C0238463[trait identifier] AND "St. Jude Molecular Pathology, St. Jude - ClinVar

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

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 620632	NM_206937.2(LIG4):c.1673A>C (p.Gln558Pro)	LIG4 (Q558P +2 more)	Single nucleotide variant (missense variant)	Papillary thyroid carcinoma	GLikely pathogenic
Select item 232654	NM_024675.4(PALB2):c.2147A>G (p.Asn716Ser)	PALB2 (N716S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GUncertain significance