AQP10[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2216891	NM_080429.3(AQP10):c.20C>T (p.Pro7Leu)	AQP10 (P7L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3128105	NM_080429.3(AQP10):c.50G>A (p.Arg17His)	AQP10 (R17H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777751	NM_080429.3(AQP10):c.105+10A>G	AQP10	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2344640	NM_080429.3(AQP10):c.139A>G (p.Thr47Ala)	AQP10 (T47A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508152	NM_080429.3(AQP10):c.385T>A (p.Tyr129Asn)	AQP10 (Y129N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3128106	NM_080429.3(AQP10):c.542G>A (p.Arg181Gln)	AQP10 (R181Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602144	NM_080429.3(AQP10):c.628G>A (p.Gly210Arg)	AQP10 (G210R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487355	NM_080429.3(AQP10):c.642C>A (p.Asn214Lys)	AQP10 (N214K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284764	NM_080429.3(AQP10):c.887T>C (p.Met296Thr)	AQP10 (M296T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar