, NW_003571054.1:g.574335C>T, NM_001278428.4:c.1260C>A, NM_001278428.4:c.1260C>T, NM_001278428.3:c.1260C>A, NM_001278428.3:c.1260C>T, NM_001278428.2:c.1260C>A, NM_001278428.2:c.1260C>T, NM_001278426.4:c.1260C>A, NM_001278426.4:c.1260C>T, NM_001278426.3:c.1260C>A, NM_001278426.3:c.1260C>T, NM_001278426.2:c.1260C>A, NM_001278426.2:c.1260C>T, NM_001278427.4:c.1257C>A, NM_001278427.4:c.1257C>T, NM_001278427.3:c.1257C>A, NM_001278427.3:c.1257C>T, NM_001278427.2:c.1257C>A, NM_001278427.2:c.1257C>T, NM_001278429.4:c.1227C>A, NM_001278429.4:c.1227C>T, NM_001278429.3:c.1350C>A, NM_001278429.3:c.1350C>T, NM_001278429.2:c.1350C>A, NM_001278429.2:c.1350C>T, NM_006847.3:c.1260C>A, NM_006847.3:c.1260C>T, NM_006847.1:c.1260C>A, NM_006847.1:c.1260C>T, NM_006847.2:c.1260C>A, NM_006847.2:c.1260C>T, XM_017026216.2:c.1260C>A, XM_017026216.2:c.1260C>T, XM_017026216.1:c.1383C>A, XM_017026216.1:c.1383C>T, NM_001394933.1:c.1263C>A, NM_001394933.1:c.1263C>T, NM_001394934.1:c.1257C>A, NM_001394934.1:c.1257C>T, NM_001394935.1:c.1254C>A, NM_001394935.1:c.1254C>T, XM_047438101.1:c.1218C>A, XM_047438101.1:c.1218C>T, NM_001394938.1:c.1113C>A, NM_001394938.1:c.1113C>T, NM_001081438.1:c.1257C>A, NM_001081438.1:c.1257C>T, XM_047438103.1:c.1002C>A, XM_047438103.1:c.1002C>T, NM_001394937.1:c.1221C>A, NM_001394937.1:c.1221C>T, NM_001394936.1:c.1224C>A, NM_001394936.1:c.1224C>T, XM_047438100.1:c.1221C>A, XM_047438100.1:c.1221C>T, NM_001394939.1:c.1101C>A, NM_001394939.1:c.1101C>T

                8.

                rs1479138051 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  T>G [Show Flanks]
                  Chromosome:
                  19:54667744 (GRCh38)
                  19:55179195 (GRCh37)
                  Canonical SPDI:
                  NC_000019.10:54667743:T:G
                  Gene:
                  LILRB4 (Varview)
                  Functional Consequence:
                  genic_downstream_transcript_variant,missense_variant,intron_variant,coding_sequence_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0./0 (ALFA)
                  G=0.000004/1 (TOPMED)
                  G=0.000007/1 (GnomAD)
                  HGVS:
                  NC_000019.10:g.54667744T>G, NW_004166865.1:g.642111T>G, NW_003571061.2:g.394248T>G, NW_003571061.1:g.394247T>G, NT_187693.1:g.650309T>G, NC_000019.9:g.55179195T>G, NW_003571060.1:g.572626T>G, NW_003571054.1:g.574147T>G, NM_001278428.4:c.1151T>G, NM_001278428.3:c.1151T>G, NM_001278428.2:c.1151T>G, NM_001278426.4:c.1151T>G, NM_001278426.3:c.1151T>G, NM_001278426.2:c.1151T>G, NM_001278427.4:c.1148T>G, NM_001278427.3:c.1148T>G, NM_001278427.2:c.1148T>G, NM_001278429.4:c.1118T>G, NM_001278429.3:c.1241T>G, NM_001278429.2:c.1241T>G, NM_006847.3:c.1151T>G, XM_017026216.2:c.1151T>G, XM_017026216.1:c.1274T>G, NM_006847.2:c.1151T>G, XM_047438100.1:c.1112T>G, NM_006847.1:c.1151T>G, NM_001394934.1:c.1148T>G, NM_001394935.1:c.1145T>G, NM_001394937.1:c.1112T>G, XM_047438101.1:c.1109T>G, XM_047438103.1:c.893T>G, NM_001081438.1:c.1148T>G, NM_001394933.1:c.1154T>G, NM_001394936.1:c.1115T>G, NM_001394938.1:c.1004T>G, NP_001265357.2:p.Leu384Arg, NP_001265355.2:p.Leu384Arg, NP_001265356.2:p.Leu383Arg, NP_001265358.3:p.Leu373Arg, XP_016881705.2:p.Leu384Arg, XP_047294056.1:p.Leu371Arg, NP_001381863.1:p.Leu383Arg, NP_001381864.1:p.Leu382Arg, NP_001381866.1:p.Leu371Arg, XP_047294057.1:p.Leu370Arg, XP_047294059.1:p.Leu298Arg, NP_001381862.1:p.Leu385Arg, NP_001381865.1:p.Leu372Arg, NP_001381867.1:p.Leu335Arg

                  9.

                  rs1476472075 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    T>C [Show Flanks]
                    Chromosome:
                    19:54667718 (GRCh38)
                    19:55179169 (GRCh37)
                    Canonical SPDI:
                    NC_000019.10:54667717:T:C
                    Gene:
                    LILRB4 (Varview)
                    Functional Consequence:
                    synonymous_variant,genic_downstream_transcript_variant,intron_variant,coding_sequence_variant
                    Validated:
                    by frequency
                    MAF:
                    C=0.000008/2 (GnomAD_exomes)
                    HGVS:
                    NC_000019.10:g.54667718T>C, NW_004166865.1:g.642085T>C, NW_003571061.2:g.394222T>C, NW_003571061.1:g.394221T>C, NT_187693.1:g.650283T>C, NC_000019.9:g.55179169T>C, NW_003571060.1:g.572600T>C, NW_003571054.1:g.574121T>C, NM_001278428.4:c.1125T>C, NM_001278428.3:c.1125T>C, NM_001278428.2:c.1125T>C, NM_001278426.4:c.1125T>C, NM_001278426.3:c.1125T>C, NM_001278426.2:c.1125T>C, NM_001278427.4:c.1122T>C, NM_001278427.3:c.1122T>C, NM_001278427.2:c.1122T>C, NM_001278429.4:c.1092T>C, NM_001278429.3:c.1215T>C, NM_001278429.2:c.1215T>C, NM_006847.3:c.1125T>C, NM_006847.1:c.1125T>C, NM_006847.2:c.1125T>C, XM_017026216.2:c.1125T>C, XM_017026216.1:c.1248T>C, NM_001394933.1:c.1128T>C, NM_001394934.1:c.1122T>C, NM_001394935.1:c.1119T>C, XM_047438101.1:c.1083T>C, NM_001394938.1:c.978T>C, NM_001081438.1:c.1122T>C, XM_047438103.1:c.867T>C, NM_001394937.1:c.1086T>C, NM_001394936.1:c.1089T>C, XM_047438100.1:c.1086T>C

                    10.

