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1.

rs1491579531 has merged into rs34134152 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
    Chromosome:
    3:186243909 (GRCh38)
    3:185961698 (GRCh37)
    Canonical SPDI:
    NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
    Gene:
    DGKG (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    TTTTTTTTTTTTTT=0./0 (ALFA)
    -=0.4297/2152 (1000Genomes)
    HGVS:
    NC_000003.12:g.186243909_186243913del, NC_000003.12:g.186243910_186243913del, NC_000003.12:g.186243911_186243913del, NC_000003.12:g.186243912_186243913del, NC_000003.12:g.186243913del, NC_000003.12:g.186243913dup, NC_000003.12:g.186243912_186243913dup, NC_000003.12:g.186243896_186243913T[20]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.186243911_186243913dup, NC_000003.12:g.186243910_186243913dup, NC_000003.12:g.186243909_186243913dup, NC_000003.12:g.186243908_186243913dup, NC_000003.12:g.186243907_186243913dup, NC_000003.12:g.186243906_186243913dup, NC_000003.12:g.186243896_186243913T[26]GTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.186243905_186243913dup, NC_000003.12:g.186243904_186243913dup, NC_000003.12:g.186243903_186243913dup, NC_000003.12:g.186243902_186243913dup, NC_000003.12:g.186243901_186243913dup, NC_000003.12:g.186243900_186243913dup, NC_000003.12:g.186243899_186243913dup, NC_000003.12:g.186243898_186243913dup, NC_000003.12:g.186243897_186243913dup, NC_000003.12:g.186243896_186243913dup, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961698_185961702del, NC_000003.11:g.185961699_185961702del, NC_000003.11:g.185961700_185961702del, NC_000003.11:g.185961701_185961702del, NC_000003.11:g.185961702del, NC_000003.11:g.185961702dup, NC_000003.11:g.185961701_185961702dup, NC_000003.11:g.185961685_185961702T[20]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.185961700_185961702dup, NC_000003.11:g.185961699_185961702dup, NC_000003.11:g.185961698_185961702dup, NC_000003.11:g.185961697_185961702dup, NC_000003.11:g.185961696_185961702dup, NC_000003.11:g.185961695_185961702dup, NC_000003.11:g.185961685_185961702T[26]GTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.185961694_185961702dup, NC_000003.11:g.185961693_185961702dup, NC_000003.11:g.185961692_185961702dup, NC_000003.11:g.185961691_185961702dup, NC_000003.11:g.185961690_185961702dup, NC_000003.11:g.185961689_185961702dup, NC_000003.11:g.185961688_185961702dup, NC_000003.11:g.185961687_185961702dup, NC_000003.11:g.185961686_185961702dup, NC_000003.11:g.185961685_185961702dup, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

    2.

    rs1491578606 has merged into rs1491157719 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TCTC>-,TC,TCTCTC,TCTCTCTC,TCTCTCTCTC [Show Flanks]
      Chromosome:
      3:186297066 (GRCh38)
      3:186014855 (GRCh37)
      Canonical SPDI:
      NC_000003.12:186297061:TCTCTCTC:TCTC,NC_000003.12:186297061:TCTCTCTC:TCTCTC,NC_000003.12:186297061:TCTCTCTC:TCTCTCTCTC,NC_000003.12:186297061:TCTCTCTC:TCTCTCTCTCTC,NC_000003.12:186297061:TCTCTCTC:TCTCTCTCTCTCTC
      Gene:
      DGKG (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      TCTCTC=0./0 (ALFA)
      TC=0.00011/2 (TOMMO)
      HGVS:

      3.

