Related gene-specific medical variations for Gene (Select 83666) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3273978	NM_138287.3(DTX3L):c.103T>C (p.Ser35Pro)	DTX3L, PARP9 (S35P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3086134	NM_138287.3(DTX3L):c.90C>A (p.Phe30Leu)	DTX3L, PARP9 (F30L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2491025	NM_138287.3(DTX3L):c.101A>C (p.Lys34Thr)	DTX3L, PARP9 (K34T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2306821	NM_138287.3(DTX3L):c.95G>C (p.Ser32Thr)	DTX3L, PARP9 (S32T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2284369	NM_138287.3(DTX3L):c.56G>A (p.Gly19Asp)	DTX3L, PARP9 (G19D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2272291	NM_138287.3(DTX3L):c.166G>T (p.Val56Leu)	DTX3L, PARP9 (V56L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 995677	NM_001146105.2(PARP9):c.1652T>C (p.Ile551Thr)	PARP9 (I551T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar