"Ambry Genetics"[submitter] AND "ENTPD6"[gene] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3089101	NM_001247.5(ENTPD6):c.47T>C (p.Ile16Thr)	ENTPD6 (I16T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3089102	NM_001247.5(ENTPD6):c.66C>A (p.His22Gln)	ENTPD6 (H5Q +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2513484	NM_001247.5(ENTPD6):c.158T>C (p.Val53Ala)	ENTPD6 (V36A +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2220492	NM_001247.5(ENTPD6):c.163A>G (p.Ile55Val)	ENTPD6 (I38V +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2235830	NM_001247.5(ENTPD6):c.199G>A (p.Ala67Thr)	ENTPD6 (A50T +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3275554	NM_001247.5(ENTPD6):c.230C>G (p.Ala77Gly)	ENTPD6 (A60G +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3089100	NM_001247.5(ENTPD6):c.241G>C (p.Ala81Pro)	ENTPD6 (A78P +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2590788	NM_001247.5(ENTPD6):c.307G>A (p.Gly103Arg)	ENTPD6 (G100R +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2549936	NM_001247.5(ENTPD6):c.347A>C (p.His116Pro)	ENTPD6 (H115P +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2403813	NM_001247.5(ENTPD6):c.386C>T (p.Thr129Met)	ENTPD6 (T111M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401475	NM_001247.5(ENTPD6):c.557G>A (p.Arg186His)	ENTPD6 (R183H +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2527138	NM_001247.5(ENTPD6):c.644G>A (p.Cys215Tyr)	ENTPD6 (C167Y +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3089103	NM_001247.5(ENTPD6):c.716T>G (p.Leu239Trp)	ENTPD6 (L174W +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089105	NM_001247.5(ENTPD6):c.778G>A (p.Ala260Thr)	ENTPD6 (A212T +7 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3089106	NM_001247.5(ENTPD6):c.783C>G (p.Phe261Leu)	ENTPD6 (F196L +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089107	NM_001247.5(ENTPD6):c.790C>T (p.Arg264Cys)	ENTPD6 (R246C +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356629	NM_001247.5(ENTPD6):c.791G>A (p.Arg264His)	ENTPD6 (R199H +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282825	NM_001247.5(ENTPD6):c.842G>A (p.Arg281Gln)	ENTPD6 (R264Q +7 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3089108	NM_001247.5(ENTPD6):c.892G>A (p.Gly298Arg)	ENTPD6 (G295R +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396065	NM_001247.5(ENTPD6):c.947A>T (p.Lys316Met)	ENTPD6 (K268M +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3089097	NM_001247.5(ENTPD6):c.1060G>A (p.Glu354Lys)	ENTPD6 (E102K +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275551	NM_001247.5(ENTPD6):c.1102G>A (p.Val368Met)	ENTPD6 (V303M +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089098	NM_001247.5(ENTPD6):c.1112C>T (p.Thr371Met)	ENTPD6 (T153M +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402858	NM_001247.5(ENTPD6):c.1159G>A (p.Asp387Asn)	ENTPD6 (D169N +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559954	NM_001247.5(ENTPD6):c.1169C>T (p.Ala390Val)	ENTPD6 (A353V +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365010	NM_001247.5(ENTPD6):c.1268C>T (p.Pro423Leu)	ENTPD6 (P386L +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3275552	NM_001247.5(ENTPD6):c.1375A>G (p.Asn459Asp)	ENTPD6 (N207D +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3089099	NM_001247.5(ENTPD6):c.1406T>C (p.Ile469Thr)	ENTPD6 (I435T +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 28