                    rs1472174635 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>A,G [Show Flanks]
                      Chromosome:
                      19:54667655 (GRCh38)
                      19:55179106 (GRCh37)
                      Canonical SPDI:
                      NC_000019.10:54667654:C:A,NC_000019.10:54667654:C:G
                      Gene:
                      LILRB4 (Varview)
                      Functional Consequence:
                      genic_downstream_transcript_variant,missense_variant,intron_variant,coding_sequence_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0./0 (ALFA)
                      A=0.000004/1 (GnomAD_exomes)
                      A=0.000004/1 (TOPMED)
                      G=0.000035/1 (TOMMO)
                      HGVS:
                      NC_000019.10:g.54667655C>A, NC_000019.10:g.54667655C>G, NW_004166865.1:g.642022C>A, NW_004166865.1:g.642022C>G, NW_003571061.2:g.394159C>A, NW_003571061.2:g.394159C>G, NW_003571061.1:g.394158C>A, NW_003571061.1:g.394158C>G, NT_187693.1:g.650220C>A, NT_187693.1:g.650220C>G, NC_000019.9:g.55179106C>A, NC_000019.9:g.55179106C>G, NW_003571060.1:g.572537C>A, NW_003571060.1:g.572537C>G, NW_003571054.1:g.574058C>A, NW_003571054.1:g.574058C>G, NM_001278428.4:c.1062C>A, NM_001278428.4:c.1062C>G, NM_001278428.3:c.1062C>A, NM_001278428.3:c.1062C>G, NM_001278428.2:c.1062C>A, NM_001278428.2:c.1062C>G, NM_001278426.4:c.1062C>A, NM_001278426.4:c.1062C>G, NM_001278426.3:c.1062C>A, NM_001278426.3:c.1062C>G, NM_001278426.2:c.1062C>A, NM_001278426.2:c.1062C>G, NM_001278427.4:c.1059C>A, NM_001278427.4:c.1059C>G, NM_001278427.3:c.1059C>A, NM_001278427.3:c.1059C>G, NM_001278427.2:c.1059C>A, NM_001278427.2:c.1059C>G, NM_001278429.4:c.1029C>A, NM_001278429.4:c.1029C>G, NM_001278429.3:c.1152C>A, NM_001278429.3:c.1152C>G, NM_001278429.2:c.1152C>A, NM_001278429.2:c.1152C>G, NM_006847.3:c.1062C>A, NM_006847.3:c.1062C>G, NM_006847.1:c.1062C>A, NM_006847.1:c.1062C>G, NM_001394936.1:c.1026C>A, NM_001394936.1:c.1026C>G, XM_017026216.2:c.1062C>A, XM_017026216.2:c.1062C>G, XM_017026216.1:c.1185C>A, XM_017026216.1:c.1185C>G, NM_006847.2:c.1062C>A, NM_006847.2:c.1062C>G, XM_047438100.1:c.1023C>A, XM_047438100.1:c.1023C>G, XM_047438103.1:c.804C>A, XM_047438103.1:c.804C>G, NM_001394938.1:c.915C>A, NM_001394938.1:c.915C>G, NM_001081438.1:c.1059C>A, NM_001081438.1:c.1059C>G, NM_001394934.1:c.1059C>A, NM_001394934.1:c.1059C>G, NM_001394933.1:c.1065C>A, NM_001394933.1:c.1065C>G, NM_001394935.1:c.1056C>A, NM_001394935.1:c.1056C>G, NM_001394937.1:c.1023C>A, NM_001394937.1:c.1023C>G, XM_047438101.1:c.1020C>A, XM_047438101.1:c.1020C>G, NP_001265357.2:p.Asp354Glu, NP_001265357.2:p.Asp354Glu, NP_001265355.2:p.Asp354Glu, NP_001265355.2:p.Asp354Glu, NP_001265356.2:p.Asp353Glu, NP_001265356.2:p.Asp353Glu, NP_001265358.3:p.Asp343Glu, NP_001265358.3:p.Asp343Glu, NP_001381865.1:p.Asp342Glu, NP_001381865.1:p.Asp342Glu, XP_016881705.2:p.Asp354Glu, XP_016881705.2:p.Asp354Glu, XP_047294056.1:p.Asp341Glu, XP_047294056.1:p.Asp341Glu, XP_047294059.1:p.Asp268Glu, XP_047294059.1:p.Asp268Glu, NP_001381867.1:p.Asp305Glu, NP_001381867.1:p.Asp305Glu, NP_001381863.1:p.Asp353Glu, NP_001381863.1:p.Asp353Glu, NP_001381862.1:p.Asp355Glu, NP_001381862.1:p.Asp355Glu, NP_001381864.1:p.Asp352Glu, NP_001381864.1:p.Asp352Glu, NP_001381866.1:p.Asp341Glu, NP_001381866.1:p.Asp341Glu, XP_047294057.1:p.Asp340Glu, XP_047294057.1:p.Asp340Glu

                      11.

