"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC126862 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3038610	NM_016507.4(CDK12):c.234T>A (p.Ser78=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	CDK12-related condition	GBenign
Select item 3055556	NM_016507.4(CDK12):c.267C>T (p.Phe89=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	CDK12-related condition	GLikely benign
Select item 1678978	NM_016507.4(CDK12):c.271C>T (p.Leu91=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	Hereditary breast ovarian cancer syndrome +1 more	GBenign/Likely benign
Select item 3042423	NM_016507.4(CDK12):c.384C>T (p.Thr128=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	CDK12-related condition	GLikely 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 3035867	NM_016507.4(CDK12):c.912C>G (p.Pro304=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	CDK12-related condition	GLikely benign
Select item 1678981	NM_016507.4(CDK12):c.966A>G (p.Arg322=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	Hereditary breast ovarian cancer syndrome +1 more	GLikely benign

ClinVar