ClinVar Miner

List of variants in gene CDK12 reported as not provided

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Total variants: 17
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HGVS dbSNP
NM_016507.4(CDK12):c.1579C>A (p.Pro527Thr) rs587778182
NM_016507.4(CDK12):c.1705_1707del (p.Ser569del) rs587778181
NM_016507.4(CDK12):c.1855A>G (p.Ile619Val) rs144501352
NM_016507.4(CDK12):c.1913G>C (p.Gly638Ala) rs587778183
NM_016507.4(CDK12):c.1988G>A (p.Arg663His) rs141353560
NM_016507.4(CDK12):c.2964C>T (p.Phe988=) rs61747413
NM_016507.4(CDK12):c.3391A>G (p.Ile1131Val) rs61747430
NM_016507.4(CDK12):c.3566T>A (p.Leu1189Gln) rs56362165
NM_016507.4(CDK12):c.3569C>G (p.Pro1190Arg) rs587778177
NM_016507.4(CDK12):c.3584C>T (p.Thr1195Met) rs61741615
NM_016507.4(CDK12):c.3824C>T (p.Pro1275Leu) rs34070318
NM_016507.4(CDK12):c.3859T>G (p.Ser1287Ala) rs587778179
NM_016507.4(CDK12):c.3997C>T (p.Arg1333Cys) rs142347393
NM_016507.4(CDK12):c.4276A>G (p.Ser1426Gly) rs587778178
NM_016507.4(CDK12):c.4381G>T (p.Gly1461Cys) rs186043011
NM_016507.4(CDK12):c.4402T>C (p.Tyr1468His) rs587778180
NM_016507.4(CDK12):c.4415A>G (p.Tyr1472Cys) rs373240630

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