"Ambry Genetics"[submitter] AND "ULK3"[gene] - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2479642	NM_001099436.4(ULK3):c.1385C>T (p.Ser462Leu)	ULK3 (S473L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338179	NM_001099436.4(ULK3):c.1349G>A (p.Arg450His)	ULK3 (R333H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2298274	NM_001099436.4(ULK3):c.1336A>G (p.Met446Val)	ULK3 (M329V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186359	NM_001099436.4(ULK3):c.1333A>G (p.Lys445Glu)	ULK3 (K445E +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2597395	NM_001099436.4(ULK3):c.1268G>A (p.Arg423Gln)	ULK3 (R434Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186358	NM_001099436.4(ULK3):c.1252C>T (p.Pro418Ser)	ULK3 (P429S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2315239	NM_001099436.4(ULK3):c.1251G>T (p.Glu417Asp)	ULK3 (E417D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312117	NM_001099436.4(ULK3):c.1196C>T (p.Ala399Val)	ULK3 (A282V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490627	NM_001099436.4(ULK3):c.1082C>T (p.Ser361Phe)	ULK3 (S244F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599343	NM_001099436.4(ULK3):c.1067T>G (p.Leu356Arg)	ULK3 (L239R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294065	NM_001099436.4(ULK3):c.1054A>C (p.Asn352His)	ULK3 (N235H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622474	NM_001099436.4(ULK3):c.1024G>A (p.Glu342Lys)	ULK3 (E342K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559738	NM_001099436.4(ULK3):c.1018C>T (p.Arg340Trp)	ULK3 (R351W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186367	NM_001099436.4(ULK3):c.895G>T (p.Asp299Tyr)	ULK3 (D310Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244726	NM_001099436.4(ULK3):c.857C>T (p.Ala286Val)	ULK3 (A169V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204895	NM_001099436.4(ULK3):c.845G>A (p.Gly282Glu)	ULK3 (G282E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2268046	NM_001099436.4(ULK3):c.820C>A (p.His274Asn)	ULK3 (H157N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531262	NM_001099436.4(ULK3):c.785A>G (p.Gln262Arg)	ULK3 (Q262R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597019	NM_001099436.4(ULK3):c.769C>T (p.Arg257Cys)	ULK3 (R140C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207303	NM_001099436.4(ULK3):c.731G>A (p.Arg244Gln)	ULK3 (R255Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186364	NM_001099436.4(ULK3):c.706C>G (p.Arg236Gly)	ULK3 (R119G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186363	NM_001099436.4(ULK3):c.688G>A (p.Val230Ile)	ULK3 (V230I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519285	NM_001099436.4(ULK3):c.669G>C (p.Glu223Asp)	ULK3 (E223D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549553	NM_001099436.4(ULK3):c.656C>T (p.Ser219Leu)	ULK3 (S230L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3186361	NM_001099436.4(ULK3):c.577C>T (p.Arg193Cys)	ULK3 (R204C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2552769	NM_001099436.4(ULK3):c.574G>A (p.Ala192Thr)	ULK3 (A192T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488284	NM_001099436.4(ULK3):c.532C>G (p.Leu178Val)	ULK3 (L178V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532911	NM_001099436.4(ULK3):c.343C>T (p.Arg115Cys)	ULK3 (R115C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3186360	NM_001099436.4(ULK3):c.341C>T (p.Ala114Val)	ULK3 (A125V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2589990	NM_001099436.4(ULK3):c.257A>G (p.Asn86Ser)	ULK3 (N97S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2528136	NM_001099436.4(ULK3):c.251G>A (p.Ser84Asn)	ULK3 (S95N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3186365	NM_001099436.4(ULK3):c.80C>T (p.Thr27Met)	ULK3 (T27M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2261791	NM_001099436.4(ULK3):c.76G>A (p.Ala26Thr)	ULK3 (A26T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2228722	NM_001099436.4(ULK3):c.23C>T (p.Pro8Leu)	ULK3 (P8L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2407267	NM_001099436.4(ULK3):c.22C>T (p.Pro8Ser)	ULK3 (P8S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2312118	NM_001099436.4(ULK3):c.20G>A (p.Gly7Asp)	ULK3 (G7D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 36