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

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2283884	NM_003236.4(TGFA):c.472A>C (p.Thr158Pro)	TGFA (T163P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537252	NM_003236.4(TGFA):c.455C>A (p.Ala152Asp)	TGFA (A152D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283883	NM_003236.4(TGFA):c.440T>A (p.Leu147Gln)	TGFA (L147Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325684	NM_003236.4(TGFA):c.433G>A (p.Ala145Thr)	TGFA (A144T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553262	NM_003236.4(TGFA):c.421G>A (p.Glu141Lys)	TGFA (E146K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176637	NM_003236.4(TGFA):c.406C>T (p.Leu136Phe)	TGFA (L142F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529765	NM_003236.4(TGFA):c.304G>A (p.Ala102Thr)	TGFA (A102T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176636	NM_003236.4(TGFA):c.232G>A (p.Val78Ile)	TGFA (V84I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176635	NM_003236.4(TGFA):c.128A>G (p.His43Arg)	TGFA (H42R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325683	NM_003236.4(TGFA):c.113C>A (p.Ala38Glu)	TGFA (A37E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226812	NM_003236.4(TGFA):c.86C>T (p.Pro29Leu)	TGFA (P29L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2374422	NM_003236.4(TGFA):c.11C>T (p.Ser4Leu)	TGFA (S4L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance