Related gene-specific medical variations for Gene (Select 1854) - 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 3068241	NM_001025248.2(DUT):c.647G>A (p.Arg216Gln)	DUT (R105Q +3 more)	Single nucleotide variant (missense variant)	Bone marrow failure and diabetes mellitus syndrome	GUncertain significance
Select item 2245952	NM_001025248.2(DUT):c.158T>C (p.Ile53Thr)	DUT, DUT-AS1 +1 more (I53T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 1336417	NM_001025248.2(DUT):c.280+9G>A	DUT, DUT-AS1 +1 more	Single nucleotide variant (intron variant)	not specified	GBenign

Format

Sort by

Choose Destination