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Items: 1 to 20 of 169

1.

rs1490048400 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>T [Show Flanks]
    Chromosome:
    19:49486131 (GRCh38)
    19:49989388 (GRCh37)
    Canonical SPDI:
    NC_000019.10:49486130:G:T
    Gene:
    FLT3LG (Varview), RPL13A (Varview)
    Functional Consequence:
    2KB_upstream_variant,genic_downstream_transcript_variant,coding_sequence_variant,stop_gained,upstream_transcript_variant,3_prime_UTR_variant
    HGVS:
    NC_000019.10:g.49486131G>T, NC_000019.9:g.49989388G>T, NM_001459.4:c.*138G>T, NM_001459.3:c.*138G>T, XM_011526676.4:c.667G>T, XM_011526676.3:c.667G>T, XM_011526676.2:c.667G>T, XM_011526676.1:c.667G>T, XM_011526675.3:c.667G>T, XM_011526675.2:c.667G>T, XM_011526675.1:c.667G>T, XM_011526677.3:c.*157G>T, XM_011526678.3:c.613G>T, XM_011526678.2:c.613G>T, XM_011526678.1:c.613G>T, XM_011526680.3:c.*66G>T, XM_011526680.1:c.*66G>T, NM_001204502.2:c.*189G>T, NM_001204502.1:c.*189G>T, NM_001278637.2:c.*138G>T, NM_001278637.1:c.*138G>T, NM_001278638.2:c.*138G>T, NM_001278638.1:c.*138G>T, NM_001204503.2:c.*189G>T, NM_001204503.1:c.*189G>T, XM_047438522.1:c.*104G>T, XM_047438519.1:c.*66G>T, XM_047438523.1:c.*104G>T, XM_047438521.1:c.*104G>T, XP_011524978.1:p.Glu223Ter, XP_011524977.1:p.Glu223Ter, XP_011524980.1:p.Glu205Ter

    2.

    rs1480248972 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A [Show Flanks]
      Chromosome:
      19:49480584 (GRCh38)
      19:49983841 (GRCh37)
      Canonical SPDI:
      NC_000019.10:49480583:G:A
      Gene:
      FLT3LG (Varview)
      Functional Consequence:
      synonymous_variant,missense_variant,intron_variant,coding_sequence_variant
      HGVS:
      NC_000019.10:g.49480584G>A, NC_000019.9:g.49983841G>A, NM_001459.4:c.693G>A, NM_001459.3:c.693G>A, XM_011526676.4:c.514G>A, XM_011526676.3:c.514G>A, XM_011526676.2:c.514G>A, XM_011526676.1:c.514G>A, XM_006723116.4:c.554G>A, XM_006723116.3:c.554G>A, XM_006723116.2:c.554G>A, XM_006723116.1:c.683G>A, XM_011526675.3:c.514G>A, XM_011526675.2:c.514G>A, XM_011526675.1:c.514G>A, XM_011526677.3:c.514G>A, XM_011526677.2:c.514G>A, XM_011526677.1:c.514G>A, XM_011526678.3:c.460G>A, XM_011526678.2:c.460G>A, XM_011526678.1:c.460G>A, NM_001204502.2:c.693G>A, NM_001204502.1:c.693G>A, NM_001278637.2:c.447G>A, NM_001278637.1:c.447G>A, NM_001278638.2:c.447G>A, NM_001278638.1:c.447G>A, NM_001204503.2:c.693G>A, NM_001204503.1:c.693G>A, XM_047438522.1:c.554G>A, XM_047438523.1:c.554G>A, XM_047438520.1:c.693G>A, XP_011524978.1:p.Ala172Thr, XP_006723179.2:p.Cys185Tyr, XP_011524977.1:p.Ala172Thr, XP_011524979.1:p.Ala172Thr, XP_011524980.1:p.Ala154Thr, XP_047294478.1:p.Cys185Tyr, XP_047294479.1:p.Cys185Tyr

      3.

      rs1477105731 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>T [Show Flanks]
        Chromosome:
        19:49476527 (GRCh38)
        19:49979784 (GRCh37)
        Canonical SPDI:
        NC_000019.10:49476526:G:T
        Gene:
        FLT3LG (Varview)
        Functional Consequence:
        synonymous_variant,coding_sequence_variant
        Validated:
        by frequency,by alfa
        MAF:
        T=0./0 (ALFA)
        T=0.000004/1 (TOPMED)
        HGVS:
        NC_000019.10:g.49476527G>T, NC_000019.9:g.49979784G>T, NM_001459.4:c.303G>T, NM_001459.3:c.303G>T, XM_011526676.4:c.303G>T, XM_011526676.3:c.303G>T, XM_011526676.2:c.303G>T, XM_011526676.1:c.303G>T, XM_006723116.4:c.303G>T, XM_006723116.3:c.303G>T, XM_006723116.2:c.303G>T, XM_006723116.1:c.432G>T, XM_011526675.3:c.303G>T, XM_011526675.2:c.303G>T, XM_011526675.1:c.303G>T, XM_011526677.3:c.303G>T, XM_011526677.2:c.303G>T, XM_011526677.1:c.303G>T, XM_011526678.3:c.303G>T, XM_011526678.2:c.303G>T, XM_011526678.1:c.303G>T, XM_011526680.3:c.303G>T, XM_011526680.2:c.303G>T, XM_011526680.1:c.303G>T, NM_001204502.2:c.303G>T, NM_001204502.1:c.303G>T, NM_001278637.2:c.57G>T, NM_001278637.1:c.57G>T, NM_001278638.2:c.57G>T, NM_001278638.1:c.57G>T, NM_001204503.2:c.303G>T, NM_001204503.1:c.303G>T, XM_047438522.1:c.303G>T, XM_047438519.1:c.303G>T, XM_047438523.1:c.303G>T, XM_047438520.1:c.303G>T, XM_047438521.1:c.303G>T

        4.

        rs1473621169 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>G,T [Show Flanks]
          Chromosome:
          19:49476500 (GRCh38)
          19:49979757 (GRCh37)
          Canonical SPDI:
          NC_000019.10:49476499:C:G,NC_000019.10:49476499:C:T
          Gene:
          FLT3LG (Varview)
          Functional Consequence:
          synonymous_variant,coding_sequence_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          G=0.000028/1 (ALFA)
          T=0.000008/2 (TOPMED)
          T=0.00002/5 (GnomAD_exomes)
          HGVS:
          NC_000019.10:g.49476500C>G, NC_000019.10:g.49476500C>T, NC_000019.9:g.49979757C>G, NC_000019.9:g.49979757C>T, NM_001459.4:c.276C>G, NM_001459.4:c.276C>T, NM_001459.3:c.276C>G, NM_001459.3:c.276C>T, XM_011526676.4:c.276C>G, XM_011526676.4:c.276C>T, XM_011526676.3:c.276C>G, XM_011526676.3:c.276C>T, XM_011526676.2:c.276C>G, XM_011526676.2:c.276C>T, XM_011526676.1:c.276C>G, XM_011526676.1:c.276C>T, XM_006723116.4:c.276C>G, XM_006723116.4:c.276C>T, XM_006723116.3:c.276C>G, XM_006723116.3:c.276C>T, XM_006723116.2:c.276C>G, XM_006723116.2:c.276C>T, XM_006723116.1:c.405C>G, XM_006723116.1:c.405C>T, XM_011526675.3:c.276C>G, XM_011526675.3:c.276C>T, XM_011526675.2:c.276C>G, XM_011526675.2:c.276C>T, XM_011526675.1:c.276C>G, XM_011526675.1:c.276C>T, XM_011526677.3:c.276C>G, XM_011526677.3:c.276C>T, XM_011526677.2:c.276C>G, XM_011526677.2:c.276C>T, XM_011526677.1:c.276C>G, XM_011526677.1:c.276C>T, XM_011526678.3:c.276C>G, XM_011526678.3:c.276C>T, XM_011526678.2:c.276C>G, XM_011526678.2:c.276C>T, XM_011526678.1:c.276C>G, XM_011526678.1:c.276C>T, XM_011526680.3:c.276C>G, XM_011526680.3:c.276C>T, XM_011526680.2:c.276C>G, XM_011526680.2:c.276C>T, XM_011526680.1:c.276C>G, XM_011526680.1:c.276C>T, NM_001204502.2:c.276C>G, NM_001204502.2:c.276C>T, NM_001204502.1:c.276C>G, NM_001204502.1:c.276C>T, NM_001278637.2:c.30C>G, NM_001278637.2:c.30C>T, NM_001278637.1:c.30C>G, NM_001278637.1:c.30C>T, NM_001278638.2:c.30C>G, NM_001278638.2:c.30C>T, NM_001278638.1:c.30C>G, NM_001278638.1:c.30C>T, NM_001204503.2:c.276C>G, NM_001204503.2:c.276C>T, NM_001204503.1:c.276C>G, NM_001204503.1:c.276C>T, XM_047438522.1:c.276C>G, XM_047438522.1:c.276C>T, XM_047438519.1:c.276C>G, XM_047438519.1:c.276C>T, XM_047438523.1:c.276C>G, XM_047438523.1:c.276C>T, XM_047438520.1:c.276C>G, XM_047438520.1:c.276C>T, XM_047438521.1:c.276C>G, XM_047438521.1:c.276C>T

          5.

          rs1470448364 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>A [Show Flanks]
            Chromosome:
            19:49486187 (GRCh38)
            19:49989444 (GRCh37)
            Canonical SPDI:
            NC_000019.10:49486186:G:A
            Gene:
            FLT3LG (Varview), RPL13A (Varview)
            Functional Consequence:
            2KB_upstream_variant,genic_downstream_transcript_variant,coding_sequence_variant,synonymous_variant,upstream_transcript_variant,3_prime_UTR_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            A=0./0 (ALFA)
            A=0.000007/1 (GnomAD)
            A=0.000008/2 (TOPMED)
            HGVS:

            6.

            rs1463648878 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>G [Show Flanks]
              Chromosome:
              19:49476440 (GRCh38)
              19:49979697 (GRCh37)
              Canonical SPDI:
              NC_000019.10:49476439:C:G
              Gene:
              FLT3LG (Varview)
              Functional Consequence:
              5_prime_UTR_variant,coding_sequence_variant,synonymous_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              G=0./0 (ALFA)
              G=0.000014/2 (GnomAD)
              G=0.000019/5 (TOPMED)
              HGVS:
              NC_000019.10:g.49476440C>G, NC_000019.9:g.49979697C>G, NM_001459.4:c.216C>G, NM_001459.3:c.216C>G, XM_011526676.4:c.216C>G, XM_011526676.3:c.216C>G, XM_011526676.2:c.216C>G, XM_011526676.1:c.216C>G, XM_006723116.4:c.216C>G, XM_006723116.3:c.216C>G, XM_006723116.2:c.216C>G, XM_006723116.1:c.345C>G, XM_011526675.3:c.216C>G, XM_011526675.2:c.216C>G, XM_011526675.1:c.216C>G, XM_011526677.3:c.216C>G, XM_011526677.2:c.216C>G, XM_011526677.1:c.216C>G, XM_011526678.3:c.216C>G, XM_011526678.2:c.216C>G, XM_011526678.1:c.216C>G, XM_011526680.3:c.216C>G, XM_011526680.2:c.216C>G, XM_011526680.1:c.216C>G, NM_001204502.2:c.216C>G, NM_001204502.1:c.216C>G, NM_001278637.2:c.-31C>G, NM_001278637.1:c.-31C>G, NM_001278638.2:c.-31C>G, NM_001278638.1:c.-31C>G, NM_001204503.2:c.216C>G, NM_001204503.1:c.216C>G, XM_047438522.1:c.216C>G, XM_047438519.1:c.216C>G, XM_047438523.1:c.216C>G, XM_047438520.1:c.216C>G, XM_047438521.1:c.216C>G

              7.

