"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "NODAL"[gen - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 95883	NM_018055.5(NODAL):c.904C>T (p.Arg302Cys)	NODAL (R302C +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1335040	NM_018055.5(NODAL):c.285G>C (p.Leu95=)	NODAL	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 473049	NM_018055.5(NODAL):c.9C>T (p.Ala3=)	NODAL	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign

Format

Sort by

Choose Destination

ClinVar