OR14A16[gene] and "single gene"[properties] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2278984	NM_001001966.2(OR14A16):c.920C>A (p.Thr307Asn)	OR14A16 (T307N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302527	NM_001001966.2(OR14A16):c.863G>A (p.Ser288Asn)	OR14A16 (S288N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545630	NM_001001966.2(OR14A16):c.841A>T (p.Thr281Ser)	OR14A16 (T281S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539638	NM_001001966.2(OR14A16):c.800T>G (p.Leu267Trp)	OR14A16 (L267W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557557	NM_001001966.2(OR14A16):c.791C>T (p.Pro264Leu)	OR14A16 (P264L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290352	NM_001001966.2(OR14A16):c.784G>C (p.Glu262Gln)	OR14A16 (E262Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370875	NM_001001966.2(OR14A16):c.761T>C (p.Ile254Thr)	OR14A16 (I254T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204826	NM_001001966.2(OR14A16):c.757T>A (p.Phe253Ile)	OR14A16 (F253I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396838	NM_001001966.2(OR14A16):c.726C>A (p.His242Gln)	OR14A16 (H242Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204825	NM_001001966.2(OR14A16):c.632T>G (p.Val211Gly)	OR14A16 (V211G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233550	NM_001001966.2(OR14A16):c.604G>A (p.Val202Ile)	OR14A16 (V202I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357151	NM_001001966.2(OR14A16):c.596T>A (p.Leu199His)	OR14A16 (L199H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250550	NM_001001966.2(OR14A16):c.574A>G (p.Ile192Val)	OR14A16 (I192V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204824	NM_001001966.2(OR14A16):c.521A>G (p.Gln174Arg)	OR14A16 (Q174R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204823	NM_001001966.2(OR14A16):c.482C>A (p.Thr161Asn)	OR14A16 (T161N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204820	NM_001001966.2(OR14A16):c.470A>T (p.His157Leu)	OR14A16 (H157L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161477	NM_001001966.2(OR14A16):c.341C>T (p.Thr114Met)	OR14A16 (T114M)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 3302528	NM_001001966.2(OR14A16):c.280G>A (p.Gly94Ser)	OR14A16 (G94S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204819	NM_001001966.2(OR14A16):c.252G>C (p.Leu84Phe)	OR14A16 (L84F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204817	NM_001001966.2(OR14A16):c.187A>C (p.Asn63His)	OR14A16 (N63H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256347	NM_001001966.2(OR14A16):c.169G>A (p.Val57Met)	OR14A16 (V57M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204816	NM_001001966.2(OR14A16):c.147G>C (p.Leu49Phe)	OR14A16 (L49F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204815	NM_001001966.2(OR14A16):c.131T>C (p.Ile44Thr)	OR14A16 (I44T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302526	NM_001001966.2(OR14A16):c.130A>G (p.Ile44Val)	OR14A16 (I44V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536481	NM_001001966.2(OR14A16):c.112A>G (p.Met38Val)	OR14A16 (M38V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291443	NM_001001966.2(OR14A16):c.43T>A (p.Phe15Ile)	OR14A16 (F15I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204818	NM_001001966.2(OR14A16):c.19G>A (p.Val7Met)	OR14A16 (V7M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 27