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Items: 1 to 20 of 1000

1.

rs1490764844 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    6:32444898 (GRCh38)
    6:32412675 (GRCh37)
    Canonical SPDI:
    NC_000006.12:32444897:C:T
    Gene:
    HLA-DRA (Varview)
    Functional Consequence:
    3_prime_UTR_variant
    Validated:
    by frequency,by alfa
    MAF:
    T=0./0 (ALFA)
    T=0.000004/1 (TOPMED)
    HGVS:

    2.

    rs1490605350 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>G [Show Flanks]
      Chromosome:
      6:32445423 (GRCh38)
      6:32413200 (GRCh37)
      Canonical SPDI:
      NC_000006.12:32445422:A:G
      Gene:
      HLA-DRA (Varview)
      Functional Consequence:
      downstream_transcript_variant,500B_downstream_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      G=0./0 (ALFA)
      G=0.000021/3 (GnomAD)
      G=0.000026/7 (TOPMED)
      HGVS:

      3.

      rs1490390267 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>T [Show Flanks]
        Chromosome:
        6:32444265 (GRCh38)
        6:32412042 (GRCh37)
        Canonical SPDI:
        NC_000006.12:32444264:C:T
        Gene:
        HLA-DRA (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        T=0./0 (ALFA)
        T=0.000004/1 (TOPMED)
        HGVS:

        4.

        rs1490075436 [Homo sapiens]
          Variant type:
          DEL
          Alleles:
          T>- [Show Flanks]
          Chromosome:
          6:32444454 (GRCh38)
          6:32412231 (GRCh37)
          Canonical SPDI:
          NC_000006.12:32444453:T:
          Gene:
          HLA-DRA (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          -=0./0 (ALFA)
          -=0.000004/1 (TOPMED)
          -=0.000007/1 (GnomAD)
          HGVS:

          5.

          rs1489530240 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>C [Show Flanks]
            Chromosome:
            6:32442028 (GRCh38)
            6:32409805 (GRCh37)
            Canonical SPDI:
            NC_000006.12:32442027:T:C
            Gene:
            HLA-DRA (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            C=0.000132/2 (ALFA)
            C=0.000004/1 (TOPMED)
            C=0.000007/1 (GnomAD)
            C=0.000035/1 (TOMMO)
            C=0.000446/2 (Estonian)
            HGVS:

            6.

            rs1489279106 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>C [Show Flanks]
              Chromosome:
              6:32441189 (GRCh38)
              6:32408966 (GRCh37)
              Canonical SPDI:
              NC_000006.12:32441188:T:C
              Gene:
              HLA-DRA (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa
              MAF:
              C=0./0 (ALFA)
              C=0.000004/1 (TOPMED)
              HGVS:

              7.

              rs1488488954 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>A,C [Show Flanks]
                Chromosome:
                6:32442911 (GRCh38)
                6:32410688 (GRCh37)
                Canonical SPDI:
                NC_000006.12:32442910:T:A,NC_000006.12:32442910:T:C
                Gene:
                HLA-DRA (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                C=0./0 (ALFA)
                HGVS:
                NC_000006.12:g.32442911T>A, NC_000006.12:g.32442911T>C, NC_000006.11:g.32410688T>A, NC_000006.11:g.32410688T>C, NT_113891.3:g.3881034T>A, NT_113891.3:g.3881034T>C, NT_113891.2:g.3881140T>A, NT_113891.2:g.3881140T>C, NG_002392.2:g.7245T>A, NG_002392.2:g.7245T>C, NT_167248.2:g.3665958T>A, NT_167248.2:g.3665958T>C, NT_167248.1:g.3671554T>A, NT_167248.1:g.3671554T>C, NT_167245.2:g.3683214T>A, NT_167245.2:g.3683214T>C, NT_167245.1:g.3688799T>A, NT_167245.1:g.3688799T>C, NT_167249.2:g.3758052T>A, NT_167249.2:g.3758052T>C, NT_167249.1:g.3757350T>A, NT_167249.1:g.3757350T>C, NT_167246.2:g.3747127T>A, NT_167246.2:g.3747127T>C, NT_167246.1:g.3752747T>A, NT_167246.1:g.3752747T>C, NT_167247.2:g.3783875T>A, NT_167247.2:g.3783875T>C, NT_167247.1:g.3789460T>A, NT_167247.1:g.3789460T>C, NT_187692.1:g.11822A>T, NT_187692.1:g.11822A>G

                8.

                rs1487083378 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>C [Show Flanks]
                  Chromosome:
                  6:32440104 (GRCh38)
                  6:32407881 (GRCh37)
                  Canonical SPDI:
                  NC_000006.12:32440103:G:C
                  Gene:
                  HLA-DRA (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  C=0.000071/1 (ALFA)
                  C=0.000004/1 (TOPMED)
                  C=0.000007/1 (GnomAD)
                  HGVS:

                  9.

                  rs1487058075 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A [Show Flanks]
                    Chromosome:
                    6:32441782 (GRCh38)
                    6:32409559 (GRCh37)
                    Canonical SPDI:
                    NC_000006.12:32441781:G:A
                    Gene:
                    HLA-DRA (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    A=0./0 (ALFA)
                    A=0.000004/1 (TOPMED)
                    A=0.000007/1 (GnomAD)
                    HGVS:

                    10.

                    rs1487053035 has merged into rs28993482 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      AAAAAAAAAAAAAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                      Chromosome:
                      6:32439080 (GRCh38)
                      6:32406857 (GRCh37)
                      Canonical SPDI:
                      NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32439070:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                      Gene:
                      HLA-DRA (Varview)
                      Functional Consequence:
                      2KB_upstream_variant,upstream_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      AAAAAAAAA=0./0 (ALFA)
                      HGVS:
                      NC_000006.12:g.32439080_32439093del, NC_000006.12:g.32439081_32439093del, NC_000006.12:g.32439082_32439093del, NC_000006.12:g.32439084_32439093del, NC_000006.12:g.32439085_32439093del, NC_000006.12:g.32439086_32439093del, NC_000006.12:g.32439088_32439093del, NC_000006.12:g.32439089_32439093del, NC_000006.12:g.32439090_32439093del, NC_000006.12:g.32439091_32439093del, NC_000006.12:g.32439092_32439093del, NC_000006.12:g.32439093del, NC_000006.12:g.32439093dup, NC_000006.12:g.32439092_32439093dup, NC_000006.12:g.32439091_32439093dup, NC_000006.12:g.32439090_32439093dup, NC_000006.12:g.32439089_32439093dup, NC_000006.12:g.32439088_32439093dup, NC_000006.12:g.32439087_32439093dup, NC_000006.12:g.32439086_32439093dup, NC_000006.12:g.32439085_32439093dup, NC_000006.12:g.32439084_32439093dup, NC_000006.12:g.32439083_32439093dup, NC_000006.12:g.32439082_32439093dup, NC_000006.12:g.32439081_32439093dup, NC_000006.12:g.32439080_32439093dup, NC_000006.12:g.32439079_32439093dup, NC_000006.12:g.32439078_32439093dup, NC_000006.12:g.32439077_32439093dup, NC_000006.12:g.32439076_32439093dup, NC_000006.12:g.32439075_32439093dup, NC_000006.12:g.32439074_32439093dup, NC_000006.12:g.32439073_32439093dup, NC_000006.12:g.32439072_32439093dup, NC_000006.12:g.32439071_32439093dup, NC_000006.12:g.32439093_32439094insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32439093_32439094insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32439093_32439094insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32439093_32439094insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32406857_32406870del, NC_000006.11:g.32406858_32406870del, NC_000006.11:g.32406859_32406870del, NC_000006.11:g.32406861_32406870del, NC_000006.11:g.32406862_32406870del, NC_000006.11:g.32406863_32406870del, NC_000006.11:g.32406865_32406870del, NC_000006.11:g.32406866_32406870del, NC_000006.11:g.32406867_32406870del, NC_000006.11:g.32406868_32406870del, NC_000006.11:g.32406869_32406870del, NC_000006.11:g.32406870del, NC_000006.11:g.32406870dup, NC_000006.11:g.32406869_32406870dup, NC_000006.11:g.32406868_32406870dup, NC_000006.11:g.32406867_32406870dup, NC_000006.11:g.32406866_32406870dup, NC_000006.11:g.32406865_32406870dup, NC_000006.11:g.32406864_32406870dup, NC_000006.11:g.32406863_32406870dup, NC_000006.11:g.32406862_32406870dup, NC_000006.11:g.32406861_32406870dup, NC_000006.11:g.32406860_32406870dup, NC_000006.11:g.32406859_32406870dup, NC_000006.11:g.32406858_32406870dup, NC_000006.11:g.32406857_32406870dup, NC_000006.11:g.32406856_32406870dup, NC_000006.11:g.32406855_32406870dup, NC_000006.11:g.32406854_32406870dup, NC_000006.11:g.32406853_32406870dup, NC_000006.11:g.32406852_32406870dup, NC_000006.11:g.32406851_32406870dup, NC_000006.11:g.32406850_32406870dup, NC_000006.11:g.32406849_32406870dup, NC_000006.11:g.32406848_32406870dup, NC_000006.11:g.32406870_32406871insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32406870_32406871insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32406870_32406871insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32406870_32406871insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3877209_3877222del, NT_113891.3:g.3877210_3877222del, NT_113891.3:g.3877211_3877222del, NT_113891.3:g.3877213_3877222del, NT_113891.3:g.3877214_3877222del, NT_113891.3:g.3877215_3877222del, NT_113891.3:g.3877217_3877222del, NT_113891.3:g.3877218_3877222del, NT_113891.3:g.3877219_3877222del, NT_113891.3:g.3877220_3877222del, NT_113891.3:g.3877221_3877222del, NT_113891.3:g.3877222del, NT_113891.3:g.3877222dup, NT_113891.3:g.3877221_3877222dup, NT_113891.3:g.3877220_3877222dup, NT_113891.3:g.3877219_3877222dup, NT_113891.3:g.3877218_3877222dup, NT_113891.3:g.3877217_3877222dup, NT_113891.3:g.3877216_3877222dup, NT_113891.3:g.3877215_3877222dup, NT_113891.3:g.3877214_3877222dup, NT_113891.3:g.3877213_3877222dup, NT_113891.3:g.3877212_3877222dup, NT_113891.3:g.3877211_3877222dup, NT_113891.3:g.3877210_3877222dup, NT_113891.3:g.3877209_3877222dup, NT_113891.3:g.3877208_3877222dup, NT_113891.3:g.3877207_3877222dup, NT_113891.3:g.3877206_3877222dup, NT_113891.3:g.3877205_3877222dup, NT_113891.3:g.3877204_3877222dup, NT_113891.3:g.3877203_3877222dup, NT_113891.3:g.3877202_3877222dup, NT_113891.3:g.3877201_3877222dup, NT_113891.3:g.3877200_3877222dup, NT_113891.3:g.3877199_3877222dup, NT_113891.3:g.3877198_3877222dup, NT_113891.3:g.3877196_3877222dup, NT_113891.3:g.3877195_3877222dup, NT_113891.2:g.3877315_3877328del, NT_113891.2:g.3877316_3877328del, NT_113891.2:g.3877317_3877328del, NT_113891.2:g.3877319_3877328del, NT_113891.2:g.3877320_3877328del, NT_113891.2:g.3877321_3877328del, NT_113891.2:g.3877323_3877328del, NT_113891.2:g.3877324_3877328del, NT_113891.2:g.3877325_3877328del, NT_113891.2:g.3877326_3877328del, NT_113891.2:g.3877327_3877328del, NT_113891.2:g.3877328del, NT_113891.2:g.3877328dup, NT_113891.2:g.3877327_3877328dup, NT_113891.2:g.3877326_3877328dup, NT_113891.2:g.3877325_3877328dup, NT_113891.2:g.3877324_3877328dup, NT_113891.2:g.3877323_3877328dup, NT_113891.2:g.3877322_3877328dup, NT_113891.2:g.3877321_3877328dup, NT_113891.2:g.3877320_3877328dup, NT_113891.2:g.3877319_3877328dup, NT_113891.2:g.3877318_3877328dup, NT_113891.2:g.3877317_3877328dup, NT_113891.2:g.3877316_3877328dup, NT_113891.2:g.3877315_3877328dup, NT_113891.2:g.3877314_3877328dup, NT_113891.2:g.3877313_3877328dup, NT_113891.2:g.3877312_3877328dup, NT_113891.2:g.3877311_3877328dup, NT_113891.2:g.3877310_3877328dup, NT_113891.2:g.3877309_3877328dup, NT_113891.2:g.3877308_3877328dup, NT_113891.2:g.3877307_3877328dup, NT_113891.2:g.3877306_3877328dup, NT_113891.2:g.3877305_3877328dup, NT_113891.2:g.3877304_3877328dup, NT_113891.2:g.3877302_3877328dup, NT_113891.2:g.3877301_3877328dup, NG_002392.2:g.3420_3433del, NG_002392.2:g.3421_3433del, NG_002392.2:g.3422_3433del, NG_002392.2:g.3424_3433del, NG_002392.2:g.3425_3433del, NG_002392.2:g.3426_3433del, NG_002392.2:g.3428_3433del, NG_002392.2:g.3429_3433del, NG_002392.2:g.3430_3433del, NG_002392.2:g.3431_3433del, NG_002392.2:g.3432_3433del, NG_002392.2:g.3433del, NG_002392.2:g.3433dup, NG_002392.2:g.3432_3433dup, NG_002392.2:g.3431_3433dup, NG_002392.2:g.3430_3433dup, NG_002392.2:g.3429_3433dup, NG_002392.2:g.3428_3433dup, NG_002392.2:g.3427_3433dup, NG_002392.2:g.3426_3433dup, NG_002392.2:g.3425_3433dup, NG_002392.2:g.3424_3433dup, NG_002392.2:g.3423_3433dup, NG_002392.2:g.3422_3433dup, NG_002392.2:g.3421_3433dup, NG_002392.2:g.3420_3433dup, NG_002392.2:g.3419_3433dup, NG_002392.2:g.3418_3433dup, NG_002392.2:g.3417_3433dup, NG_002392.2:g.3416_3433dup, NG_002392.2:g.3415_3433dup, NG_002392.2:g.3414_3433dup, NG_002392.2:g.3413_3433dup, NG_002392.2:g.3412_3433dup, NG_002392.2:g.3411_3433dup, NG_002392.2:g.3410_3433dup, NG_002392.2:g.3409_3433dup, NG_002392.2:g.3407_3433dup, NG_002392.2:g.3406_3433dup, NT_167248.2:g.3662142dup, NT_167248.2:g.3662130_3662142del, NT_167248.2:g.3662131_3662142del, NT_167248.2:g.3662132_3662142del, NT_167248.2:g.3662134_3662142del, NT_167248.2:g.3662135_3662142del, NT_167248.2:g.3662136_3662142del, NT_167248.2:g.3662138_3662142del, NT_167248.2:g.3662139_3662142del, NT_167248.2:g.3662140_3662142del, NT_167248.2:g.3662141_3662142del, NT_167248.2:g.3662142del, NT_167248.2:g.3662141_3662142dup, NT_167248.2:g.3662140_3662142dup, NT_167248.2:g.3662139_3662142dup, NT_167248.2:g.3662138_3662142dup, NT_167248.2:g.3662137_3662142dup, NT_167248.2:g.3662136_3662142dup, NT_167248.2:g.3662135_3662142dup, NT_167248.2:g.3662134_3662142dup, NT_167248.2:g.3662133_3662142dup, NT_167248.2:g.3662132_3662142dup, NT_167248.2:g.3662131_3662142dup, NT_167248.2:g.3662130_3662142dup, NT_167248.2:g.3662129_3662142dup, NT_167248.2:g.3662128_3662142dup, NT_167248.2:g.3662127_3662142dup, NT_167248.2:g.3662126_3662142dup, NT_167248.2:g.3662125_3662142dup, NT_167248.2:g.3662124_3662142dup, NT_167248.2:g.3662123_3662142dup, NT_167248.2:g.3662122_3662142dup, NT_167248.2:g.3662121_3662142dup, NT_167248.2:g.3662142_3662143insAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3662142_3662143insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3662142_3662143insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3662142_3662143insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3662142_3662143insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3662142_3662143insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3679397_3679398dup, NT_167245.2:g.3679387_3679398del, NT_167245.2:g.3679388_3679398del, NT_167245.2:g.3679389_3679398del, NT_167245.2:g.3679391_3679398del, NT_167245.2:g.3679392_3679398del, NT_167245.2:g.3679393_3679398del, NT_167245.2:g.3679395_3679398del, NT_167245.2:g.3679396_3679398del, NT_167245.2:g.3679397_3679398del, NT_167245.2:g.3679398del, NT_167245.2:g.3679398dup, NT_167245.2:g.3679396_3679398dup, NT_167245.2:g.3679395_3679398dup, NT_167245.2:g.3679394_3679398dup, NT_167245.2:g.3679393_3679398dup, NT_167245.2:g.3679392_3679398dup, NT_167245.2:g.3679391_3679398dup, NT_167245.2:g.3679390_3679398dup, NT_167245.2:g.3679389_3679398dup, NT_167245.2:g.3679388_3679398dup, NT_167245.2:g.3679387_3679398dup, NT_167245.2:g.3679386_3679398dup, NT_167245.2:g.3679385_3679398dup, NT_167245.2:g.3679384_3679398dup, NT_167245.2:g.3679383_3679398dup, NT_167245.2:g.3679382_3679398dup, NT_167245.2:g.3679381_3679398dup, NT_167245.2:g.3679380_3679398dup, NT_167245.2:g.3679379_3679398dup, NT_167245.2:g.3679378_3679398dup, NT_167245.2:g.3679398_3679399insAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3679398_3679399insAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3679398_3679399insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3679398_3679399insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3679398_3679399insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3679398_3679399insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3679398_3679399insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3679398_3679399insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3754234_3754236dup, NT_167249.2:g.3754226_3754236del, NT_167249.2:g.3754227_3754236del, NT_167249.2:g.3754228_3754236del, NT_167249.2:g.3754230_3754236del, NT_167249.2:g.3754231_3754236del, NT_167249.2:g.3754232_3754236del, NT_167249.2:g.3754234_3754236del, NT_167249.2:g.3754235_3754236del, NT_167249.2:g.3754236del, NT_167249.2:g.3754236dup, NT_167249.2:g.3754235_3754236dup, NT_167249.2:g.3754233_3754236dup, NT_167249.2:g.3754232_3754236dup, NT_167249.2:g.3754231_3754236dup, NT_167249.2:g.3754230_3754236dup, NT_167249.2:g.3754229_3754236dup, NT_167249.2:g.3754228_3754236dup, NT_167249.2:g.3754227_3754236dup, NT_167249.2:g.3754226_3754236dup, NT_167249.2:g.3754225_3754236dup, NT_167249.2:g.3754224_3754236dup, NT_167249.2:g.3754223_3754236dup, NT_167249.2:g.3754222_3754236dup, NT_167249.2:g.3754221_3754236dup, NT_167249.2:g.3754220_3754236dup, NT_167249.2:g.3754219_3754236dup, NT_167249.2:g.3754218_3754236dup, NT_167249.2:g.3754217_3754236dup, NT_167249.2:g.3754236_3754237insAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3754236_3754237insAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3754236_3754237insAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3754236_3754237insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3754236_3754237insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3754236_3754237insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3754236_3754237insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3754236_3754237insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3754236_3754237insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3754236_3754237insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3743310dup, NT_167246.2:g.3743298_3743310del, NT_167246.2:g.3743299_3743310del, NT_167246.2:g.3743300_3743310del, NT_167246.2:g.3743302_3743310del, NT_167246.2:g.3743303_3743310del, NT_167246.2:g.3743304_3743310del, NT_167246.2:g.3743306_3743310del, NT_167246.2:g.3743307_3743310del, NT_167246.2:g.3743308_3743310del, NT_167246.2:g.3743309_3743310del, NT_167246.2:g.3743310del, NT_167246.2:g.3743309_3743310dup, NT_167246.2:g.3743308_3743310dup, NT_167246.2:g.3743307_3743310dup, NT_167246.2:g.3743306_3743310dup, NT_167246.2:g.3743305_3743310dup, NT_167246.2:g.3743304_3743310dup, NT_167246.2:g.3743303_3743310dup, NT_167246.2:g.3743302_3743310dup, NT_167246.2:g.3743301_3743310dup, NT_167246.2:g.3743300_3743310dup, NT_167246.2:g.3743299_3743310dup, NT_167246.2:g.3743298_3743310dup, NT_167246.2:g.3743297_3743310dup, NT_167246.2:g.3743296_3743310dup, NT_167246.2:g.3743295_3743310dup, NT_167246.2:g.3743294_3743310dup, NT_167246.2:g.3743293_3743310dup, NT_167246.2:g.3743292_3743310dup, NT_167246.2:g.3743291_3743310dup, NT_167246.2:g.3743290_3743310dup, NT_167246.2:g.3743289_3743310dup, NT_167246.2:g.3743310_3743311insAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3743310_3743311insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3743310_3743311insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3743310_3743311insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3743310_3743311insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3743310_3743311insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3780057_3780059dup, NT_167247.2:g.3780049_3780059del, NT_167247.2:g.3780050_3780059del, NT_167247.2:g.3780051_3780059del, NT_167247.2:g.3780053_3780059del, NT_167247.2:g.3780054_3780059del, NT_167247.2:g.3780055_3780059del, NT_167247.2:g.3780057_3780059del, NT_167247.2:g.3780058_3780059del, NT_167247.2:g.3780059del, NT_167247.2:g.3780059dup, NT_167247.2:g.3780058_3780059dup, NT_167247.2:g.3780056_3780059dup, NT_167247.2:g.3780055_3780059dup, NT_167247.2:g.3780054_3780059dup, NT_167247.2:g.3780053_3780059dup, NT_167247.2:g.3780052_3780059dup, NT_167247.2:g.3780051_3780059dup, NT_167247.2:g.3780050_3780059dup, NT_167247.2:g.3780049_3780059dup, NT_167247.2:g.3780048_3780059dup, NT_167247.2:g.3780047_3780059dup, NT_167247.2:g.3780046_3780059dup, NT_167247.2:g.3780045_3780059dup, NT_167247.2:g.3780044_3780059dup, NT_167247.2:g.3780043_3780059dup, NT_167247.2:g.3780042_3780059dup, NT_167247.2:g.3780041_3780059dup, NT_167247.2:g.3780040_3780059dup, NT_167247.2:g.3780059_3780060insAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3780059_3780060insAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3780059_3780060insAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3780059_3780060insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3780059_3780060insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3780059_3780060insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3780059_3780060insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3780059_3780060insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3780059_3780060insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3780059_3780060insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187692.1:g.15649_15662del, NT_187692.1:g.15650_15662del, NT_187692.1:g.15651_15662del, NT_187692.1:g.15653_15662del, NT_187692.1:g.15654_15662del, NT_187692.1:g.15655_15662del, NT_187692.1:g.15657_15662del, NT_187692.1:g.15658_15662del, NT_187692.1:g.15659_15662del, NT_187692.1:g.15660_15662del, NT_187692.1:g.15661_15662del, NT_187692.1:g.15662del, NT_187692.1:g.15662dup, NT_187692.1:g.15661_15662dup, NT_187692.1:g.15660_15662dup, NT_187692.1:g.15659_15662dup, NT_187692.1:g.15658_15662dup, NT_187692.1:g.15657_15662dup, NT_187692.1:g.15656_15662dup, NT_187692.1:g.15655_15662dup, NT_187692.1:g.15654_15662dup, NT_187692.1:g.15653_15662dup, NT_187692.1:g.15652_15662dup, NT_187692.1:g.15651_15662dup, NT_187692.1:g.15650_15662dup, NT_187692.1:g.15649_15662dup, NT_187692.1:g.15648_15662dup, NT_187692.1:g.15647_15662dup, NT_187692.1:g.15646_15662dup, NT_187692.1:g.15645_15662dup, NT_187692.1:g.15644_15662dup, NT_187692.1:g.15643_15662dup, NT_187692.1:g.15642_15662dup, NT_187692.1:g.15641_15662dup, NT_187692.1:g.15640_15662dup, NT_187692.1:g.15662_15663insTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.15662_15663insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.15662_15663insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.15662_15663insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.3667738dup, NT_167248.1:g.3667726_3667738del, NT_167248.1:g.3667727_3667738del, NT_167248.1:g.3667728_3667738del, NT_167248.1:g.3667730_3667738del, NT_167248.1:g.3667731_3667738del, NT_167248.1:g.3667732_3667738del, NT_167248.1:g.3667734_3667738del, NT_167248.1:g.3667735_3667738del, NT_167248.1:g.3667736_3667738del, NT_167248.1:g.3667737_3667738del, NT_167248.1:g.3667738del, NT_167248.1:g.3667737_3667738dup, NT_167248.1:g.3667736_3667738dup, NT_167248.1:g.3667735_3667738dup, NT_167248.1:g.3667734_3667738dup, NT_167248.1:g.3667733_3667738dup, NT_167248.1:g.3667732_3667738dup, NT_167248.1:g.3667731_3667738dup, NT_167248.1:g.3667730_3667738dup, NT_167248.1:g.3667729_3667738dup, NT_167248.1:g.3667728_3667738dup, NT_167248.1:g.3667727_3667738dup, NT_167248.1:g.3667726_3667738dup, NT_167248.1:g.3667725_3667738dup, NT_167248.1:g.3667724_3667738dup, NT_167248.1:g.3667723_3667738dup, NT_167248.1:g.3667722_3667738dup, NT_167248.1:g.3667721_3667738dup, NT_167248.1:g.3667720_3667738dup, NT_167248.1:g.3667719_3667738dup, NT_167248.1:g.3667718_3667738dup, NT_167248.1:g.3667717_3667738dup, NT_167248.1:g.3667738_3667739insAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3667738_3667739insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3667738_3667739insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3667738_3667739insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3667738_3667739insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3667738_3667739insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3684982_3684983dup, NT_167245.1:g.3684972_3684983del, NT_167245.1:g.3684973_3684983del, NT_167245.1:g.3684974_3684983del, NT_167245.1:g.3684976_3684983del, NT_167245.1:g.3684977_3684983del, NT_167245.1:g.3684978_3684983del, NT_167245.1:g.3684980_3684983del, NT_167245.1:g.3684981_3684983del, NT_167245.1:g.3684982_3684983del, NT_167245.1:g.3684983del, NT_167245.1:g.3684983dup, NT_167245.1:g.3684981_3684983dup, NT_167245.1:g.3684980_3684983dup, NT_167245.1:g.3684979_3684983dup, NT_167245.1:g.3684978_3684983dup, NT_167245.1:g.3684977_3684983dup, NT_167245.1:g.3684976_3684983dup, NT_167245.1:g.3684975_3684983dup, NT_167245.1:g.3684974_3684983dup, NT_167245.1:g.3684973_3684983dup, NT_167245.1:g.3684972_3684983dup, NT_167245.1:g.3684971_3684983dup, NT_167245.1:g.3684970_3684983dup, NT_167245.1:g.3684969_3684983dup, NT_167245.1:g.3684968_3684983dup, NT_167245.1:g.3684967_3684983dup, NT_167245.1:g.3684966_3684983dup, NT_167245.1:g.3684965_3684983dup, NT_167245.1:g.3684964_3684983dup, NT_167245.1:g.3684963_3684983dup, NT_167245.1:g.3684983_3684984insAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3684983_3684984insAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3684983_3684984insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3684983_3684984insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3684983_3684984insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3684983_3684984insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3684983_3684984insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3684983_3684984insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3753532_3753534dup, NT_167249.1:g.3753524_3753534del, NT_167249.1:g.3753525_3753534del, NT_167249.1:g.3753526_3753534del, NT_167249.1:g.3753528_3753534del, NT_167249.1:g.3753529_3753534del, NT_167249.1:g.3753530_3753534del, NT_167249.1:g.3753532_3753534del, NT_167249.1:g.3753533_3753534del, NT_167249.1:g.3753534del, NT_167249.1:g.3753534dup, NT_167249.1:g.3753533_3753534dup, NT_167249.1:g.3753531_3753534dup, NT_167249.1:g.3753530_3753534dup, NT_167249.1:g.3753529_3753534dup, NT_167249.1:g.3753528_3753534dup, NT_167249.1:g.3753527_3753534dup, NT_167249.1:g.3753526_3753534dup, NT_167249.1:g.3753525_3753534dup, NT_167249.1:g.3753524_3753534dup, NT_167249.1:g.3753523_3753534dup, NT_167249.1:g.3753522_3753534dup, NT_167249.1:g.3753521_3753534dup, NT_167249.1:g.3753520_3753534dup, NT_167249.1:g.3753519_3753534dup, NT_167249.1:g.3753518_3753534dup, NT_167249.1:g.3753517_3753534dup, NT_167249.1:g.3753516_3753534dup, NT_167249.1:g.3753515_3753534dup, NT_167249.1:g.3753534_3753535insAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3753534_3753535insAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3753534_3753535insAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3753534_3753535insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3753534_3753535insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3753534_3753535insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3753534_3753535insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3753534_3753535insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3753534_3753535insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3753534_3753535insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3748930dup, NT_167246.1:g.3748918_3748930del, NT_167246.1:g.3748919_3748930del, NT_167246.1:g.3748920_3748930del, NT_167246.1:g.3748922_3748930del, NT_167246.1:g.3748923_3748930del, NT_167246.1:g.3748924_3748930del, NT_167246.1:g.3748926_3748930del, NT_167246.1:g.3748927_3748930del, NT_167246.1:g.3748928_3748930del, NT_167246.1:g.3748929_3748930del, NT_167246.1:g.3748930del, NT_167246.1:g.3748929_3748930dup, NT_167246.1:g.3748928_3748930dup, NT_167246.1:g.3748927_3748930dup, NT_167246.1:g.3748926_3748930dup, NT_167246.1:g.3748925_3748930dup, NT_167246.1:g.3748924_3748930dup, NT_167246.1:g.3748923_3748930dup, NT_167246.1:g.3748922_3748930dup, NT_167246.1:g.3748921_3748930dup, NT_167246.1:g.3748920_3748930dup, NT_167246.1:g.3748919_3748930dup, NT_167246.1:g.3748918_3748930dup, NT_167246.1:g.3748917_3748930dup, NT_167246.1:g.3748916_3748930dup, NT_167246.1:g.3748915_3748930dup, NT_167246.1:g.3748914_3748930dup, NT_167246.1:g.3748913_3748930dup, NT_167246.1:g.3748912_3748930dup, NT_167246.1:g.3748911_3748930dup, NT_167246.1:g.3748910_3748930dup, NT_167246.1:g.3748909_3748930dup, NT_167246.1:g.3748930_3748931insAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3748930_3748931insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3748930_3748931insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3748930_3748931insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3748930_3748931insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3748930_3748931insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3785642_3785644dup, NT_167247.1:g.3785634_3785644del, NT_167247.1:g.3785635_3785644del, NT_167247.1:g.3785636_3785644del, NT_167247.1:g.3785638_3785644del, NT_167247.1:g.3785639_3785644del, NT_167247.1:g.3785640_3785644del, NT_167247.1:g.3785642_3785644del, NT_167247.1:g.3785643_3785644del, NT_167247.1:g.3785644del, NT_167247.1:g.3785644dup, NT_167247.1:g.3785643_3785644dup, NT_167247.1:g.3785641_3785644dup, NT_167247.1:g.3785640_3785644dup, NT_167247.1:g.3785639_3785644dup, NT_167247.1:g.3785638_3785644dup, NT_167247.1:g.3785637_3785644dup, NT_167247.1:g.3785636_3785644dup, NT_167247.1:g.3785635_3785644dup, NT_167247.1:g.3785634_3785644dup, NT_167247.1:g.3785633_3785644dup, NT_167247.1:g.3785632_3785644dup, NT_167247.1:g.3785631_3785644dup, NT_167247.1:g.3785630_3785644dup, NT_167247.1:g.3785629_3785644dup, NT_167247.1:g.3785628_3785644dup, NT_167247.1:g.3785627_3785644dup, NT_167247.1:g.3785626_3785644dup, NT_167247.1:g.3785625_3785644dup, NT_167247.1:g.3785644_3785645insAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3785644_3785645insAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3785644_3785645insAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3785644_3785645insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3785644_3785645insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3785644_3785645insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3785644_3785645insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3785644_3785645insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3785644_3785645insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3785644_3785645insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

                      11.

                      rs1486986991 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        A>G [Show Flanks]
                        Chromosome:
                        6:32440730 (GRCh38)
                        6:32408507 (GRCh37)
                        Canonical SPDI:
                        NC_000006.12:32440729:A:G
                        Gene:
                        HLA-DRA (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        G=0./0 (ALFA)
                        G=0.000007/1 (GnomAD)
                        G=0.000008/2 (TOPMED)
                        HGVS:

                        12.

                        rs1486234672 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>A,T [Show Flanks]
                          Chromosome:
                          6:32442486 (GRCh38)
                          6:32410263 (GRCh37)
                          Canonical SPDI:
                          NC_000006.12:32442485:C:A,NC_000006.12:32442485:C:T
                          Gene:
                          HLA-DRA (Varview)
                          Functional Consequence:
                          coding_sequence_variant,missense_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          T=0./0 (ALFA)
                          A=0.000004/1 (GnomAD_exomes)
                          HGVS:
                          NC_000006.12:g.32442486C>A, NC_000006.12:g.32442486C>T, NC_000006.11:g.32410263C>A, NC_000006.11:g.32410263C>T, NT_113891.3:g.3880609C>A, NT_113891.3:g.3880609C>T, NT_113891.2:g.3880715C>A, NT_113891.2:g.3880715C>T, NG_002392.2:g.6820C>A, NG_002392.2:g.6820C>T, NT_167248.2:g.3665533C>A, NT_167248.2:g.3665533C>T, NT_167248.1:g.3671129C>A, NT_167248.1:g.3671129C>T, NT_167245.2:g.3682789C>A, NT_167245.2:g.3682789C>T, NT_167245.1:g.3688374C>A, NT_167245.1:g.3688374C>T, NT_167249.2:g.3757627C>A, NT_167249.2:g.3757627C>T, NT_167249.1:g.3756925C>A, NT_167249.1:g.3756925C>T, NT_167246.2:g.3746702C>A, NT_167246.2:g.3746702C>T, NT_167246.1:g.3752322C>A, NT_167246.1:g.3752322C>T, NT_167247.2:g.3783450C>A, NT_167247.2:g.3783450C>T, NT_167247.1:g.3789035C>A, NT_167247.1:g.3789035C>T, NT_187692.1:g.12247G>T, NT_187692.1:g.12247G>A, NM_019111.5:c.121C>A, NM_019111.5:c.121C>T, NM_019111.4:c.121C>A, NM_019111.4:c.121C>T, NP_061984.2:p.Pro41Thr, NP_061984.2:p.Pro41Ser

                          13.

                          rs1486192528 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>A [Show Flanks]
                            Chromosome:
                            6:32440824 (GRCh38)
                            6:32408601 (GRCh37)
                            Canonical SPDI:
                            NC_000006.12:32440823:C:A
                            Gene:
                            HLA-DRA (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            A=0./0 (ALFA)
                            A=0.000004/1 (TOPMED)
                            A=0.000007/1 (GnomAD)
                            HGVS:

                            14.

                            rs1485603097 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C [Show Flanks]
                              Chromosome:
                              6:32438394 (GRCh38)
                              6:32406171 (GRCh37)
                              Canonical SPDI:
                              NC_000006.12:32438393:T:C
                              Gene:
                              HLA-DRA (Varview)
                              Functional Consequence:
                              2KB_upstream_variant,upstream_transcript_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              C=0./0 (ALFA)
                              C=0.000008/2 (TOPMED)
                              HGVS:

                              15.

                              rs1485134229 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                T>C [Show Flanks]
                                Chromosome:
                                6:32444464 (GRCh38)
                                6:32412241 (GRCh37)
                                Canonical SPDI:
                                NC_000006.12:32444463:T:C
                                Gene:
                                HLA-DRA (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                C=0./0 (ALFA)
                                C=0.000023/6 (TOPMED)
                                HGVS:

                                16.

                                rs1484267377 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  6:32443887 (GRCh38)
                                  6:32411664 (GRCh37)
                                  Canonical SPDI:
                                  NC_000006.12:32443886:G:A
                                  Gene:
                                  HLA-DRA (Varview)
                                  Functional Consequence:
                                  coding_sequence_variant,missense_variant
                                  HGVS:

                                  17.

                                  rs1483837422 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    GA>- [Show Flanks]
                                    Chromosome:
                                    6:32439094 (GRCh38)
                                    6:32406871 (GRCh37)
                                    Canonical SPDI:
                                    NC_000006.12:32439092:AGA:A
                                    Gene:
                                    HLA-DRA (Varview)
                                    Functional Consequence:
                                    2KB_upstream_variant,upstream_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    A=0.000084/1 (ALFA)
                                    -=0.001015/126 (GnomAD)
                                    -=0.001649/27 (TOMMO)
                                    HGVS:

                                    18.

                                    rs1483320225 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>A,T [Show Flanks]
                                      Chromosome:
                                      6:32438074 (GRCh38)
                                      6:32405851 (GRCh37)
                                      Canonical SPDI:
                                      NC_000006.12:32438073:C:A,NC_000006.12:32438073:C:T
                                      Gene:
                                      HLA-DRA (Varview)
                                      Functional Consequence:
                                      2KB_upstream_variant,upstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0./0 (ALFA)
                                      T=0.000004/1 (TOPMED)
                                      HGVS:
                                      NC_000006.12:g.32438074C>A, NC_000006.12:g.32438074C>T, NC_000006.11:g.32405851C>A, NC_000006.11:g.32405851C>T, NT_113891.3:g.3876196C>A, NT_113891.3:g.3876196C>T, NT_113891.2:g.3876302C>A, NT_113891.2:g.3876302C>T, NG_002392.2:g.2407C>A, NG_002392.2:g.2407C>T, NT_167248.2:g.3661139C>A, NT_167248.2:g.3661139C>T, NT_167248.1:g.3666735C>A, NT_167248.1:g.3666735C>T, NT_167245.2:g.3678392C>A, NT_167245.2:g.3678392C>T, NT_167245.1:g.3683977C>A, NT_167245.1:g.3683977C>T, NT_167249.2:g.3753230C>A, NT_167249.2:g.3753230C>T, NT_167249.1:g.3752528C>A, NT_167249.1:g.3752528C>T, NT_167246.2:g.3742297C>A, NT_167246.2:g.3742297C>T, NT_167246.1:g.3747917C>A, NT_167246.1:g.3747917C>T, NT_167247.2:g.3779054C>A, NT_167247.2:g.3779054C>T, NT_167247.1:g.3784639C>A, NT_167247.1:g.3784639C>T, NT_187692.1:g.16659G>T, NT_187692.1:g.16659G>A

                                      19.

                                      rs1483068014 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G [Show Flanks]
                                        Chromosome:
                                        6:32441376 (GRCh38)
                                        6:32409153 (GRCh37)
                                        Canonical SPDI:
                                        NC_000006.12:32441375:A:G
                                        Gene:
                                        HLA-DRA (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000014/2 (GnomAD)
                                        G=0.000023/6 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1482527883 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>G [Show Flanks]
                                          Chromosome:
                                          6:32443268 (GRCh38)
                                          6:32411045 (GRCh37)
                                          Canonical SPDI:
                                          NC_000006.12:32443267:A:G
                                          Gene:
                                          HLA-DRA (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,missense_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          G=0.000111/1 (ALFA)
                                          G=0.000008/2 (GnomAD_exomes)
                                          HGVS:

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