              rs1462712837 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>G,T [Show Flanks]
                Chromosome:
                19:49479005 (GRCh38)
                19:49982262 (GRCh37)
                Canonical SPDI:
                NC_000019.10:49479004:C:G,NC_000019.10:49479004:C:T
                Gene:
                FLT3LG (Varview)
                Functional Consequence:
                intron_variant,coding_sequence_variant,missense_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                T=0./0 (ALFA)
                HGVS:
                NC_000019.10:g.49479005C>G, NC_000019.10:g.49479005C>T, NC_000019.9:g.49982262C>G, NC_000019.9:g.49982262C>T, NM_001459.4:c.439C>G, NM_001459.4:c.439C>T, NM_001459.3:c.439C>G, NM_001459.3:c.439C>T, XM_011526676.4:c.439C>G, XM_011526676.4:c.439C>T, XM_011526676.3:c.439C>G, XM_011526676.3:c.439C>T, XM_011526676.2:c.439C>G, XM_011526676.2:c.439C>T, XM_011526676.1:c.439C>G, XM_011526676.1:c.439C>T, XM_011526675.3:c.439C>G, XM_011526675.3:c.439C>T, XM_011526675.2:c.439C>G, XM_011526675.2:c.439C>T, XM_011526675.1:c.439C>G, XM_011526675.1:c.439C>T, XM_011526677.3:c.439C>G, XM_011526677.3:c.439C>T, XM_011526677.2:c.439C>G, XM_011526677.2:c.439C>T, XM_011526677.1:c.439C>G, XM_011526677.1:c.439C>T, XM_011526678.3:c.385C>G, XM_011526678.3:c.385C>T, XM_011526678.2:c.385C>G, XM_011526678.2:c.385C>T, XM_011526678.1:c.385C>G, XM_011526678.1:c.385C>T, NM_001204502.2:c.439C>G, NM_001204502.2:c.439C>T, NM_001204502.1:c.439C>G, NM_001204502.1:c.439C>T, NM_001278637.2:c.193C>G, NM_001278637.2:c.193C>T, NM_001278637.1:c.193C>G, NM_001278637.1:c.193C>T, NM_001278638.2:c.193C>G, NM_001278638.2:c.193C>T, NM_001278638.1:c.193C>G, NM_001278638.1:c.193C>T, NM_001204503.2:c.439C>G, NM_001204503.2:c.439C>T, NM_001204503.1:c.439C>G, NM_001204503.1:c.439C>T, XM_047438519.1:c.439C>G, XM_047438519.1:c.439C>T, XM_047438520.1:c.439C>G, XM_047438520.1:c.439C>T, NP_001450.2:p.Arg147Gly, NP_001450.2:p.Arg147Cys, XP_011524978.1:p.Arg147Gly, XP_011524978.1:p.Arg147Cys, XP_011524977.1:p.Arg147Gly, XP_011524977.1:p.Arg147Cys, XP_011524979.1:p.Arg147Gly, XP_011524979.1:p.Arg147Cys, XP_011524980.1:p.Arg129Gly, XP_011524980.1:p.Arg129Cys, NP_001191431.1:p.Arg147Gly, NP_001191431.1:p.Arg147Cys, NP_001265566.1:p.Arg65Gly, NP_001265566.1:p.Arg65Cys, NP_001265567.1:p.Arg65Gly, NP_001265567.1:p.Arg65Cys, NP_001191432.1:p.Arg147Gly, NP_001191432.1:p.Arg147Cys, XP_047294475.1:p.Arg147Gly, XP_047294475.1:p.Arg147Cys, XP_047294476.1:p.Arg147Gly, XP_047294476.1:p.Arg147Cys

                8.

                rs1461617324 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>A [Show Flanks]
                  Chromosome:
                  19:49480588 (GRCh38)
                  19:49983845 (GRCh37)
                  Canonical SPDI:
                  NC_000019.10:49480587:G:A
                  Gene:
                  FLT3LG (Varview)
                  Functional Consequence:
                  synonymous_variant,intron_variant,coding_sequence_variant,missense_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  A=0./0 (ALFA)
                  A=0.000004/1 (TOPMED)
                  A=0.000014/2 (GnomAD)
                  HGVS:
                  NC_000019.10:g.49480588G>A, NC_000019.9:g.49983845G>A, NM_001459.4:c.697G>A, NM_001459.3:c.697G>A, XM_011526676.4:c.518G>A, XM_011526676.3:c.518G>A, XM_011526676.2:c.518G>A, XM_011526676.1:c.518G>A, XM_006723116.4:c.558G>A, XM_006723116.3:c.558G>A, XM_006723116.2:c.558G>A, XM_006723116.1:c.687G>A, XM_011526675.3:c.518G>A, XM_011526675.2:c.518G>A, XM_011526675.1:c.518G>A, XM_011526677.3:c.518G>A, XM_011526677.2:c.518G>A, XM_011526677.1:c.518G>A, XM_011526678.3:c.464G>A, XM_011526678.2:c.464G>A, XM_011526678.1:c.464G>A, NM_001204502.2:c.697G>A, NM_001204502.1:c.697G>A, NM_001278637.2:c.451G>A, NM_001278637.1:c.451G>A, NM_001278638.2:c.451G>A, NM_001278638.1:c.451G>A, NM_001204503.2:c.697G>A, NM_001204503.1:c.697G>A, XM_047438522.1:c.558G>A, XM_047438523.1:c.558G>A, XM_047438520.1:c.697G>A, NP_001450.2:p.Val233Met, XP_011524978.1:p.Cys173Tyr, XP_011524977.1:p.Cys173Tyr, XP_011524979.1:p.Cys173Tyr, XP_011524980.1:p.Cys155Tyr, NP_001191431.1:p.Val233Met, NP_001265566.1:p.Val151Met, NP_001265567.1:p.Val151Met, NP_001191432.1:p.Val233Met, XP_047294476.1:p.Val233Met

                  9.

                  rs1460905765 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>G [Show Flanks]
                    Chromosome:
                    19:49480599 (GRCh38)
                    19:49983856 (GRCh37)
                    Canonical SPDI:
                    NC_000019.10:49480598:A:G
                    Gene:
                    FLT3LG (Varview)
                    Functional Consequence:
                    stop_lost,coding_sequence_variant,intron_variant,missense_variant,terminator_codon_variant
                    Validated:
                    by frequency
                    MAF:
                    G=0.000004/1 (GnomAD_exomes)
                    HGVS:
                    NC_000019.10:g.49480599A>G, NC_000019.9:g.49983856A>G, NM_001459.4:c.708A>G, NM_001459.3:c.708A>G, XM_011526676.4:c.529A>G, XM_011526676.3:c.529A>G, XM_011526676.2:c.529A>G, XM_011526676.1:c.529A>G, XM_006723116.4:c.569A>G, XM_006723116.3:c.569A>G, XM_006723116.2:c.569A>G, XM_006723116.1:c.698A>G, XM_011526675.3:c.529A>G, XM_011526675.2:c.529A>G, XM_011526675.1:c.529A>G, XM_011526677.3:c.529A>G, XM_011526677.2:c.529A>G, XM_011526677.1:c.529A>G, XM_011526678.3:c.475A>G, XM_011526678.2:c.475A>G, XM_011526678.1:c.475A>G, NM_001204502.2:c.708A>G, NM_001204502.1:c.708A>G, NM_001278637.2:c.462A>G, NM_001278637.1:c.462A>G, NM_001278638.2:c.462A>G, NM_001278638.1:c.462A>G, NM_001204503.2:c.708A>G, NM_001204503.1:c.708A>G, XM_047438522.1:c.569A>G, XM_047438523.1:c.569A>G, XM_047438520.1:c.708A>G, NP_001450.2:p.Ter236Trp, XP_011524978.1:p.Thr177Ala, XP_006723179.2:p.Asp190Gly, XP_011524977.1:p.Thr177Ala, XP_011524979.1:p.Thr177Ala, XP_011524980.1:p.Thr159Ala, NP_001191431.1:p.Ter236Trp, NP_001265566.1:p.Ter154Trp, NP_001265567.1:p.Ter154Trp, NP_001191432.1:p.Ter236Trp, XP_047294478.1:p.Asp190Gly, XP_047294479.1:p.Asp190Gly, XP_047294476.1:p.Ter236Trp

                    10.

                    rs1456146133 has merged into rs750620711 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      CTG>-,CTGCTG [Show Flanks]
                      Chromosome:
                      19:49475715 (GRCh38)
                      19:49978972 (GRCh37)
                      Canonical SPDI:
                      NC_000019.10:49475702:CTGCTGCTGCTGCTG:CTGCTGCTGCTG,NC_000019.10:49475702:CTGCTGCTGCTGCTG:CTGCTGCTGCTGCTGCTG
                      Gene:
                      FLT3LG (Varview)
                      Functional Consequence:
                      coding_sequence_variant,5_prime_UTR_variant,inframe_insertion,inframe_deletion
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      CTGCTGCTGCTG=0.002062/43 (ALFA)
                      -=0.000007/1 (GnomAD)
                      -=0.000988/118 (ExAC)
                      HGVS:
                      NC_000019.10:g.49475703CTG[4], NC_000019.10:g.49475703CTG[6], NC_000019.9:g.49978960CTG[4], NC_000019.9:g.49978960CTG[6], NM_001459.4:c.46CTG[4], NM_001459.4:c.46CTG[6], NM_001459.3:c.46CTG[4], NM_001459.3:c.46CTG[6], XM_011526676.4:c.46CTG[4], XM_011526676.4:c.46CTG[6], XM_011526676.3:c.46CTG[4], XM_011526676.3:c.46CTG[6], XM_011526676.2:c.46CTG[4], XM_011526676.2:c.46CTG[6], XM_011526676.1:c.46CTG[4], XM_011526676.1:c.46CTG[6], XM_006723116.4:c.46CTG[4], XM_006723116.4:c.46CTG[6], XM_006723116.3:c.46CTG[4], XM_006723116.3:c.46CTG[6], XM_006723116.2:c.46CTG[4], XM_006723116.2:c.46CTG[6], XM_006723116.1:c.175CTG[4], XM_006723116.1:c.175CTG[6], XM_011526675.3:c.46CTG[4], XM_011526675.3:c.46CTG[6], XM_011526675.2:c.46CTG[4], XM_011526675.2:c.46CTG[6], XM_011526675.1:c.46CTG[4], XM_011526675.1:c.46CTG[6], XM_011526677.3:c.46CTG[4], XM_011526677.3:c.46CTG[6], XM_011526677.2:c.46CTG[4], XM_011526677.2:c.46CTG[6], XM_011526677.1:c.46CTG[4], XM_011526677.1:c.46CTG[6], XM_011526678.3:c.46CTG[4], XM_011526678.3:c.46CTG[6], XM_011526678.2:c.46CTG[4], XM_011526678.2:c.46CTG[6], XM_011526678.1:c.46CTG[4], XM_011526678.1:c.46CTG[6], XM_011526680.3:c.46CTG[4], XM_011526680.3:c.46CTG[6], XM_011526680.2:c.46CTG[4], XM_011526680.2:c.46CTG[6], XM_011526680.1:c.46CTG[4], XM_011526680.1:c.46CTG[6], NM_001204502.2:c.46CTG[4], NM_001204502.2:c.46CTG[6], NM_001204502.1:c.46CTG[4], NM_001204502.1:c.46CTG[6], NM_001278637.2:c.-229CTG[4], NM_001278637.2:c.-229CTG[6], NM_001278637.1:c.-229CTG[4], NM_001278637.1:c.-229CTG[6], NM_001278638.2:c.-201CTG[4], NM_001278638.2:c.-201CTG[6], NM_001278638.1:c.-201CTG[4], NM_001278638.1:c.-201CTG[6], NM_001204503.2:c.46CTG[4], NM_001204503.2:c.46CTG[6], NM_001204503.1:c.46CTG[4], NM_001204503.1:c.46CTG[6], XM_047438522.1:c.46CTG[4], XM_047438522.1:c.46CTG[6], XM_047438519.1:c.46CTG[4], XM_047438519.1:c.46CTG[6], XM_047438523.1:c.46CTG[4], XM_047438523.1:c.46CTG[6], XM_047438520.1:c.46CTG[4], XM_047438520.1:c.46CTG[6], XM_047438521.1:c.46CTG[4], XM_047438521.1:c.46CTG[6], NP_001450.2:p.Leu20del, NP_001450.2:p.Leu20dup, XP_011524978.1:p.Leu20del, XP_011524978.1:p.Leu20dup, XP_006723179.2:p.Leu20del, XP_006723179.2:p.Leu20dup, XP_011524977.1:p.Leu20del, XP_011524977.1:p.Leu20dup, XP_011524979.1:p.Leu20del, XP_011524979.1:p.Leu20dup, XP_011524980.1:p.Leu20del, XP_011524980.1:p.Leu20dup, XP_011524982.1:p.Leu20del, XP_011524982.1:p.Leu20dup, NP_001191431.1:p.Leu20del, NP_001191431.1:p.Leu20dup, NP_001191432.1:p.Leu20del, NP_001191432.1:p.Leu20dup, XP_047294478.1:p.Leu20del, XP_047294478.1:p.Leu20dup, XP_047294475.1:p.Leu20del, XP_047294475.1:p.Leu20dup, XP_047294479.1:p.Leu20del, XP_047294479.1:p.Leu20dup, XP_047294476.1:p.Leu20del, XP_047294476.1:p.Leu20dup, XP_047294477.1:p.Leu20del, XP_047294477.1:p.Leu20dup

                      11.

                      rs1452719289 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>A,T [Show Flanks]
                        Chromosome:
                        19:49476511 (GRCh38)
                        19:49979768 (GRCh37)
                        Canonical SPDI:
                        NC_000019.10:49476510:G:A,NC_000019.10:49476510:G:T
                        Gene:
                        FLT3LG (Varview)
                        Functional Consequence:
                        coding_sequence_variant,missense_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        A=0./0 (ALFA)
                        A=0.000007/1 (GnomAD)
                        HGVS:
                        NC_000019.10:g.49476511G>A, NC_000019.10:g.49476511G>T, NC_000019.9:g.49979768G>A, NC_000019.9:g.49979768G>T, NM_001459.4:c.287G>A, NM_001459.4:c.287G>T, NM_001459.3:c.287G>A, NM_001459.3:c.287G>T, XM_011526676.4:c.287G>A, XM_011526676.4:c.287G>T, XM_011526676.3:c.287G>A, XM_011526676.3:c.287G>T, XM_011526676.2:c.287G>A, XM_011526676.2:c.287G>T, XM_011526676.1:c.287G>A, XM_011526676.1:c.287G>T, XM_006723116.4:c.287G>A, XM_006723116.4:c.287G>T, XM_006723116.3:c.287G>A, XM_006723116.3:c.287G>T, XM_006723116.2:c.287G>A, XM_006723116.2:c.287G>T, XM_006723116.1:c.416G>A, XM_006723116.1:c.416G>T, XM_011526675.3:c.287G>A, XM_011526675.3:c.287G>T, XM_011526675.2:c.287G>A, XM_011526675.2:c.287G>T, XM_011526675.1:c.287G>A, XM_011526675.1:c.287G>T, XM_011526677.3:c.287G>A, XM_011526677.3:c.287G>T, XM_011526677.2:c.287G>A, XM_011526677.2:c.287G>T, XM_011526677.1:c.287G>A, XM_011526677.1:c.287G>T, XM_011526678.3:c.287G>A, XM_011526678.3:c.287G>T, XM_011526678.2:c.287G>A, XM_011526678.2:c.287G>T, XM_011526678.1:c.287G>A, XM_011526678.1:c.287G>T, XM_011526680.3:c.287G>A, XM_011526680.3:c.287G>T, XM_011526680.2:c.287G>A, XM_011526680.2:c.287G>T, XM_011526680.1:c.287G>A, XM_011526680.1:c.287G>T, NM_001204502.2:c.287G>A, NM_001204502.2:c.287G>T, NM_001204502.1:c.287G>A, NM_001204502.1:c.287G>T, NM_001278637.2:c.41G>A, NM_001278637.2:c.41G>T, NM_001278637.1:c.41G>A, NM_001278637.1:c.41G>T, NM_001278638.2:c.41G>A, NM_001278638.2:c.41G>T, NM_001278638.1:c.41G>A, NM_001278638.1:c.41G>T, NM_001204503.2:c.287G>A, NM_001204503.2:c.287G>T, NM_001204503.1:c.287G>A, NM_001204503.1:c.287G>T, XM_047438522.1:c.287G>A, XM_047438522.1:c.287G>T, XM_047438519.1:c.287G>A, XM_047438519.1:c.287G>T, XM_047438523.1:c.287G>A, XM_047438523.1:c.287G>T, XM_047438520.1:c.287G>A, XM_047438520.1:c.287G>T, XM_047438521.1:c.287G>A, XM_047438521.1:c.287G>T, NP_001450.2:p.Gly96Asp, NP_001450.2:p.Gly96Val, XP_011524978.1:p.Gly96Asp, XP_011524978.1:p.Gly96Val, XP_006723179.2:p.Gly96Asp, XP_006723179.2:p.Gly96Val, XP_011524977.1:p.Gly96Asp, XP_011524977.1:p.Gly96Val, XP_011524979.1:p.Gly96Asp, XP_011524979.1:p.Gly96Val, XP_011524980.1:p.Gly96Asp, XP_011524980.1:p.Gly96Val, XP_011524982.1:p.Gly96Asp, XP_011524982.1:p.Gly96Val, NP_001191431.1:p.Gly96Asp, NP_001191431.1:p.Gly96Val, NP_001265566.1:p.Gly14Asp, NP_001265566.1:p.Gly14Val, NP_001265567.1:p.Gly14Asp, NP_001265567.1:p.Gly14Val, NP_001191432.1:p.Gly96Asp, NP_001191432.1:p.Gly96Val, XP_047294478.1:p.Gly96Asp, XP_047294478.1:p.Gly96Val, XP_047294475.1:p.Gly96Asp, XP_047294475.1:p.Gly96Val, XP_047294479.1:p.Gly96Asp, XP_047294479.1:p.Gly96Val, XP_047294476.1:p.Gly96Asp, XP_047294476.1:p.Gly96Val, XP_047294477.1:p.Gly96Asp, XP_047294477.1:p.Gly96Val

                        12.

                        rs1452404469 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          19:49480618 (GRCh38)
                          19:49983875 (GRCh37)
                          Canonical SPDI:
                          NC_000019.10:49480617:C:T
                          Gene:
                          FLT3LG (Varview)
                          Functional Consequence:
                          3_prime_UTR_variant,coding_sequence_variant,synonymous_variant,intron_variant,missense_variant
                          Validated:
                          by frequency
                          MAF:
                          T=0.000008/2 (GnomAD_exomes)
                          HGVS:
                          NC_000019.10:g.49480618C>T, NC_000019.9:g.49983875C>T, NM_001459.4:c.*19C>T, NM_001459.3:c.*19C>T, XM_011526676.4:c.548C>T, XM_011526676.3:c.548C>T, XM_011526676.2:c.548C>T, XM_011526676.1:c.548C>T, XM_006723116.4:c.588C>T, XM_006723116.3:c.588C>T, XM_006723116.2:c.588C>T, XM_006723116.1:c.717C>T, XM_011526675.3:c.548C>T, XM_011526675.2:c.548C>T, XM_011526675.1:c.548C>T, XM_011526677.3:c.548C>T, XM_011526677.2:c.548C>T, XM_011526677.1:c.548C>T, XM_011526678.3:c.494C>T, XM_011526678.2:c.494C>T, XM_011526678.1:c.494C>T, NM_001204502.2:c.*19C>T, NM_001204502.1:c.*19C>T, NM_001278637.2:c.*19C>T, NM_001278637.1:c.*19C>T, NM_001278638.2:c.*19C>T, NM_001278638.1:c.*19C>T, NM_001204503.2:c.*19C>T, NM_001204503.1:c.*19C>T, XM_047438522.1:c.588C>T, XM_047438523.1:c.588C>T, XM_047438520.1:c.*19C>T, XP_011524978.1:p.Pro183Leu, XP_011524977.1:p.Pro183Leu, XP_011524979.1:p.Pro183Leu, XP_011524980.1:p.Pro165Leu

                          13.

                          rs1451163505 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>T [Show Flanks]
                            Chromosome:
                            19:49478985 (GRCh38)
                            19:49982242 (GRCh37)
                            Canonical SPDI:
                            NC_000019.10:49478984:C:T
                            Gene:
                            FLT3LG (Varview)
                            Functional Consequence:
                            intron_variant,coding_sequence_variant,missense_variant
                            Validated:
                            by frequency,by cluster
                            MAF:
                            T=0.00025/4 (TOMMO)
                            HGVS:
                            NC_000019.10:g.49478985C>T, NC_000019.9:g.49982242C>T, NM_001459.4:c.419C>T, NM_001459.3:c.419C>T, XM_011526676.4:c.419C>T, XM_011526676.3:c.419C>T, XM_011526676.2:c.419C>T, XM_011526676.1:c.419C>T, XM_011526675.3:c.419C>T, XM_011526675.2:c.419C>T, XM_011526675.1:c.419C>T, XM_011526677.3:c.419C>T, XM_011526677.2:c.419C>T, XM_011526677.1:c.419C>T, XM_011526678.3:c.365C>T, XM_011526678.2:c.365C>T, XM_011526678.1:c.365C>T, NM_001204502.2:c.419C>T, NM_001204502.1:c.419C>T, NM_001278637.2:c.173C>T, NM_001278637.1:c.173C>T, NM_001278638.2:c.173C>T, NM_001278638.1:c.173C>T, NM_001204503.2:c.419C>T, NM_001204503.1:c.419C>T, XM_047438519.1:c.419C>T, XM_047438520.1:c.419C>T, NP_001450.2:p.Ala140Val, XP_011524978.1:p.Ala140Val, XP_011524977.1:p.Ala140Val, XP_011524979.1:p.Ala140Val, XP_011524980.1:p.Ala122Val, NP_001191431.1:p.Ala140Val, NP_001265566.1:p.Ala58Val, NP_001265567.1:p.Ala58Val, NP_001191432.1:p.Ala140Val, XP_047294475.1:p.Ala140Val, XP_047294476.1:p.Ala140Val

                            14.

                            rs1444695355 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A [Show Flanks]
                              Chromosome:
                              19:49475761 (GRCh38)
                              19:49979018 (GRCh37)
                              Canonical SPDI:
                              NC_000019.10:49475760:G:A
                              Gene:
                              FLT3LG (Varview)
                              Functional Consequence:
                              5_prime_UTR_variant,coding_sequence_variant,missense_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.49475761G>A, NC_000019.9:g.49979018G>A, NM_001459.4:c.104G>A, NM_001459.3:c.104G>A, XM_011526676.4:c.104G>A, XM_011526676.3:c.104G>A, XM_011526676.2:c.104G>A, XM_011526676.1:c.104G>A, XM_006723116.4:c.104G>A, XM_006723116.3:c.104G>A, XM_006723116.2:c.104G>A, XM_006723116.1:c.233G>A, XM_011526675.3:c.104G>A, XM_011526675.2:c.104G>A, XM_011526675.1:c.104G>A, XM_011526677.3:c.104G>A, XM_011526677.2:c.104G>A, XM_011526677.1:c.104G>A, XM_011526678.3:c.104G>A, XM_011526678.2:c.104G>A, XM_011526678.1:c.104G>A, XM_011526680.3:c.104G>A, XM_011526680.2:c.104G>A, XM_011526680.1:c.104G>A, NM_001204502.2:c.104G>A, NM_001204502.1:c.104G>A, NM_001278637.2:c.-171G>A, NM_001278637.1:c.-171G>A, NM_001278638.2:c.-143G>A, NM_001278638.1:c.-143G>A, NM_001204503.2:c.104G>A, NM_001204503.1:c.104G>A, XM_047438522.1:c.104G>A, XM_047438519.1:c.104G>A, XM_047438523.1:c.104G>A, XM_047438520.1:c.104G>A, XM_047438521.1:c.104G>A, NP_001450.2:p.Ser35Asn, XP_011524978.1:p.Ser35Asn, XP_006723179.2:p.Ser35Asn, XP_011524977.1:p.Ser35Asn, XP_011524979.1:p.Ser35Asn, XP_011524980.1:p.Ser35Asn, XP_011524982.1:p.Ser35Asn, NP_001191431.1:p.Ser35Asn, NP_001191432.1:p.Ser35Asn, XP_047294478.1:p.Ser35Asn, XP_047294475.1:p.Ser35Asn, XP_047294479.1:p.Ser35Asn, XP_047294476.1:p.Ser35Asn, XP_047294477.1:p.Ser35Asn

                              15.

                              rs1439066393 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                TCC>- [Show Flanks]
                                Chromosome:
                                19:49475772 (GRCh38)
                                19:49979029 (GRCh37)
                                Canonical SPDI:
                                NC_000019.10:49475767:CTCCTCC:CTCC
                                Gene:
                                FLT3LG (Varview)
                                Functional Consequence:
                                inframe_deletion,5_prime_UTR_variant,coding_sequence_variant
                                Validated:
                                by frequency
                                MAF:
                                -=0.000004/1 (GnomAD_exomes)
                                HGVS:
                                NC_000019.10:g.49475769TCC[1], NC_000019.9:g.49979026TCC[1], NM_001459.4:c.112TCC[1], NM_001459.3:c.112TCC[1], XM_011526676.4:c.112TCC[1], XM_011526676.3:c.112TCC[1], XM_011526676.2:c.112TCC[1], XM_011526676.1:c.112TCC[1], XM_006723116.4:c.112TCC[1], XM_006723116.3:c.112TCC[1], XM_006723116.2:c.112TCC[1], XM_006723116.1:c.241TCC[1], XM_011526675.3:c.112TCC[1], XM_011526675.2:c.112TCC[1], XM_011526675.1:c.112TCC[1], XM_011526677.3:c.112TCC[1], XM_011526677.2:c.112TCC[1], XM_011526677.1:c.112TCC[1], XM_011526678.3:c.112TCC[1], XM_011526678.2:c.112TCC[1], XM_011526678.1:c.112TCC[1], XM_011526680.3:c.112TCC[1], XM_011526680.2:c.112TCC[1], XM_011526680.1:c.112TCC[1], NM_001204502.2:c.112TCC[1], NM_001204502.1:c.112TCC[1], NM_001278637.2:c.-163TCC[1], NM_001278637.1:c.-163TCC[1], NM_001278638.2:c.-135TCC[1], NM_001278638.1:c.-135TCC[1], NM_001204503.2:c.112TCC[1], NM_001204503.1:c.112TCC[1], XM_047438522.1:c.112TCC[1], XM_047438519.1:c.112TCC[1], XM_047438523.1:c.112TCC[1], XM_047438520.1:c.112TCC[1], XM_047438521.1:c.112TCC[1], NP_001450.2:p.Ser39del, XP_011524978.1:p.Ser39del, XP_006723179.2:p.Ser39del, XP_011524977.1:p.Ser39del, XP_011524979.1:p.Ser39del, XP_011524980.1:p.Ser39del, XP_011524982.1:p.Ser39del, NP_001191431.1:p.Ser39del, NP_001191432.1:p.Ser39del, XP_047294478.1:p.Ser39del, XP_047294475.1:p.Ser39del, XP_047294479.1:p.Ser39del, XP_047294476.1:p.Ser39del, XP_047294477.1:p.Ser39del

                                16.

                                rs1413770713 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  19:49475781 (GRCh38)
                                  19:49979038 (GRCh37)
                                  Canonical SPDI:
                                  NC_000019.10:49475780:G:A
                                  Gene:
                                  FLT3LG (Varview)
                                  Functional Consequence:
                                  missense_variant,5_prime_UTR_variant,coding_sequence_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  A=0./0 (ALFA)
                                  A=0.000007/1 (GnomAD)
                                  HGVS:
                                  NC_000019.10:g.49475781G>A, NC_000019.9:g.49979038G>A, NM_001459.4:c.124G>A, NM_001459.3:c.124G>A, XM_011526676.4:c.124G>A, XM_011526676.3:c.124G>A, XM_011526676.2:c.124G>A, XM_011526676.1:c.124G>A, XM_006723116.4:c.124G>A, XM_006723116.3:c.124G>A, XM_006723116.2:c.124G>A, XM_006723116.1:c.253G>A, XM_011526675.3:c.124G>A, XM_011526675.2:c.124G>A, XM_011526675.1:c.124G>A, XM_011526677.3:c.124G>A, XM_011526677.2:c.124G>A, XM_011526677.1:c.124G>A, XM_011526678.3:c.124G>A, XM_011526678.2:c.124G>A, XM_011526678.1:c.124G>A, XM_011526680.3:c.124G>A, XM_011526680.2:c.124G>A, XM_011526680.1:c.124G>A, NM_001204502.2:c.124G>A, NM_001204502.1:c.124G>A, NM_001278637.2:c.-151G>A, NM_001278637.1:c.-151G>A, NM_001278638.2:c.-123G>A, NM_001278638.1:c.-123G>A, NM_001204503.2:c.124G>A, NM_001204503.1:c.124G>A, XM_047438522.1:c.124G>A, XM_047438519.1:c.124G>A, XM_047438523.1:c.124G>A, XM_047438520.1:c.124G>A, XM_047438521.1:c.124G>A, NP_001450.2:p.Ala42Thr, XP_011524978.1:p.Ala42Thr, XP_006723179.2:p.Ala42Thr, XP_011524977.1:p.Ala42Thr, XP_011524979.1:p.Ala42Thr, XP_011524980.1:p.Ala42Thr, XP_011524982.1:p.Ala42Thr, NP_001191431.1:p.Ala42Thr, NP_001191432.1:p.Ala42Thr, XP_047294478.1:p.Ala42Thr, XP_047294475.1:p.Ala42Thr, XP_047294479.1:p.Ala42Thr, XP_047294476.1:p.Ala42Thr, XP_047294477.1:p.Ala42Thr

                                  17.

                                  rs1413372247 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A [Show Flanks]
                                    Chromosome:
                                    19:49475734 (GRCh38)
                                    19:49978991 (GRCh37)
                                    Canonical SPDI:
                                    NC_000019.10:49475733:G:A
                                    Gene:
                                    FLT3LG (Varview)
                                    Functional Consequence:
                                    missense_variant,5_prime_UTR_variant,coding_sequence_variant
                                    Validated:
                                    by frequency
                                    MAF:
                                    A=0.000004/1 (GnomAD_exomes)
                                    HGVS:
                                    NC_000019.10:g.49475734G>A, NC_000019.9:g.49978991G>A, NM_001459.4:c.77G>A, NM_001459.3:c.77G>A, XM_011526676.4:c.77G>A, XM_011526676.3:c.77G>A, XM_011526676.2:c.77G>A, XM_011526676.1:c.77G>A, XM_006723116.4:c.77G>A, XM_006723116.3:c.77G>A, XM_006723116.2:c.77G>A, XM_006723116.1:c.206G>A, XM_011526675.3:c.77G>A, XM_011526675.2:c.77G>A, XM_011526675.1:c.77G>A, XM_011526677.3:c.77G>A, XM_011526677.2:c.77G>A, XM_011526677.1:c.77G>A, XM_011526678.3:c.77G>A, XM_011526678.2:c.77G>A, XM_011526678.1:c.77G>A, XM_011526680.3:c.77G>A, XM_011526680.2:c.77G>A, XM_011526680.1:c.77G>A, NM_001204502.2:c.77G>A, NM_001204502.1:c.77G>A, NM_001278637.2:c.-198G>A, NM_001278637.1:c.-198G>A, NM_001278638.2:c.-170G>A, NM_001278638.1:c.-170G>A, NM_001204503.2:c.77G>A, NM_001204503.1:c.77G>A, XM_047438522.1:c.77G>A, XM_047438519.1:c.77G>A, XM_047438523.1:c.77G>A, XM_047438520.1:c.77G>A, XM_047438521.1:c.77G>A, NP_001450.2:p.Gly26Glu, XP_011524978.1:p.Gly26Glu, XP_006723179.2:p.Gly26Glu, XP_011524977.1:p.Gly26Glu, XP_011524979.1:p.Gly26Glu, XP_011524980.1:p.Gly26Glu, XP_011524982.1:p.Gly26Glu, NP_001191431.1:p.Gly26Glu, NP_001191432.1:p.Gly26Glu, XP_047294478.1:p.Gly26Glu, XP_047294475.1:p.Gly26Glu, XP_047294479.1:p.Gly26Glu, XP_047294476.1:p.Gly26Glu, XP_047294477.1:p.Gly26Glu

                                    18.

