"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "TGFB3"[gene] - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 191778	NM_003239.5(TGFB3):c.559G>A (p.Gly187Ser)	TGFB3 (G187S)	Single nucleotide variant (missense variant)	Rienhoff syndrome +3 more	GUncertain significance
Select item 1394740	NM_003239.5(TGFB3):c.230G>A (p.Arg77Gln)	TGFB3 (R77Q)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 2683270	NM_003239.5(TGFB3):c.43C>A (p.Leu15Met)	TGFB3 (L15M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

Format

Sort by

Choose Destination

ClinVar