Related gene-specific medical variations for Gene (Select 84294) - 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 3331743	NM_032334.3(UTP23):c.36T>G (p.His12Gln)	LOC130000991, UTP23 (H12Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552471	NM_032334.3(UTP23):c.8T>A (p.Ile3Asn)	LOC130000991, UTP23 (I3N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361479	NM_032334.3(UTP23):c.161T>G (p.Met54Arg)	LOC130000991, UTP23 (M54R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

Format

Sort by

Choose Destination