ClinVar (all) for Orgtrack (Select 500114) - ClinVar

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

Format

Sort by

Choose Destination

Links from Orgtrack

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 91860	NM_005762.3(TRIM28):c.1216+23C>T	TRIM28	Single nucleotide variant (intron variant)	Familial colorectal cancer	Gnot provided
Select item 55934	NM_182710.3(KAT5):c.638T>G (p.Val213Gly)	KAT5 (V213G +3 more)	Single nucleotide variant (missense variant)	Familial colorectal cancer	Gnot provided