      rs1491535048 has merged into rs34134152 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
        Chromosome:
        3:186243909 (GRCh38)
        3:185961698 (GRCh37)
        Canonical SPDI:
        NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186243895:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
        Gene:
        DGKG (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        TTTTTTTTTTTTTT=0./0 (ALFA)
        -=0.4297/2152 (1000Genomes)
        HGVS:
        NC_000003.12:g.186243909_186243913del, NC_000003.12:g.186243910_186243913del, NC_000003.12:g.186243911_186243913del, NC_000003.12:g.186243912_186243913del, NC_000003.12:g.186243913del, NC_000003.12:g.186243913dup, NC_000003.12:g.186243912_186243913dup, NC_000003.12:g.186243896_186243913T[20]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.186243911_186243913dup, NC_000003.12:g.186243910_186243913dup, NC_000003.12:g.186243909_186243913dup, NC_000003.12:g.186243908_186243913dup, NC_000003.12:g.186243907_186243913dup, NC_000003.12:g.186243906_186243913dup, NC_000003.12:g.186243896_186243913T[26]GTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.186243905_186243913dup, NC_000003.12:g.186243904_186243913dup, NC_000003.12:g.186243903_186243913dup, NC_000003.12:g.186243902_186243913dup, NC_000003.12:g.186243901_186243913dup, NC_000003.12:g.186243900_186243913dup, NC_000003.12:g.186243899_186243913dup, NC_000003.12:g.186243898_186243913dup, NC_000003.12:g.186243897_186243913dup, NC_000003.12:g.186243896_186243913dup, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.186243913_186243914insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961698_185961702del, NC_000003.11:g.185961699_185961702del, NC_000003.11:g.185961700_185961702del, NC_000003.11:g.185961701_185961702del, NC_000003.11:g.185961702del, NC_000003.11:g.185961702dup, NC_000003.11:g.185961701_185961702dup, NC_000003.11:g.185961685_185961702T[20]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.185961700_185961702dup, NC_000003.11:g.185961699_185961702dup, NC_000003.11:g.185961698_185961702dup, NC_000003.11:g.185961697_185961702dup, NC_000003.11:g.185961696_185961702dup, NC_000003.11:g.185961695_185961702dup, NC_000003.11:g.185961685_185961702T[26]GTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.185961694_185961702dup, NC_000003.11:g.185961693_185961702dup, NC_000003.11:g.185961692_185961702dup, NC_000003.11:g.185961691_185961702dup, NC_000003.11:g.185961690_185961702dup, NC_000003.11:g.185961689_185961702dup, NC_000003.11:g.185961688_185961702dup, NC_000003.11:g.185961687_185961702dup, NC_000003.11:g.185961686_185961702dup, NC_000003.11:g.185961685_185961702dup, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.185961702_185961703insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

        4.

        rs1491519550 has merged into rs56211107 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          CTCACTCACTCACTCACTCACTCA>-,CTCA,CTCACTCA,CTCACTCACTCA,CTCACTCACTCACTCA,CTCACTCACTCACTCACTCA,CTCACTCACTCACTCACTCACTCACTCA,CTCACTCACTCACTCACTCACTCACTCACTCA,CTCACTCACTCACTCACTCACTCACTCACTCACTCA,CTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA [Show Flanks]
          Chromosome:
          3:186167780 (GRCh38)
          3:185885569 (GRCh37)
          Canonical SPDI:
          NC_000003.12:186167760:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA:TCACTCACTCACTCACTCA,NC_000003.12:186167760:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA:TCACTCACTCACTCACTCACTCA,NC_000003.12:186167760:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA:TCACTCACTCACTCACTCACTCACTCA,NC_000003.12:186167760:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA:TCACTCACTCACTCACTCACTCACTCACTCA,NC_000003.12:186167760:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA:TCACTCACTCACTCACTCACTCACTCACTCACTCA,NC_000003.12:186167760:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCA,NC_000003.12:186167760:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA,NC_000003.12:186167760:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA,NC_000003.12:186167760:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA,NC_000003.12:186167760:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA:TCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCACTCA
          Gene:
          DGKG (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          TCACTCACTCACTCACTCACTCA=0./0 (ALFA)
          -=0.35/14 (GENOME_DK)
          -=0.3832/1695 (1000Genomes)
          HGVS:

          5.

          rs1491504507 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            ->CACAGAGTATTT [Show Flanks]
            Chromosome:
            3:186312161 (GRCh38)
            3:186029951 (GRCh37)
            Canonical SPDI:
            NC_000003.12:186312161:CACAGAGTATTT:CACAGAGTATTTCACAGAGTATTT
            Gene:
            DGKG (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            CACAGAGTATTTCACAGAGTATTT=0./0 (ALFA)
            HGVS:

            6.

            rs1491498749 [Homo sapiens]
              Variant type:
              SNV:
              Alleles:
              ->GTGTGAGTGTGTGTGTGTGTGTGT
              Chromosome:
              no mapping
              Canonical SPDI:

              7.

              rs1491497675 [Homo sapiens]
                Variant type:
                SNV:
                Alleles:
                ->TAAAA
                Chromosome:
                no mapping
                Canonical SPDI:

                8.

                rs1491486804 has merged into rs34266987 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  TTT>-,T,TT,TTTT,TTTTT,TTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
                  Chromosome:
                  3:186263668 (GRCh38)
                  3:185981457 (GRCh37)
                  Canonical SPDI:
                  NC_000003.12:186263655:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:186263655:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:186263655:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:186263655:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:186263655:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:186263655:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:186263655:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:186263655:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
                  Gene:
                  DGKG (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  TTTTTTTTTTTTT=0./0 (ALFA)
                  HGVS:

                  9.

                  rs1491461291 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AG>- [Show Flanks]
                    Chromosome:
                    3:186164534 (GRCh38)
                    3:185882323 (GRCh37)
                    Canonical SPDI:
                    NC_000003.12:186164531:AGAG:AG
                    Gene:
                    DGKG (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    AGAG=0./0 (ALFA)
                    -=0.000004/1 (TOPMED)
                    HGVS:

                    10.

                    rs1491455928 has merged into rs1423343682 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      AA>-,AAAA [Show Flanks]
                      Chromosome:
                      3:186148978 (GRCh38)
                      3:185866767 (GRCh37)
                      Canonical SPDI:
                      NC_000003.12:186148976:AAA:A,NC_000003.12:186148976:AAA:AAAAA
                      Gene:
                      DGKG (Varview)
                      Functional Consequence:
                      3_prime_UTR_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      AAAAA=0./0 (ALFA)
                      -=0.00011/3 (TOMMO)
                      HGVS:

                      11.

                      rs1491455132 [Homo sapiens]
                        Variant type:
                        SNV:
                        Alleles:
                        ->ATATATAGATATATATATATATATATATAT
                        Chromosome:
                        no mapping
                        Canonical SPDI:

                        12.

                        rs1491452250 has merged into rs34829528 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          AAAAAAAAAAAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                          Chromosome:
                          3:186295649 (GRCh38)
                          3:186013438 (GRCh37)
                          Canonical SPDI:
                          NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186295638:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                          Gene:
                          DGKG (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          AAAAAAAAAA=0./0 (ALFA)
                          -=0.375/15 (GENOME_DK)
                          HGVS:
                          NC_000003.12:g.186295649_186295660del, NC_000003.12:g.186295650_186295660del, NC_000003.12:g.186295651_186295660del, NC_000003.12:g.186295653_186295660del, NC_000003.12:g.186295654_186295660del, NC_000003.12:g.186295655_186295660del, NC_000003.12:g.186295656_186295660del, NC_000003.12:g.186295658_186295660del, NC_000003.12:g.186295659_186295660del, NC_000003.12:g.186295660del, NC_000003.12:g.186295660dup, NC_000003.12:g.186295659_186295660dup, NC_000003.12:g.186295658_186295660dup, NC_000003.12:g.186295657_186295660dup, NC_000003.12:g.186295656_186295660dup, NC_000003.12:g.186295655_186295660dup, NC_000003.12:g.186295654_186295660dup, NC_000003.12:g.186295653_186295660dup, NC_000003.12:g.186295652_186295660dup, NC_000003.12:g.186295651_186295660dup, NC_000003.12:g.186295650_186295660dup, NC_000003.12:g.186295649_186295660dup, NC_000003.12:g.186295648_186295660dup, NC_000003.12:g.186295647_186295660dup, NC_000003.12:g.186295646_186295660dup, NC_000003.12:g.186295645_186295660dup, NC_000003.12:g.186295644_186295660dup, NC_000003.12:g.186295643_186295660dup, NC_000003.12:g.186295640_186295660dup, NC_000003.12:g.186295639_186295660dup, NC_000003.12:g.186295660_186295661insAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.186295660_186295661insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.186295660_186295661insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.186295660_186295661insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.186295660_186295661insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.186295660_186295661insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.186295660_186295661insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.186295660_186295661insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.186295660_186295661insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.186295660_186295661insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.186295639_186295660A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000003.11:g.186013438_186013449del, NC_000003.11:g.186013439_186013449del, NC_000003.11:g.186013440_186013449del, NC_000003.11:g.186013442_186013449del, NC_000003.11:g.186013443_186013449del, NC_000003.11:g.186013444_186013449del, NC_000003.11:g.186013445_186013449del, NC_000003.11:g.186013447_186013449del, NC_000003.11:g.186013448_186013449del, NC_000003.11:g.186013449del, NC_000003.11:g.186013449dup, NC_000003.11:g.186013448_186013449dup, NC_000003.11:g.186013447_186013449dup, NC_000003.11:g.186013446_186013449dup, NC_000003.11:g.186013445_186013449dup, NC_000003.11:g.186013444_186013449dup, NC_000003.11:g.186013443_186013449dup, NC_000003.11:g.186013442_186013449dup, NC_000003.11:g.186013441_186013449dup, NC_000003.11:g.186013440_186013449dup, NC_000003.11:g.186013439_186013449dup, NC_000003.11:g.186013438_186013449dup, NC_000003.11:g.186013437_186013449dup, NC_000003.11:g.186013436_186013449dup, NC_000003.11:g.186013435_186013449dup, NC_000003.11:g.186013434_186013449dup, NC_000003.11:g.186013433_186013449dup, NC_000003.11:g.186013432_186013449dup, NC_000003.11:g.186013429_186013449dup, NC_000003.11:g.186013428_186013449dup, NC_000003.11:g.186013449_186013450insAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.186013449_186013450insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.186013449_186013450insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.186013449_186013450insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.186013449_186013450insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.186013449_186013450insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.186013449_186013450insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.186013449_186013450insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.186013449_186013450insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.186013449_186013450insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.186013428_186013449A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

