Related gene-specific medical variations for Gene (Select 11236) - ClinVar

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

Format

Sort by

Choose Destination

Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2615923	NM_032026.4(TATDN1):c.886G>A (p.Gly296Arg)	RNF139, TATDN1 (G151R +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2386533	NM_032026.4(TATDN1):c.878T>C (p.Phe293Ser)	RNF139, TATDN1 (F329S +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance