"Ambry Genetics"[submitter] AND "DCUN1D4"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2228078	NM_001040402.3(DCUN1D4):c.33G>C (p.Gln11His)	DCUN1D4 (Q11H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2221370	NM_001040402.3(DCUN1D4):c.47T>C (p.Leu16Pro)	DCUN1D4 (L16P +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2361776	NM_001040402.3(DCUN1D4):c.91A>G (p.Lys31Glu)	DCUN1D4 (K31E +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2214776	NM_001040402.3(DCUN1D4):c.112A>G (p.Ile38Val)	DCUN1D4 (I82V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2336988	NM_001040402.3(DCUN1D4):c.124G>A (p.Asp42Asn)	DCUN1D4 (D86N +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2278081	NM_001040402.3(DCUN1D4):c.341C>G (p.Ala114Gly)	DCUN1D4 (A114G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2301924	NM_001040402.3(DCUN1D4):c.396T>G (p.Ile132Met)	DCUN1D4 (I72M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232170	NM_001040402.3(DCUN1D4):c.439A>C (p.Lys147Gln)	DCUN1D4 (K147Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2256490	NM_001040402.3(DCUN1D4):c.472C>G (p.Leu158Val)	DCUN1D4 (L98V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2347810	NM_001040402.3(DCUN1D4):c.571A>G (p.Thr191Ala)	DCUN1D4 (T131A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2569833	NM_001040402.3(DCUN1D4):c.579T>A (p.Phe193Leu)	DCUN1D4 (F133L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance