"PreventionGenetics, part of Exact Sciences"[submitter] AND "CDK12"[ge - ClinVar

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Items: 22

	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 disorder	GBenign
Select item 3055556	NM_016507.4(CDK12):c.267C>T (p.Phe89=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	CDK12-related disorder	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 disorder	GLikely benign
Select item 1250047	NM_016507.4(CDK12):c.714G>A (p.Ser238=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	Hereditary breast ovarian cancer syndrome +2 more	GBenign
Select item 3035867	NM_016507.4(CDK12):c.912C>G (p.Pro304=)	CDK12, LOC126862553	Single nucleotide variant (synonymous variant)	CDK12-related disorder	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
Select item 3040105	NM_016507.4(CDK12):c.1248T>C (p.Asp416=)	CDK12	Single nucleotide variant (synonymous variant)	CDK12-related disorder	GLikely benign
Select item 1678982	NM_016507.4(CDK12):c.1302A>G (p.Ser434=)	CDK12	Single nucleotide variant (synonymous variant)	Hereditary breast ovarian cancer syndrome +1 more	GBenign
Select item 3042823	NM_016507.4(CDK12):c.1815A>G (p.Val605=)	CDK12	Single nucleotide variant (synonymous variant)	CDK12-related disorder	GLikely benign
Select item 3039024	NM_016507.4(CDK12):c.2892C>A (p.Ile964=)	CDK12	Single nucleotide variant (synonymous variant)	CDK12-related disorder	GLikely benign
Select item 133856	NM_016507.4(CDK12):c.2964C>T (p.Phe988=)	CDK12	Single nucleotide variant (synonymous variant)	CDK12-related disorder +1 more	GBenign/Likely benign
Select item 1678992	NM_016507.4(CDK12):c.3024G>T (p.Arg1008=)	CDK12	Single nucleotide variant (synonymous variant)	Hereditary breast ovarian cancer syndrome +1 more	GLikely benign
Select item 3034908	NM_016507.4(CDK12):c.3051C>T (p.Ser1017=)	CDK12	Single nucleotide variant (synonymous variant)	CDK12-related disorder	GLikely benign
Select item 3028958	NM_016507.4(CDK12):c.3075C>T (p.Leu1025=)	CDK12	Single nucleotide variant (synonymous variant)	CDK12-related disorder	GLikely benign
Select item 133857	NM_016507.4(CDK12):c.3391A>G (p.Ile1131Val)	CDK12 (I1131V)	Single nucleotide variant (missense variant)	CDK12-related disorder +1 more	GBenign
Select item 1222232	NM_016507.4(CDK12):c.3483G>A (p.Thr1161=)	CDK12	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 133860	NM_016507.4(CDK12):c.3566T>A (p.Leu1189Gln)	CDK12 (L1189Q)	Single nucleotide variant (missense variant)	CDK12-related disorder +1 more	GBenign/Likely benign
Select item 133859	NM_016507.4(CDK12):c.3584C>T (p.Thr1195Met)	CDK12 (T1195M)	Single nucleotide variant (missense variant)	CDK12-related disorder +1 more	GBenign/Likely benign
Select item 3043246	NM_016507.4(CDK12):c.3717G>A (p.Gln1239=)	CDK12	Single nucleotide variant (synonymous variant)	CDK12-related disorder	GLikely benign
Select item 133863	NM_016507.4(CDK12):c.3824C>T (p.Pro1275Leu)	CDK12 (P1266L +1 more)	Single nucleotide variant (missense variant)	CDK12-related disorder +1 more	GBenign/Likely benign
Select item 3052381	NM_016507.4(CDK12):c.3839C>T (p.Pro1280Leu)	CDK12 (P1271L +1 more)	Single nucleotide variant (missense variant)	CDK12-related disorder	GLikely benign

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Items: 22