"National Health Laboratory Service, Universitas Academic Hospital and - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1678976	NM_016507.4(CDK12):c.-27T>C	CDK12, LOC126862553	Single nucleotide variant (5 prime UTR variant)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678977	NM_016507.4(CDK12):c.-20T>C	CDK12, LOC126862553	Single nucleotide variant (5 prime UTR variant)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678978	NM_016507.4(CDK12):c.271C>T (p.Leu91=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	CDK12-related disorder +1 more	GBenign/Likely benign
Select item 1250047	NM_016507.4(CDK12):c.714G>A (p.Ser238=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1678980	NM_016507.4(CDK12):c.807C>T (p.Thr269=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678981	NM_016507.4(CDK12):c.966A>G (p.Arg322=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	CDK12-related disorder +1 more	GLikely benign

ClinVar