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

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2261801	NM_012336.4(NARF):c.19A>C (p.Thr7Pro)	NARF (T7P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2264319	NM_012336.4(NARF):c.54T>A (p.Asp18Glu)	NARF (D18E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2622757	NM_012336.4(NARF):c.91G>C (p.Ala31Pro)	NARF (A31P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2411190	NM_012336.4(NARF):c.106G>A (p.Glu36Lys)	NARF (E36K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2464806	NM_012336.4(NARF):c.206C>G (p.Ser69Cys)	NARF (S69C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392287	NM_012336.4(NARF):c.235G>A (p.Val79Ile)	NARF (V20I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3298443	NM_012336.4(NARF):c.260A>G (p.Asp87Gly)	NARF (D28G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298439	NM_012336.4(NARF):c.410C>T (p.Thr137Met)	NARF (T137M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513130	NM_012336.4(NARF):c.419C>T (p.Ala140Val)	NARF (A140V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508466	NM_012336.4(NARF):c.454G>C (p.Val152Leu)	NARF (V104L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409299	NM_012336.4(NARF):c.466C>T (p.Arg156Cys)	NARF (R156C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394943	NM_012336.4(NARF):c.467G>A (p.Arg156His)	NARF (R108H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2544986	NM_012336.4(NARF):c.487C>A (p.Arg163Ser)	NARF (R163S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465036	NM_012336.4(NARF):c.487C>T (p.Arg163Cys)	NARF (R104C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535350	NM_012336.4(NARF):c.502C>G (p.Leu168Val)	NARF (L109V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460597	NM_012336.4(NARF):c.554G>A (p.Arg185His)	NARF (R137H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3175571	NM_012336.4(NARF):c.580G>A (p.Ala194Thr)	NARF (A135T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383411	NM_012336.4(NARF):c.628G>A (p.Ala210Thr)	NARF (A151T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298438	NM_012336.4(NARF):c.680C>T (p.Pro227Leu)	NARF (P168L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394265	NM_012336.4(NARF):c.743G>A (p.Arg248Gln)	NARF (R200Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308480	NM_012336.4(NARF):c.755G>A (p.Cys252Tyr)	NARF (C193Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298444	NM_012336.4(NARF):c.770G>T (p.Gly257Val)	NARF (G209V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370017	NM_012336.4(NARF):c.809T>A (p.Val270Glu)	NARF (V316E +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3298440	NM_012336.4(NARF):c.823G>A (p.Val275Ile)	NARF (V227I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175588	NM_012336.4(NARF):c.826G>C (p.Asp276His)	NARF (D322H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175508	NM_012336.4(NARF):c.866G>A (p.Arg289His)	NARF (R230H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467653	NM_012336.4(NARF):c.962G>A (p.Arg321Gln)	NARF (R262Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353664	NM_012336.4(NARF):c.1040A>G (p.Tyr347Cys)	NARF (Y347C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359497	NM_012336.4(NARF):c.1054A>C (p.Ile352Leu)	NARF (I293L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239359	NM_012336.4(NARF):c.1114C>T (p.Leu372Phe)	NARF (L324F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175524	NM_012336.4(NARF):c.1175C>T (p.Ala392Val)	NARF (A333V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298441	NM_012336.4(NARF):c.1207A>G (p.Ile403Val)	NARF (I403V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359470	NM_012336.4(NARF):c.1229G>A (p.Arg410Gln)	NARF (R362Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272666	NM_012336.4(NARF):c.1231C>T (p.Arg411Cys)	NARF (R363C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361602	NM_012336.4(NARF):c.1235C>T (p.Pro412Leu)	NARF (P353L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538911	NM_012336.4(NARF):c.1285A>C (p.Ile429Leu)	NARF (I370L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527153	NM_012336.4(NARF):c.1289A>G (p.Asn430Ser)	NARF (N371S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270394	NM_012336.4(NARF):c.1292C>T (p.Ser431Phe)	NARF (S383F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 38