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1.

rs1801127 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    3:9751101 (GRCh38)
    3:9792785 (GRCh37)
    Canonical SPDI:
    NC_000003.12:9751100:G:A
    Gene:
    OGG1 (Varview)
    Functional Consequence:
    synonymous_variant,coding_sequence_variant,intron_variant,non_coding_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0./0 (ALFA)
    A=0./0 (HapMap)
    A=0.000034/9 (TOPMED)
    A=0.0001072/16 (GnomAD_genomes)
    A=0.000133/16 (ExAC)
    A=0.0002833/397 (GnomAD_exomes)
    A=0.0081878/15 (Korea1K)
    A=0.0092402/27 (KOREAN)
    A=0.0102295/74 (Korea4K)
    A=0.0189169/1465 (TOMMO)
    HGVS:
    NC_000003.12:g.9751101G>A, NC_000003.11:g.9792785G>A, NG_012106.2:g.6151G>A, NG_012106.1:g.6158G>A, NM_002542.6:c.294G>A, NM_002542.5:c.294G>A, NM_016819.4:c.294G>A, NM_016819.3:c.294G>A, NM_016820.4:c.294G>A, NM_016820.3:c.294G>A, NM_016828.3:c.294G>A, NM_016828.2:c.294G>A, NM_016829.3:c.294G>A, NM_016829.2:c.294G>A, NM_016821.3:c.294G>A, NM_016821.2:c.294G>A, NM_016826.3:c.294G>A, NM_016826.2:c.294G>A, NM_016827.3:c.294G>A, NM_016827.2:c.294G>A, NM_001354651.2:c.294G>A, NM_001354651.1:c.294G>A, NM_001354652.2:c.294G>A, NM_001354652.1:c.294G>A, NM_001354650.2:c.294G>A, NM_001354650.1:c.294G>A, NR_148932.2:n.629G>A, NR_148932.1:n.637G>A, NM_001354648.2:c.294G>A, NM_001354648.1:c.294G>A, NM_001354649.2:c.294G>A, NM_001354649.1:c.294G>A, XM_017006494.3:c.294G>A, XM_017006494.2:c.294G>A, XM_017006494.1:c.294G>A, XM_017006495.3:c.294G>A, XM_017006495.2:c.294G>A, XM_017006495.1:c.294G>A, XM_017006493.3:c.294G>A, XM_017006493.2:c.294G>A, XM_017006493.1:c.294G>A, XM_017006497.3:c.294G>A, XM_017006497.2:c.294G>A, XM_017006497.1:c.294G>A, XM_047448201.1:c.294G>A, XM_047448200.1:c.294G>A, XM_047448202.1:c.294G>A, XM_047448203.1:c.294G>A

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