                                    rs1412658092 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>A [Show Flanks]
                                      Chromosome:
                                      19:49476506 (GRCh38)
                                      19:49979763 (GRCh37)
                                      Canonical SPDI:
                                      NC_000019.10:49476505:G:A
                                      Gene:
                                      FLT3LG (Varview)
                                      Functional Consequence:
                                      missense_variant,coding_sequence_variant
                                      Validated:
                                      by frequency,by cluster
                                      MAF:
                                      A=0.000004/1 (GnomAD_exomes)
                                      HGVS:
                                      NC_000019.10:g.49476506G>A, NC_000019.9:g.49979763G>A, NM_001459.4:c.282G>A, NM_001459.3:c.282G>A, XM_011526676.4:c.282G>A, XM_011526676.3:c.282G>A, XM_011526676.2:c.282G>A, XM_011526676.1:c.282G>A, XM_006723116.4:c.282G>A, XM_006723116.3:c.282G>A, XM_006723116.2:c.282G>A, XM_006723116.1:c.411G>A, XM_011526675.3:c.282G>A, XM_011526675.2:c.282G>A, XM_011526675.1:c.282G>A, XM_011526677.3:c.282G>A, XM_011526677.2:c.282G>A, XM_011526677.1:c.282G>A, XM_011526678.3:c.282G>A, XM_011526678.2:c.282G>A, XM_011526678.1:c.282G>A, XM_011526680.3:c.282G>A, XM_011526680.2:c.282G>A, XM_011526680.1:c.282G>A, NM_001204502.2:c.282G>A, NM_001204502.1:c.282G>A, NM_001278637.2:c.36G>A, NM_001278637.1:c.36G>A, NM_001278638.2:c.36G>A, NM_001278638.1:c.36G>A, NM_001204503.2:c.282G>A, NM_001204503.1:c.282G>A, XM_047438522.1:c.282G>A, XM_047438519.1:c.282G>A, XM_047438523.1:c.282G>A, XM_047438520.1:c.282G>A, XM_047438521.1:c.282G>A, NP_001450.2:p.Met94Ile, XP_011524978.1:p.Met94Ile, XP_006723179.2:p.Met94Ile, XP_011524977.1:p.Met94Ile, XP_011524979.1:p.Met94Ile, XP_011524980.1:p.Met94Ile, XP_011524982.1:p.Met94Ile, NP_001191431.1:p.Met94Ile, NP_001265566.1:p.Met12Ile, NP_001265567.1:p.Met12Ile, NP_001191432.1:p.Met94Ile, XP_047294478.1:p.Met94Ile, XP_047294475.1:p.Met94Ile, XP_047294479.1:p.Met94Ile, XP_047294476.1:p.Met94Ile, XP_047294477.1:p.Met94Ile

                                      19.

                                      rs1411750444 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        19:49486063 (GRCh38)
                                        19:49989320 (GRCh37)
                                        Canonical SPDI:
                                        NC_000019.10:49486062:T:C
                                        Gene:
                                        FLT3LG (Varview), RPL13A (Varview)
                                        Functional Consequence:
                                        missense_variant,genic_downstream_transcript_variant,stop_lost,coding_sequence_variant,3_prime_UTR_variant,upstream_transcript_variant,terminator_codon_variant,2KB_upstream_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        C=0./0 (ALFA)
                                        C=0.000007/1 (GnomAD)
                                        C=0.000008/2 (TOPMED)
                                        HGVS:
                                        NC_000019.10:g.49486063T>C, NC_000019.9:g.49989320T>C, NM_001459.4:c.*70T>C, NM_001459.3:c.*70T>C, XM_011526676.4:c.599T>C, XM_011526676.3:c.599T>C, XM_011526676.2:c.599T>C, XM_011526676.1:c.599T>C, XM_011526675.3:c.599T>C, XM_011526675.2:c.599T>C, XM_011526675.1:c.599T>C, XM_011526677.3:c.*89T>C, XM_011526678.3:c.545T>C, XM_011526678.2:c.545T>C, XM_011526678.1:c.545T>C, XM_011526680.3:c.391T>C, XM_011526680.2:c.391T>C, XM_011526680.1:c.391T>C, NM_001204502.2:c.*121T>C, NM_001204502.1:c.*121T>C, NM_001278637.2:c.*70T>C, NM_001278637.1:c.*70T>C, NM_001278638.2:c.*70T>C, NM_001278638.1:c.*70T>C, NM_001204503.2:c.*121T>C, NM_001204503.1:c.*121T>C, XM_047438522.1:c.*36T>C, XM_047438519.1:c.709T>C, XM_047438523.1:c.*36T>C, XM_047438521.1:c.*36T>C, XP_011524978.1:p.Ile200Thr, XP_011524977.1:p.Ile200Thr, XP_011524980.1:p.Ile182Thr, XP_011524982.1:p.Ter131Gln, XP_047294475.1:p.Ter237Gln

                                        20.

                                        rs1390494607 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          19:49480590 (GRCh38)
                                          19:49983847 (GRCh37)
                                          Canonical SPDI:
                                          NC_000019.10:49480589:G:A
                                          Gene:
                                          FLT3LG (Varview)
                                          Functional Consequence:
                                          intron_variant,coding_sequence_variant,stop_gained,synonymous_variant,missense_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.49480590G>A, NC_000019.9:g.49983847G>A, NM_001459.4:c.699G>A, NM_001459.3:c.699G>A, XM_011526676.4:c.520G>A, XM_011526676.3:c.520G>A, XM_011526676.2:c.520G>A, XM_011526676.1:c.520G>A, XM_006723116.4:c.560G>A, XM_006723116.3:c.560G>A, XM_006723116.2:c.560G>A, XM_006723116.1:c.689G>A, XM_011526675.3:c.520G>A, XM_011526675.2:c.520G>A, XM_011526675.1:c.520G>A, XM_011526677.3:c.520G>A, XM_011526677.2:c.520G>A, XM_011526677.1:c.520G>A, XM_011526678.3:c.466G>A, XM_011526678.2:c.466G>A, XM_011526678.1:c.466G>A, NM_001204502.2:c.699G>A, NM_001204502.1:c.699G>A, NM_001278637.2:c.453G>A, NM_001278637.1:c.453G>A, NM_001278638.2:c.453G>A, NM_001278638.1:c.453G>A, NM_001204503.2:c.699G>A, NM_001204503.1:c.699G>A, XM_047438522.1:c.560G>A, XM_047438523.1:c.560G>A, XM_047438520.1:c.699G>A, XP_011524978.1:p.Gly174Arg, XP_006723179.2:p.Trp187Ter, XP_011524977.1:p.Gly174Arg, XP_011524979.1:p.Gly174Arg, XP_011524980.1:p.Gly156Arg, XP_047294478.1:p.Trp187Ter, XP_047294479.1:p.Trp187Ter

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