List of variants in gene CDK12 reported as likely benign for Hereditary breast ovarian cancer syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_016507.4(CDK12):c.2108+56T>A	rs72827109	0.04374
NM_016507.4(CDK12):c.3824C>T (p.Pro1275Leu)	rs34070318	0.01117
NM_016507.4(CDK12):c.3584C>T (p.Thr1195Met)	rs61741615	0.01000
NM_016507.4(CDK12):c.3566T>A (p.Leu1189Gln)	rs56362165	0.00763
NM_016507.4(CDK12):c.2846+44A>G	rs8072744	0.00377
NM_016507.4(CDK12):c.2964C>T (p.Phe988=)	rs61747413	0.00279
NM_016507.4(CDK12):c.2667-12T>A	rs370484448	0.00255
NM_016507.4(CDK12):c.1932-47C>T	rs146187526	0.00103
NM_016507.4(CDK12):c.2249-32T>C	rs150596077	0.00101
NM_016507.4(CDK12):c.3024G>T (p.Arg1008=)	rs61747400	0.00101
NM_016507.4(CDK12):c.2248+61T>G	rs183044185	0.00026
NM_016507.4(CDK12):c.3286T>C (p.Ser1096Pro)	rs144011843	0.00015
NM_016507.4(CDK12):c.3308-26A>G	rs367845839	0.00007
NM_016507.4(CDK12):c.2667-80T>C	rs376592953	0.00006
NM_016507.4(CDK12):c.3315T>C (p.Ala1105=)	rs112487807	0.00002
NM_016507.4(CDK12):c.2249-36C>T	rs2145913679
NM_016507.4(CDK12):c.2847-48G>C	rs555458262
NM_016507.4(CDK12):c.2964-84G>A	rs1163669879
NM_016507.4(CDK12):c.4423C>A (p.Pro1475Thr)	rs2146852885

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