                      rs1471498408 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        19:54663762 (GRCh38)
                        19:55175220 (GRCh37)
                        Canonical SPDI:
                        NC_000019.10:54663761:C:T
                        Gene:
                        LILRB4 (Varview)
                        Functional Consequence:
                        missense_variant,intron_variant,coding_sequence_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000004/1 (GnomAD_exomes)
                        T=0.000008/2 (TOPMED)
                        HGVS:
                        NC_000019.10:g.54663762C>T, NW_004166865.1:g.638129C>T, NW_003571061.2:g.390266C>T, NW_003571061.1:g.390265C>T, NT_187693.1:g.646334C>T, NC_000019.9:g.55175220C>T, NW_003571060.1:g.568644C>T, NW_003571054.1:g.570165C>T, NM_001278428.4:c.79C>T, NM_001278428.3:c.79C>T, NM_001278428.2:c.79C>T, NM_001278426.4:c.79C>T, NM_001278426.3:c.79C>T, NM_001278426.2:c.79C>T, NM_001278427.4:c.79C>T, NM_001278427.3:c.79C>T, NM_001278427.2:c.79C>T, NM_001278429.4:c.43C>T, NM_001278429.3:c.166C>T, NM_001278429.2:c.166C>T, NM_001278430.4:c.79C>T, NM_001278430.3:c.79C>T, NM_001278430.2:c.79C>T, NM_006847.3:c.79C>T, XM_017026216.2:c.79C>T, XM_017026216.1:c.202C>T, NM_001394939.1:c.79C>T, NM_001394937.1:c.43C>T, NM_006847.2:c.79C>T, NM_001394933.1:c.79C>T, NM_001394934.1:c.79C>T, XM_047438102.1:c.79C>T, NM_001081438.1:c.79C>T, NM_006847.1:c.79C>T, NM_001394936.1:c.43C>T, NM_001394938.1:c.43C>T, NM_001394935.1:c.79C>T, XM_047438100.1:c.43C>T, XM_047438101.1:c.43C>T, NP_001265357.2:p.Pro27Ser, NP_001265355.2:p.Pro27Ser, NP_001265356.2:p.Pro27Ser, NP_001265358.3:p.Pro15Ser, NP_001265359.2:p.Pro27Ser, XP_016881705.2:p.Pro27Ser, NP_001381868.1:p.Pro27Ser, NP_001381866.1:p.Pro15Ser, NP_001381862.1:p.Pro27Ser, NP_001381863.1:p.Pro27Ser, XP_047294058.1:p.Pro27Ser, NP_001381865.1:p.Pro15Ser, NP_001381867.1:p.Pro15Ser, NP_001381864.1:p.Pro27Ser, XP_047294056.1:p.Pro15Ser, XP_047294057.1:p.Pro15Ser

                        12.

                        rs1470013219 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>A [Show Flanks]
                          Chromosome:
                          19:54664206 (GRCh38)
                          19:55175657 (GRCh37)
                          Canonical SPDI:
                          NC_000019.10:54664205:C:A
                          Gene:
                          LILRB4 (Varview)
                          Functional Consequence:
                          missense_variant,coding_sequence_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_000019.10:g.54664206C>A, NW_004166865.1:g.638573C>A, NW_003571061.2:g.390710C>A, NW_003571061.1:g.390709C>A, NT_187693.1:g.646771C>A, NC_000019.9:g.55175657C>A, NW_003571060.1:g.569088C>A, NW_003571054.1:g.570609C>A, NM_001278428.4:c.376C>A, NM_001278428.3:c.376C>A, NM_001278428.2:c.376C>A, NM_001278426.4:c.376C>A, NM_001278426.3:c.376C>A, NM_001278426.2:c.376C>A, NM_001278427.4:c.376C>A, NM_001278427.3:c.376C>A, NM_001278427.2:c.376C>A, NM_001278429.4:c.340C>A, NM_001278429.3:c.463C>A, NM_001278429.2:c.463C>A, NM_001278430.4:c.376C>A, NM_001278430.3:c.376C>A, NM_001278430.2:c.376C>A, NM_006847.3:c.376C>A, XM_017026216.2:c.376C>A, XM_017026216.1:c.499C>A, NM_006847.2:c.376C>A, NM_001394933.1:c.376C>A, NM_001394934.1:c.376C>A, XM_047438100.1:c.340C>A, NM_001394937.1:c.340C>A, XM_047438101.1:c.340C>A, NM_001394938.1:c.340C>A, NM_001394935.1:c.376C>A, NM_001394936.1:c.340C>A, NM_001394939.1:c.376C>A, NM_001081438.1:c.376C>A, NM_006847.1:c.376C>A, XM_047438102.1:c.376C>A, XM_047438103.1:c.115C>A, NP_001265357.2:p.Leu126Ile, NP_001265355.2:p.Leu126Ile, NP_001265356.2:p.Leu126Ile, NP_001265358.3:p.Leu114Ile, NP_001265359.2:p.Leu126Ile, XP_016881705.2:p.Leu126Ile, NP_001381862.1:p.Leu126Ile, NP_001381863.1:p.Leu126Ile, XP_047294056.1:p.Leu114Ile, NP_001381866.1:p.Leu114Ile, XP_047294057.1:p.Leu114Ile, NP_001381867.1:p.Leu114Ile, NP_001381864.1:p.Leu126Ile, NP_001381865.1:p.Leu114Ile, NP_001381868.1:p.Leu126Ile, XP_047294058.1:p.Leu126Ile, XP_047294059.1:p.Leu39Ile

                          13.

                          rs1468090082 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A [Show Flanks]
                            Chromosome:
                            19:54664485 (GRCh38)
                            19:55175936 (GRCh37)
                            Canonical SPDI:
                            NC_000019.10:54664484:G:A
                            Gene:
                            LILRB4 (Varview)
                            Functional Consequence:
                            missense_variant,coding_sequence_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_000019.10:g.54664485G>A, NW_004166865.1:g.638852G>A, NW_003571061.2:g.390989G>A, NW_003571061.1:g.390988G>A, NT_187693.1:g.647050G>A, NC_000019.9:g.55175936G>A, NW_003571060.1:g.569367G>A, NW_003571054.1:g.570888G>A, NM_001278428.4:c.655G>A, NM_001278428.3:c.655G>A, NM_001278428.2:c.655G>A, NM_001278426.4:c.655G>A, NM_001278426.3:c.655G>A, NM_001278426.2:c.655G>A, NM_001278427.4:c.655G>A, NM_001278427.3:c.655G>A, NM_001278427.2:c.655G>A, NM_001278429.4:c.619G>A, NM_001278429.3:c.742G>A, NM_001278429.2:c.742G>A, NM_001278430.4:c.655G>A, NM_001278430.3:c.655G>A, NM_001278430.2:c.655G>A, NM_006847.3:c.655G>A, XM_017026216.2:c.655G>A, XM_017026216.1:c.778G>A, NM_001394934.1:c.655G>A, NM_006847.2:c.655G>A, NM_001394933.1:c.655G>A, XM_047438100.1:c.619G>A, XM_047438101.1:c.619G>A, XM_047438103.1:c.394G>A, NM_001394938.1:c.619G>A, NM_006847.1:c.655G>A, NM_001394935.1:c.655G>A, NM_001394936.1:c.619G>A, NM_001081438.1:c.655G>A, NM_001394937.1:c.619G>A, NM_001394939.1:c.655G>A, XM_047438102.1:c.655G>A, NP_001265357.2:p.Gly219Arg, NP_001265355.2:p.Gly219Arg, NP_001265356.2:p.Gly219Arg, NP_001265358.3:p.Gly207Arg, NP_001265359.2:p.Gly219Arg, XP_016881705.2:p.Gly219Arg, NP_001381863.1:p.Gly219Arg, NP_001381862.1:p.Gly219Arg, XP_047294056.1:p.Gly207Arg, XP_047294057.1:p.Gly207Arg, XP_047294059.1:p.Gly132Arg, NP_001381867.1:p.Gly207Arg, NP_001381864.1:p.Gly219Arg, NP_001381865.1:p.Gly207Arg, NP_001381866.1:p.Gly207Arg, NP_001381868.1:p.Gly219Arg, XP_047294058.1:p.Gly219Arg

                            14.

                            rs1467173859 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A [Show Flanks]
                              Chromosome:
                              19:54664222 (GRCh38)
                              19:55175673 (GRCh37)
                              Canonical SPDI:
                              NC_000019.10:54664221:G:A
                              Gene:
                              LILRB4 (Varview)
                              Functional Consequence:
                              missense_variant,coding_sequence_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              A=0./0 (ALFA)
                              A=0.000007/1 (GnomAD)
                              A=0.000011/3 (TOPMED)
                              HGVS:
                              NC_000019.10:g.54664222G>A, NW_004166865.1:g.638589G>A, NW_003571061.2:g.390726G>A, NW_003571061.1:g.390725G>A, NT_187693.1:g.646787G>A, NC_000019.9:g.55175673G>A, NW_003571060.1:g.569104G>A, NW_003571054.1:g.570625G>A, NM_001278428.4:c.392G>A, NM_001278428.3:c.392G>A, NM_001278428.2:c.392G>A, NM_001278426.4:c.392G>A, NM_001278426.3:c.392G>A, NM_001278426.2:c.392G>A, NM_001278427.4:c.392G>A, NM_001278427.3:c.392G>A, NM_001278427.2:c.392G>A, NM_001278429.4:c.356G>A, NM_001278429.3:c.479G>A, NM_001278429.2:c.479G>A, NM_001278430.4:c.392G>A, NM_001278430.3:c.392G>A, NM_001278430.2:c.392G>A, NM_006847.3:c.392G>A, XM_017026216.2:c.392G>A, XM_017026216.1:c.515G>A, NM_001394934.1:c.392G>A, NM_006847.2:c.392G>A, NM_001394933.1:c.392G>A, XM_047438100.1:c.356G>A, XM_047438101.1:c.356G>A, XM_047438103.1:c.131G>A, NM_001394938.1:c.356G>A, NM_006847.1:c.392G>A, NM_001394935.1:c.392G>A, NM_001394936.1:c.356G>A, NM_001081438.1:c.392G>A, NM_001394937.1:c.356G>A, NM_001394939.1:c.392G>A, XM_047438102.1:c.392G>A, NP_001265357.2:p.Ser131Asn, NP_001265355.2:p.Ser131Asn, NP_001265356.2:p.Ser131Asn, NP_001265358.3:p.Ser119Asn, NP_001265359.2:p.Ser131Asn, XP_016881705.2:p.Ser131Asn, NP_001381863.1:p.Ser131Asn, NP_001381862.1:p.Ser131Asn, XP_047294056.1:p.Ser119Asn, XP_047294057.1:p.Ser119Asn, XP_047294059.1:p.Ser44Asn, NP_001381867.1:p.Ser119Asn, NP_001381864.1:p.Ser131Asn, NP_001381865.1:p.Ser119Asn, NP_001381866.1:p.Ser119Asn, NP_001381868.1:p.Ser131Asn, XP_047294058.1:p.Ser131Asn

                              15.

                              rs1465580006 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                19:54664815 (GRCh38)
                                19:55176266 (GRCh37)
                                Canonical SPDI:
                                NC_000019.10:54664814:C:T
                                Gene:
                                LILRB4 (Varview)
                                Functional Consequence:
                                coding_sequence_variant,synonymous_variant
                                HGVS:
                                NC_000019.10:g.54664815C>T, NW_004166865.1:g.639182C>T, NW_003571061.2:g.391319C>T, NW_003571061.1:g.391318C>T, NT_187693.1:g.647380C>T, NC_000019.9:g.55176266C>T, NW_003571060.1:g.569697C>T, NW_003571054.1:g.571218C>T, NM_001278428.4:c.672C>T, NM_001278428.3:c.672C>T, NM_001278428.2:c.672C>T, NM_001278426.4:c.672C>T, NM_001278426.3:c.672C>T, NM_001278426.2:c.672C>T, NM_001278427.4:c.672C>T, NM_001278427.3:c.672C>T, NM_001278427.2:c.672C>T, NM_001278429.4:c.636C>T, NM_001278429.3:c.759C>T, NM_001278429.2:c.759C>T, NM_001278430.4:c.672C>T, NM_001278430.3:c.672C>T, NM_001278430.2:c.672C>T, NM_006847.3:c.672C>T, XM_017026216.2:c.672C>T, XM_017026216.1:c.795C>T, NM_001394939.1:c.672C>T, NM_006847.2:c.672C>T, NM_001394933.1:c.672C>T, NM_001394934.1:c.672C>T, XM_047438100.1:c.636C>T, NM_001394937.1:c.636C>T, XM_047438101.1:c.636C>T, XM_047438103.1:c.411C>T, NM_001394938.1:c.636C>T, NM_001081438.1:c.672C>T, NM_001394935.1:c.672C>T, NM_001394936.1:c.636C>T, XM_047438102.1:c.672C>T, NM_006847.1:c.672C>T

                                16.

                                rs1463212750 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>C [Show Flanks]
                                  Chromosome:
                                  19:54663536 (GRCh38)
                                  19:55174994 (GRCh37)
                                  Canonical SPDI:
                                  NC_000019.10:54663535:G:C
                                  Gene:
                                  LILRB4 (Varview)
                                  Functional Consequence:
                                  intron_variant,coding_sequence_variant,synonymous_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  C=0.000111/1 (ALFA)
                                  C=0.000004/1 (GnomAD_exomes)
                                  HGVS:

                                  17.

                                  rs1458248194 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>G [Show Flanks]
                                    Chromosome:
                                    19:54668011 (GRCh38)
                                    19:55179462 (GRCh37)
                                    Canonical SPDI:
                                    NC_000019.10:54668010:A:G
                                    Gene:
                                    LILRB4 (Varview)
                                    Functional Consequence:
                                    genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    G=0./0 (ALFA)
                                    G=0.000008/2 (TOPMED)
                                    HGVS:
                                    NC_000019.10:g.54668011A>G, NW_004166865.1:g.642378A>G, NW_003571061.2:g.394515A>G, NW_003571061.1:g.394514A>G, NT_187693.1:g.650576A>G, NC_000019.9:g.55179462A>G, NW_003571060.1:g.572893A>G, NW_003571054.1:g.574414A>G, NM_001278428.4:c.1339A>G, NM_001278428.3:c.1339A>G, NM_001278428.2:c.1339A>G, NM_001278426.4:c.1339A>G, NM_001278426.3:c.1339A>G, NM_001278426.2:c.1339A>G, NM_001278427.4:c.1336A>G, NM_001278427.3:c.1336A>G, NM_001278427.2:c.1336A>G, NM_001278429.4:c.1306A>G, NM_001278429.3:c.1429A>G, NM_001278429.2:c.1429A>G, NM_006847.3:c.1339A>G, XM_017026216.2:c.1339A>G, XM_017026216.1:c.1462A>G, NM_006847.1:c.1339A>G, NM_001394937.1:c.1300A>G, NM_001394936.1:c.1303A>G, NM_001394938.1:c.1192A>G, NM_006847.2:c.1339A>G, NM_001394933.1:c.1342A>G, NM_001394934.1:c.1336A>G, XM_047438101.1:c.1297A>G, XM_047438103.1:c.1081A>G, NM_001081438.1:c.1336A>G, NM_001394939.1:c.1180A>G, XM_047438100.1:c.1300A>G, NM_001394935.1:c.1333A>G, NP_001265357.2:p.Ile447Val, NP_001265355.2:p.Ile447Val, NP_001265356.2:p.Ile446Val, NP_001265358.3:p.Ile436Val, XP_016881705.2:p.Ile447Val, NP_001381866.1:p.Ile434Val, NP_001381865.1:p.Ile435Val, NP_001381867.1:p.Ile398Val, NP_001381862.1:p.Ile448Val, NP_001381863.1:p.Ile446Val, XP_047294057.1:p.Ile433Val, XP_047294059.1:p.Ile361Val, NP_001381868.1:p.Ile394Val, XP_047294056.1:p.Ile434Val, NP_001381864.1:p.Ile445Val

                                    18.

                                    rs1455677947 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>A [Show Flanks]
                                      Chromosome:
                                      19:54663845 (GRCh38)
                                      19:55175303 (GRCh37)
                                      Canonical SPDI:
                                      NC_000019.10:54663844:G:A
                                      Gene:
                                      LILRB4 (Varview)
                                      Functional Consequence:
                                      5_prime_UTR_variant,coding_sequence_variant,synonymous_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      A=0.000071/1 (ALFA)
                                      A=0.000004/1 (TOPMED)
                                      A=0.000007/1 (GnomAD)
                                      HGVS:
                                      NC_000019.10:g.54663845G>A, NW_004166865.1:g.638212G>A, NW_003571061.2:g.390349G>A, NW_003571061.1:g.390348G>A, NT_187693.1:g.646417G>A, NC_000019.9:g.55175303G>A, NW_003571060.1:g.568727G>A, NW_003571054.1:g.570248G>A, NM_001278428.4:c.162G>A, NM_001278428.3:c.162G>A, NM_001278428.2:c.162G>A, NM_001278426.4:c.162G>A, NM_001278426.3:c.162G>A, NM_001278426.2:c.162G>A, NM_001278427.4:c.162G>A, NM_001278427.3:c.162G>A, NM_001278427.2:c.162G>A, NM_001278429.4:c.126G>A, NM_001278429.3:c.249G>A, NM_001278429.2:c.249G>A, NM_001278430.4:c.162G>A, NM_001278430.3:c.162G>A, NM_001278430.2:c.162G>A, NM_006847.3:c.162G>A, NM_006847.2:c.162G>A, XM_017026216.2:c.162G>A, XM_017026216.1:c.285G>A, NM_001394933.1:c.162G>A, NM_001394934.1:c.162G>A, NM_001394935.1:c.162G>A, XM_047438100.1:c.126G>A, XM_047438103.1:c.-100G>A, NM_001394939.1:c.162G>A, NM_001081438.1:c.162G>A, NM_001394936.1:c.126G>A, NM_001394937.1:c.126G>A, NM_001394938.1:c.126G>A, XM_047438101.1:c.126G>A, NM_006847.1:c.162G>A, XM_047438102.1:c.162G>A

                                      19.

                                      rs1453153837 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        19:54663541 (GRCh38)
                                        19:55174999 (GRCh37)
                                        Canonical SPDI:
                                        NC_000019.10:54663540:T:C
                                        Gene:
                                        LILRB4 (Varview)
                                        Functional Consequence:
                                        intron_variant,coding_sequence_variant,missense_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        C=0./0 (ALFA)
                                        C=0.000004/1 (GnomAD_exomes)
                                        C=0.000007/1 (GnomAD)
                                        HGVS:
                                        NC_000019.10:g.54663541T>C, NW_004166865.1:g.637908T>C, NW_003571061.2:g.390045T>C, NW_003571061.1:g.390044T>C, NT_187693.1:g.646113T>C, NC_000019.9:g.55174999T>C, NW_003571060.1:g.568423T>C, NW_003571054.1:g.569944T>C, NM_001278428.4:c.44T>C, NM_001278428.3:c.44T>C, NM_001278428.2:c.44T>C, NM_001278426.4:c.44T>C, NM_001278426.3:c.44T>C, NM_001278426.2:c.44T>C, NM_001278427.4:c.44T>C, NM_001278427.3:c.44T>C, NM_001278427.2:c.44T>C, NM_001278430.4:c.44T>C, NM_001278430.3:c.44T>C, NM_001278430.2:c.44T>C, NM_006847.3:c.44T>C, NM_006847.2:c.44T>C, XM_017026216.2:c.44T>C, XM_017026216.1:c.167T>C, NM_001394934.1:c.44T>C, NM_001394939.1:c.44T>C, NM_006847.1:c.44T>C, NM_001394933.1:c.44T>C, NM_001081438.1:c.44T>C, XM_047438102.1:c.44T>C, NM_001394935.1:c.44T>C, NP_001265357.2:p.Leu15Pro, NP_001265355.2:p.Leu15Pro, NP_001265356.2:p.Leu15Pro, NP_001265359.2:p.Leu15Pro, XP_016881705.2:p.Leu15Pro, NP_001381863.1:p.Leu15Pro, NP_001381868.1:p.Leu15Pro, NP_001381862.1:p.Leu15Pro, XP_047294058.1:p.Leu15Pro, NP_001381864.1:p.Leu15Pro

                                        20.

                                        rs1446558047 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>G [Show Flanks]
                                          Chromosome:
                                          19:54663897 (GRCh38)
                                          19:55175355 (GRCh37)
                                          Canonical SPDI:
                                          NC_000019.10:54663896:C:G
                                          Gene:
                                          LILRB4 (Varview)
                                          Functional Consequence:
                                          5_prime_UTR_variant,coding_sequence_variant,missense_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          G=0./0 (ALFA)
                                          G=0.000004/1 (GnomAD_exomes)
                                          G=0.000004/1 (TOPMED)
                                          HGVS:
                                          NC_000019.10:g.54663897C>G, NW_004166865.1:g.638264C>G, NW_003571061.2:g.390401C>G, NW_003571061.1:g.390400C>G, NT_187693.1:g.646469C>G, NC_000019.9:g.55175355C>G, NW_003571060.1:g.568779C>G, NW_003571054.1:g.570300C>G, NM_001278428.4:c.214C>G, NM_001278428.3:c.214C>G, NM_001278428.2:c.214C>G, NM_001278426.4:c.214C>G, NM_001278426.3:c.214C>G, NM_001278426.2:c.214C>G, NM_001278427.4:c.214C>G, NM_001278427.3:c.214C>G, NM_001278427.2:c.214C>G, NM_001278429.4:c.178C>G, NM_001278429.3:c.301C>G, NM_001278429.2:c.301C>G, NM_001278430.4:c.214C>G, NM_001278430.3:c.214C>G, NM_001278430.2:c.214C>G, NM_006847.3:c.214C>G, XM_017026216.2:c.214C>G, XM_017026216.1:c.337C>G, NM_001394939.1:c.214C>G, NM_001394937.1:c.178C>G, NM_006847.2:c.214C>G, NM_001394933.1:c.214C>G, NM_001394934.1:c.214C>G, XM_047438102.1:c.214C>G, NM_001081438.1:c.214C>G, NM_006847.1:c.214C>G, NM_001394936.1:c.178C>G, NM_001394938.1:c.178C>G, NM_001394935.1:c.214C>G, XM_047438100.1:c.178C>G, XM_047438101.1:c.178C>G, XM_047438103.1:c.-48C>G, NP_001265357.2:p.Gln72Glu, NP_001265355.2:p.Gln72Glu, NP_001265356.2:p.Gln72Glu, NP_001265358.3:p.Gln60Glu, NP_001265359.2:p.Gln72Glu, XP_016881705.2:p.Gln72Glu, NP_001381868.1:p.Gln72Glu, NP_001381866.1:p.Gln60Glu, NP_001381862.1:p.Gln72Glu, NP_001381863.1:p.Gln72Glu, XP_047294058.1:p.Gln72Glu, NP_001381865.1:p.Gln60Glu, NP_001381867.1:p.Gln60Glu, NP_001381864.1:p.Gln72Glu, XP_047294056.1:p.Gln60Glu, XP_047294057.1:p.Gln60Glu

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