ClinVar Miner

List of variants in gene CYP2C19 studied for not provided

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_000769.1(CYP2C19):c.991A>G (p.Ile331Val) rs3758581 0.95515
NM_000769.4(CYP2C19):c.99C>T (p.Pro33=) rs17885098 0.92070
NM_000769.4(CYP2C19):c.681G>A (p.Pro227=) rs4244285 0.16148
NM_000769.4(CYP2C19):c.1251A>C (p.Gly417=) rs17886522 0.00780
CYP2C19*15 rs17882687 0.00626
NM_000769.1(CYP2C19):c.431G>A (p.Arg144His) rs17884712 0.00391
CYP2C19*11 rs58973490 0.00302
NM_000769.1(CYP2C19):c.358T>C (p.Trp120Arg) rs41291556 0.00159
NM_000769.1(CYP2C19):c.1A>G (p.Met1Val) rs28399504 0.00156
NM_000769.1(CYP2C19):c.636G>A (p.Trp212Ter) rs4986893 0.00149
NM_000769.1(CYP2C19):c.1297C>T (p.Arg433Trp) rs56337013 0.00001
NM_000769.4(CYP2C19):c.1173C>A (p.Leu391=) rs935030527 0.00001
GRCh37/hg19 10q23.33(chr10:96497260-96558710)x1
GRCh37/hg19 10q23.33(chr10:96501534-96548712)x1
GRCh37/hg19 10q23.33(chr10:96502305-96562508)x1
GRCh37/hg19 10q23.33(chr10:96528208-96541982)x1
GRCh37/hg19 10q23.33(chr10:96533912-96598380)x1
GRCh37/hg19 10q23.33(chr10:96534277-96599102)x1
GRCh37/hg19 10q23.33(chr10:96541982-96602398)x0
GRCh37/hg19 10q23.33(chr10:96541982-96647117)x0
GRCh37/hg19 10q23.33(chr10:96558287-96606761)x1
GRCh37/hg19 10q23.33(chr10:96562918-96606761)x1
NM_000769.4(CYP2C19):c.1059C>T (p.His353=)

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