"PreventionGenetics, part of Exact Sciences"[submitter] AND "ULK4"[gen - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040202	NM_017886.4(ULK4):c.3250C>T (p.Leu1084=)	ULK4	Single nucleotide variant (synonymous variant +1 more)	ULK4-related disorder	GLikely benign
Select item 224080	NM_017886.4(ULK4):c.2887G>A (p.Val963Met)	ULK4 (V963M +1 more)	Single nucleotide variant (missense variant +1 more)	ULK4-related disorder +1 more	GLikely benign
Select item 3048584	NM_017886.4(ULK4):c.2849T>C (p.Phe950Ser)	ULK4 (F648S +1 more)	Single nucleotide variant (missense variant +1 more)	ULK4-related disorder	GLikely benign
Select item 3053027	NM_017886.4(ULK4):c.2649T>C (p.Ser883=)	ULK4	Single nucleotide variant (synonymous variant +1 more)	ULK4-related disorder	GLikely benign
Select item 224081	NM_017886.4(ULK4):c.2584C>T (p.Arg862Ter)	ULK4 (R862* +1 more)	Single nucleotide variant (nonsense +1 more)	ULK4-related disorder +1 more	GLikely benign
Select item 3060808	NM_017886.4(ULK4):c.2551G>A (p.Val851Ile)	ULK4 (V549I +1 more)	Single nucleotide variant (missense variant +1 more)	ULK4-related disorder	GBenign
Select item 3035347	NM_017886.4(ULK4):c.2541C>T (p.Pro847=)	ULK4	Single nucleotide variant (synonymous variant +1 more)	ULK4-related disorder	GLikely benign
Select item 3059926	NM_017886.4(ULK4):c.2530T>A (p.Leu844Met)	ULK4 (L542M +1 more)	Single nucleotide variant (missense variant +1 more)	ULK4-related disorder	GBenign
Select item 3043434	NM_017886.4(ULK4):c.2388T>C (p.Asn796=)	ULK4	Single nucleotide variant (synonymous variant +1 more)	ULK4-related disorder	GLikely benign
Select item 2221044	NM_017886.4(ULK4):c.2272T>C (p.Tyr758His)	ULK4 (Y758H +1 more)	Single nucleotide variant (missense variant +1 more)	ULK4-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 2653697	NM_017886.4(ULK4):c.2217T>C (p.Arg739=)	ULK4	Single nucleotide variant (synonymous variant +1 more)	ULK4-related disorder +1 more	GLikely benign
Select item 3058955	NM_017886.4(ULK4):c.2143G>A (p.Ala715Thr)	ULK4 (A413T +1 more)	Single nucleotide variant (missense variant +1 more)	ULK4-related disorder	GBenign
Select item 224082	NM_017886.4(ULK4):c.2056G>A (p.Val686Ile)	ULK4 (V686I +1 more)	Single nucleotide variant (missense variant +1 more)	ULK4-related disorder +2 more	GLikely benign
Select item 3038191	NM_017886.4(ULK4):c.1808T>C (p.Leu603Ser)	ULK4 (L301S +1 more)	Single nucleotide variant (missense variant +1 more)	ULK4-related disorder	GBenign
Select item 3060720	NM_017886.4(ULK4):c.1764+3G>A	ULK4	Single nucleotide variant (intron variant)	ULK4-related disorder	GLikely benign
Select item 3058867	NM_017886.4(ULK4):c.1706A>G (p.Lys569Arg)	ULK4 (K267R +1 more)	Single nucleotide variant (missense variant +1 more)	ULK4-related disorder	GBenign
Select item 787013	NM_017886.4(ULK4):c.1626T>C (p.Ala542=)	ULK4	Single nucleotide variant (synonymous variant +1 more)	ULK4-related disorder +1 more	GBenign/Likely benign
Select item 3051002	NM_017886.4(ULK4):c.1160A>G (p.Gln387Arg)	ULK4 (Q387R +1 more)	Single nucleotide variant (missense variant +1 more)	ULK4-related disorder	GLikely benign
Select item 3055633	NM_017886.4(ULK4):c.1056T>C (p.Gly352=)	ULK4	Single nucleotide variant (synonymous variant)	ULK4-related disorder	GBenign
Select item 3059632	NM_017886.4(ULK4):c.1042A>G (p.Ser348Gly)	ULK4 (S348G +1 more)	Single nucleotide variant (missense variant)	ULK4-related disorder	GBenign
Select item 3052241	NM_017886.4(ULK4):c.896+5T>G	ULK4	Single nucleotide variant (intron variant)	ULK4-related disorder	GLikely benign
Select item 3041376	NM_017886.4(ULK4):c.876C>T (p.Ser292=)	ULK4	Single nucleotide variant (synonymous variant +2 more)	ULK4-related disorder	GLikely benign
Select item 2653699	NM_017886.4(ULK4):c.493G>A (p.Asp165Asn)	ULK4 (D165N)	Single nucleotide variant (missense variant +2 more)	ULK4-related disorder +1 more	GLikely benign
Select item 3056778	NM_017886.4(ULK4):c.165C>T (p.His55=)	ULK4	Single nucleotide variant (synonymous variant +2 more)	ULK4-related disorder	GLikely benign

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Items: 24