AQP9[gene] and "single gene"[properties] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2387820	NM_020980.5(AQP9):c.77C>A (p.Thr26Asn)	AQP9 (T26N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309197	NM_020980.5(AQP9):c.149G>T (p.Ser50Ile)	AQP9 (S50I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351357	NM_020980.5(AQP9):c.158G>A (p.Arg53His)	AQP9 (R53H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3128155	NM_020980.5(AQP9):c.214A>G (p.Ile72Val)	AQP9 (I7V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254837	NM_020980.5(AQP9):c.229G>T (p.Gly77Cys)	AQP9 (G77C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3128156	NM_020980.5(AQP9):c.296G>T (p.Trp99Leu)	AQP9 (W34L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2645380	NM_020980.5(AQP9):c.357C>T (p.Thr119=)	AQP9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3128157	NM_020980.5(AQP9):c.358G>A (p.Val120Ile)	AQP9 (V120I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309208	NM_020980.5(AQP9):c.377A>G (p.Asp126Gly)	AQP9 (D126G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299865	NM_020980.5(AQP9):c.415G>A (p.Val139Met)	AQP9 (V74M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218555	NM_020980.5(AQP9):c.455C>G (p.Pro152Arg)	AQP9 (P87R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285849	NM_020980.5(AQP9):c.457G>A (p.Ala153Thr)	AQP9 (A153T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309185	NM_020980.5(AQP9):c.461C>T (p.Pro154Leu)	AQP9 (P154L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390980	NM_020980.5(AQP9):c.476C>T (p.Ala159Val)	AQP9 (A159V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3128158	NM_020980.5(AQP9):c.555G>T (p.Leu185Phe)	AQP9 (L185F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596860	NM_020980.5(AQP9):c.587T>G (p.Ile196Ser)	AQP9 (I131S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483191	NM_020980.5(AQP9):c.587T>C (p.Ile196Thr)	AQP9 (I196T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2375713	NM_020980.5(AQP9):c.604G>A (p.Val202Ile)	AQP9 (V137I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619836	NM_020980.5(AQP9):c.626T>G (p.Leu209Arg)	AQP9 (L209R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308174	NM_020980.5(AQP9):c.764C>T (p.Ala255Val)	AQP9 (A255V +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3309218	NM_020980.5(AQP9):c.770T>C (p.Ile257Thr)	AQP9 (I192T +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2532042	NM_020980.5(AQP9):c.829T>C (p.Phe277Leu)	AQP9 (F212L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3128159	NM_020980.5(AQP9):c.871C>T (p.Leu291Phe)	AQP9 (L291F +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 23