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1.

rs3762836 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>A,C [Show Flanks]
    Chromosome:
    4:55444700 (GRCh38)
    4:56310867 (GRCh37)
    Canonical SPDI:
    NC_000004.12:55444699:T:A,NC_000004.12:55444699:T:C
    Gene:
    CLOCK (Varview), TMEM165 (Varview)
    Functional Consequence:
    intron_variant,missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.00002/1 (ALFA)
    C=0./0 (HapMap)
    A=0.00008/1 (GoESP)
    C=0.00234/15 (1000Genomes_30X)
    C=0.0024/12 (1000Genomes)
    C=0.00812/5 (Vietnamese)
    C=0.01146/21 (Korea1K)
    C=0.01327/96 (Korea4K)
    C=0.01404/1087 (TOMMO)
    C=0.01506/44 (KOREAN)
    T=0.5/3 (SGDP_PRJ)
    HGVS:
    NC_000004.12:g.55444700T>A, NC_000004.12:g.55444700T>C, NC_000004.11:g.56310867T>A, NC_000004.11:g.56310867T>C, NG_032881.2:g.53745T>A, NG_032881.2:g.53745T>C, NM_004898.4:c.1625A>T, NM_004898.4:c.1625A>G, NM_004898.3:c.1625A>T, NM_004898.3:c.1625A>G, XM_005265787.3:c.1625A>T, XM_005265787.3:c.1625A>G, XM_005265787.2:c.1625A>T, XM_005265787.2:c.1625A>G, XM_005265787.1:c.1625A>T, XM_005265787.1:c.1625A>G, XM_011534411.3:c.1625A>T, XM_011534411.3:c.1625A>G, XM_011534411.2:c.1625A>T, XM_011534411.2:c.1625A>G, XM_011534411.1:c.1625A>T, XM_011534411.1:c.1625A>G, XM_011534410.3:c.1625A>T, XM_011534410.3:c.1625A>G, XM_011534410.2:c.1625A>T, XM_011534410.2:c.1625A>G, XM_011534410.1:c.1625A>T, XM_011534410.1:c.1625A>G, NM_001267843.2:c.1625A>T, NM_001267843.2:c.1625A>G, NM_001267843.1:c.1625A>T, NM_001267843.1:c.1625A>G, XM_024454284.2:c.1625A>T, XM_024454284.2:c.1625A>G, XM_024454284.1:c.1625A>T, XM_024454284.1:c.1625A>G, XM_017008854.2:c.1625A>T, XM_017008854.2:c.1625A>G, XM_017008854.1:c.1625A>T, XM_017008854.1:c.1625A>G, XM_047416434.1:c.1625A>T, XM_047416434.1:c.1625A>G, XM_047416433.1:c.1625A>T, XM_047416433.1:c.1625A>G, XM_047416437.1:c.1625A>T, XM_047416437.1:c.1625A>G, XM_047416436.1:c.1625A>T, XM_047416436.1:c.1625A>G, XM_047416438.1:c.1625A>T, XM_047416438.1:c.1625A>G, XM_047416431.1:c.1625A>T, XM_047416431.1:c.1625A>G, XM_047416435.1:c.1625A>T, XM_047416435.1:c.1625A>G, XM_047416439.1:c.1625A>T, XM_047416439.1:c.1625A>G, XM_047416432.1:c.1625A>T, XM_047416432.1:c.1625A>G, XM_047416440.1:c.1625A>T, XM_047416440.1:c.1625A>G, NP_004889.1:p.His542Leu, NP_004889.1:p.His542Arg, XP_005265844.1:p.His542Leu, XP_005265844.1:p.His542Arg, XP_011532713.1:p.His542Leu, XP_011532713.1:p.His542Arg, XP_011532712.1:p.His542Leu, XP_011532712.1:p.His542Arg, NP_001254772.1:p.His542Leu, NP_001254772.1:p.His542Arg, XP_024310052.1:p.His542Leu, XP_024310052.1:p.His542Arg, XP_016864343.1:p.His542Leu, XP_016864343.1:p.His542Arg, XP_047272390.1:p.His542Leu, XP_047272390.1:p.His542Arg, XP_047272389.1:p.His542Leu, XP_047272389.1:p.His542Arg, XP_047272393.1:p.His542Leu, XP_047272393.1:p.His542Arg, XP_047272392.1:p.His542Leu, XP_047272392.1:p.His542Arg, XP_047272394.1:p.His542Leu, XP_047272394.1:p.His542Arg, XP_047272387.1:p.His542Leu, XP_047272387.1:p.His542Arg, XP_047272391.1:p.His542Leu, XP_047272391.1:p.His542Arg, XP_047272395.1:p.His542Leu, XP_047272395.1:p.His542Arg, XP_047272388.1:p.His542Leu, XP_047272388.1:p.His542Arg, XP_047272396.1:p.His542Leu, XP_047272396.1:p.His542Arg

    PubMed

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