                          13.

                          rs1491450682 has merged into rs1161706511 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            AAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA [Show Flanks]
                            Chromosome:
                            3:186314768 (GRCh38)
                            3:186032557 (GRCh37)
                            Canonical SPDI:
                            NC_000003.12:186314753:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:186314753:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:186314753:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000003.12:186314753:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:186314753:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186314753:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186314753:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:186314753:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
                            Gene:
                            DGKG (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            AAAAAAAAAAAAAAAAAA=0./0 (ALFA)
                            -=0.000004/1 (TOPMED)
                            HGVS:

                            14.

                            rs1491444855 has merged into rs11288455 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              AAAA>-,AA,AAA [Show Flanks]
                              Chromosome:
                              3:186208449 (GRCh38)
                              3:185926238 (GRCh37)
                              Canonical SPDI:
                              NC_000003.12:186208442:AAAAAAAAAA:AAAAAA,NC_000003.12:186208442:AAAAAAAAAA:AAAAAAAA,NC_000003.12:186208442:AAAAAAAAAA:AAAAAAAAA
                              Gene:
                              DGKG (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              AAAAAAAA=0./0 (ALFA)
                              A=0./0 (ALSPAC)
                              A=0./0 (TWINSUK)
                              A=0.001/1 (GoNL)
                              A=0.07177/1203 (TOMMO)
                              A=0.075/3 (GENOME_DK)
                              A=0.14101/706 (1000Genomes)
                              HGVS:

                              15.

                              rs1491395003 has merged into rs142522791 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                GTGT>-,GT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
                                Chromosome:
                                3:186358522 (GRCh38)
                                3:186076311 (GRCh37)
                                Canonical SPDI:
                                NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000003.12:186358506:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
                                Gene:
                                DGKG (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                TGTGTGTGTGTGTGTGT=0./0 (ALFA)
                                TGTGTGTGTGTGTGTG=0.0182/91 (1000Genomes)
                                -=0.475/19 (GENOME_DK)
                                HGVS:
                                NC_000003.12:g.186358508GT[7], NC_000003.12:g.186358508GT[8], NC_000003.12:g.186358508GT[10], NC_000003.12:g.186358508GT[11], NC_000003.12:g.186358508GT[12], NC_000003.12:g.186358508GT[13], NC_000003.12:g.186358508GT[14], NC_000003.12:g.186358508GT[15], NC_000003.12:g.186358508GT[16], NC_000003.12:g.186358508GT[17], NC_000003.12:g.186358508GT[18], NC_000003.12:g.186358508GT[19], NC_000003.12:g.186358508GT[20], NC_000003.12:g.186358508GT[21], NC_000003.12:g.186358508GT[22], NC_000003.12:g.186358508GT[23], NC_000003.12:g.186358508GT[24], NC_000003.12:g.186358508GT[25], NC_000003.11:g.186076297GT[7], NC_000003.11:g.186076297GT[8], NC_000003.11:g.186076297GT[10], NC_000003.11:g.186076297GT[11], NC_000003.11:g.186076297GT[12], NC_000003.11:g.186076297GT[13], NC_000003.11:g.186076297GT[14], NC_000003.11:g.186076297GT[15], NC_000003.11:g.186076297GT[16], NC_000003.11:g.186076297GT[17], NC_000003.11:g.186076297GT[18], NC_000003.11:g.186076297GT[19], NC_000003.11:g.186076297GT[20], NC_000003.11:g.186076297GT[21], NC_000003.11:g.186076297GT[22], NC_000003.11:g.186076297GT[23], NC_000003.11:g.186076297GT[24], NC_000003.11:g.186076297GT[25]

                                16.

                                rs1491392715 has merged into rs1246127568 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  CACA>-,CA,CACACA [Show Flanks]
                                  Chromosome:
                                  3:186302559 (GRCh38)
                                  3:186020348 (GRCh37)
                                  Canonical SPDI:
                                  NC_000003.12:186302557:ACACA:A,NC_000003.12:186302557:ACACA:ACA,NC_000003.12:186302557:ACACA:ACACACA
                                  Gene:
                                  DGKG (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  ACA=0./0 (ALFA)
                                  HGVS:

                                  17.

                                  rs1491378745 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    ->GAG [Show Flanks]
                                    Chromosome:
                                    3:186164532 (GRCh38)
                                    3:185882322 (GRCh37)
                                    Canonical SPDI:
                                    NC_000003.12:186164532:GAG:GAGGAG
                                    Gene:
                                    DGKG (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    GAGGAG=0./0 (ALFA)
                                    GAG=0.000007/1 (GnomAD)
                                    HGVS:

                                    18.

                                    rs1491365354 [Homo sapiens]
                                      Variant type:
                                      DEL
                                      Alleles:
                                      CA>- [Show Flanks]
                                      Chromosome:
                                      3:186323936 (GRCh38)
                                      3:186041725 (GRCh37)
                                      Canonical SPDI:
                                      NC_000003.12:186323935:CA:
                                      Gene:
                                      DGKG (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      -=0./0 (ALFA)
                                      HGVS:

                                      19.

                                      rs1491362723 has merged into rs753836088 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        GAGA>-,GA,GAGAGA [Show Flanks]
                                        Chromosome:
                                        3:186260547 (GRCh38)
                                        3:185978336 (GRCh37)
                                        Canonical SPDI:
                                        NC_000003.12:186260538:GAGAGAGAGAGA:GAGAGAGA,NC_000003.12:186260538:GAGAGAGAGAGA:GAGAGAGAGA,NC_000003.12:186260538:GAGAGAGAGAGA:GAGAGAGAGAGAGA
                                        Gene:
                                        DGKG (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        GAGAGAGAGAGAGA=0./0 (ALFA)
                                        -=0.00021/4 (TOMMO)
                                        -=0.00109/2 (Korea1K)
                                        HGVS:

                                        20.

                                        rs1491361398 [Homo sapiens]
                                          Variant type:
                                          DELINS
                                          Alleles:
                                          ->GAAAAAAA [Show Flanks]
                                          Chromosome:
                                          3:186296112 (GRCh38)
                                          3:186013902 (GRCh37)
                                          Canonical SPDI:
                                          NC_000003.12:186296112:AAAAA:AAAAAGAAAAAAA
                                          Gene:
                                          DGKG (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          AAAAAGAAAAAAA=0./0 (ALFA)
                                          AAAAAGAA=0.000076/10 (GnomAD)
                                          HGVS:

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