Related gene-specific medical variations for Gene (Select 26659) - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3303381	NM_017506.2(OR7A5):c.805C>T (p.His269Tyr)	OR7A5, OR7C1 (H269Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3206632	NM_017506.2(OR7A5):c.758G>A (p.Gly253Asp)	OR7A5, OR7C1 (G253D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3206631	NM_017506.2(OR7A5):c.742G>C (p.Val248Leu)	OR7A5, OR7C1 (V248L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3206630	NM_017506.2(OR7A5):c.608T>C (p.Val203Ala)	OR7A5, OR7C1 (V203A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2622158	NM_017506.2(OR7A5):c.680C>T (p.Ala227Val)	OR7A5, OR7C1 (A227V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615044	NM_017506.2(OR7A5):c.305A>G (p.Tyr102Cys)	OR7A5, OR7C1 (Y102C)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2602315	NM_017506.2(OR7A5):c.275T>C (p.Ile92Thr)	OR7A5, OR7C1 (I92T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590986	NM_017506.2(OR7A5):c.365G>A (p.Arg122Gln)	OR7A5, OR7C1 (R122Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518646	NM_017506.2(OR7A5):c.796C>T (p.Arg266Cys)	OR7A5, OR7C1 (R266C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518125	NM_017506.2(OR7A5):c.83T>C (p.Phe28Ser)	OR7A5, OR7C1 (F28S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511165	NM_017506.2(OR7A5):c.776A>G (p.Tyr259Cys)	OR7A5, OR7C1 (Y259C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466455	NM_017506.2(OR7A5):c.406A>G (p.Met136Val)	OR7A5, OR7C1 (M136V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394306	NM_017506.2(OR7A5):c.494G>A (p.Arg165Gln)	OR7A5, OR7C1 (R165Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370077	NM_017506.2(OR7A5):c.622G>A (p.Gly208Arg)	OR7A5, OR7C1 (G208R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349674	NM_017506.2(OR7A5):c.734T>G (p.Leu245Arg)	OR7A5, OR7C1 (L245R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345064	NM_017506.2(OR7A5):c.845C>G (p.Thr282Ser)	OR7A5, OR7C1 (T282S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344716	NM_017506.2(OR7A5):c.652T>C (p.Tyr218His)	OR7A5, OR7C1 (Y218H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333701	NM_017506.2(OR7A5):c.355G>A (p.Ala119Thr)	OR7A5, OR7C1 (A119T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2285324	NM_017506.2(OR7A5):c.635C>G (p.Thr212Ser)	OR7A5, OR7C1 (T212S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278392	NM_017506.2(OR7A5):c.167A>C (p.His56Pro)	OR7A5, OR7C1 (H56P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258245	NM_017506.2(OR7A5):c.215G>T (p.Cys72Phe)	OR7A5, OR7C1 (C72F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242449	NM_017506.2(OR7A5):c.597A>G (p.Ile199Met)	OR7A5, OR7C1 (I199M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2215376	NM_017506.2(OR7A5):c.130C>A (p.Leu44Ile)	OR7A5, OR7C1 (L44I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208438	NM_017506.2(OR7A5):c.910C>T (p.His304Tyr)	OR7A5, OR7C1 (H304Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204913	NM_017506.2(OR7A5):c.62C>G (p.Pro21Arg)	OR7A5, OR7C1 (P21R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 25