"Ambry Genetics"[submitter] AND "ANGPTL1"[gene] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2270737	NM_004673.4(ANGPTL1):c.1469T>A (p.Ile490Asn)	ANGPTL1, RALGPS2 (I490N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314859	NM_004673.4(ANGPTL1):c.1457T>C (p.Met486Thr)	ANGPTL1, RALGPS2 (M486T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118442	NM_004673.4(ANGPTL1):c.1426G>A (p.Gly476Arg)	ANGPTL1, RALGPS2 (G476R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301999	NM_004673.4(ANGPTL1):c.1406T>G (p.Phe469Cys)	ANGPTL1, RALGPS2 (F469C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2315613	NM_004673.4(ANGPTL1):c.1309A>G (p.Lys437Glu)	ANGPTL1, RALGPS2 (K437E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493838	NM_004673.4(ANGPTL1):c.1294T>C (p.Cys432Arg)	ANGPTL1, RALGPS2 (C432R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309238	NM_004673.4(ANGPTL1):c.1261C>G (p.Leu421Val)	ANGPTL1, RALGPS2 (L421V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118424	NM_004673.4(ANGPTL1):c.1224T>A (p.Asp408Glu)	ANGPTL1, RALGPS2 (D408E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288930	NM_004673.4(ANGPTL1):c.1210G>A (p.Gly404Arg)	ANGPTL1, RALGPS2 (G404R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472330	NM_004673.4(ANGPTL1):c.1193G>A (p.Arg398His)	ANGPTL1, RALGPS2 (R398H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118411	NM_004673.4(ANGPTL1):c.1159C>T (p.Arg387Cys)	ANGPTL1, RALGPS2 (R387C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118406	NM_004673.4(ANGPTL1):c.1154G>C (p.Ser385Thr)	ANGPTL1, RALGPS2 (S385T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118404	NM_004673.4(ANGPTL1):c.1013A>G (p.Tyr338Cys)	ANGPTL1, RALGPS2 (Y338C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404539	NM_004673.4(ANGPTL1):c.976G>C (p.Asp326His)	ANGPTL1, RALGPS2 (D326H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402444	NM_004673.4(ANGPTL1):c.966G>C (p.Gln322His)	ANGPTL1, RALGPS2 (Q322H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490838	NM_004673.4(ANGPTL1):c.907G>A (p.Gly303Arg)	ANGPTL1, RALGPS2 (G303R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118508	NM_004673.4(ANGPTL1):c.904A>C (p.Asn302His)	ANGPTL1, RALGPS2 (N302H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118500	NM_004673.4(ANGPTL1):c.866C>T (p.Ser289Leu)	ANGPTL1, RALGPS2 (S289L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267669	NM_004673.4(ANGPTL1):c.866C>G (p.Ser289Trp)	ANGPTL1, RALGPS2 (S289W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208785	NM_004673.4(ANGPTL1):c.839G>A (p.Cys280Tyr)	ANGPTL1, RALGPS2 (C280Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118490	NM_004673.4(ANGPTL1):c.813C>G (p.Phe271Leu)	ANGPTL1, RALGPS2 (F271L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244509	NM_004673.4(ANGPTL1):c.794A>G (p.Lys265Arg)	ANGPTL1, RALGPS2 (K265R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118479	NM_004673.4(ANGPTL1):c.763C>G (p.Leu255Val)	ANGPTL1, RALGPS2 (L255V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118474	NM_004673.4(ANGPTL1):c.730G>A (p.Gly244Ser)	ANGPTL1, RALGPS2 (G244S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385302	NM_004673.4(ANGPTL1):c.641C>A (p.Pro214Gln)	ANGPTL1, RALGPS2 (P214Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261054	NM_004673.4(ANGPTL1):c.607A>G (p.Ile203Val)	ANGPTL1, RALGPS2 (I203V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118460	NM_004673.4(ANGPTL1):c.491A>C (p.Glu164Ala)	ANGPTL1, RALGPS2 (E164A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350981	NM_004673.4(ANGPTL1):c.479A>G (p.Asn160Ser)	ANGPTL1, RALGPS2 (N160S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118454	NM_004673.4(ANGPTL1):c.296T>C (p.Ile99Thr)	ANGPTL1, RALGPS2 (I99T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118449	NM_004673.4(ANGPTL1):c.289C>T (p.Arg97Trp)	ANGPTL1, RALGPS2 (R97W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542211	NM_004673.4(ANGPTL1):c.84T>G (p.Ile28Met)	ANGPTL1, RALGPS2 (I28M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118481	NM_004673.4(ANGPTL1):c.76T>C (p.Phe26Leu)	ANGPTL1, RALGPS2 (F26L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373598	NM_004673.4(ANGPTL1):c.11T>C (p.Phe4Ser)	ANGPTL1, RALGPS2 (F4S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 33