"Ambry Genetics"[submitter] AND "IGFL4"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2486848	NM_001002923.3(IGFL4):c.347G>T (p.Ser116Ile)	IGFL4 (S116I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2613306	NM_001002923.3(IGFL4):c.337C>A (p.His113Asn)	IGFL4 (H113N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2206946	NM_001002923.3(IGFL4):c.307C>T (p.Pro103Ser)	IGFL4 (P103S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2375864	NM_001002923.3(IGFL4):c.271A>G (p.Lys91Glu)	IGFL4 (K91E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2241078	NM_001002923.3(IGFL4):c.187G>A (p.Gly63Ser)	IGFL4 (G63S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2525091	NM_001002923.3(IGFL4):c.178C>T (p.Arg60Trp)	IGFL4 (R60W)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2205851	NM_001002923.3(IGFL4):c.140G>A (p.Cys47Tyr)	IGFL4 (C47Y)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2553984	NM_001002923.3(IGFL4):c.130T>G (p.Leu44Val)	IGFL4 (L44V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance