Related gene-specific medical variations for Gene (Select 26534) - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3302391	NM_001005466.2(OR10G2):c.211C>T (p.Leu71Phe)	OR10G2, TRA (L71F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302390	NM_001005466.2(OR10G2):c.661C>G (p.Leu221Val)	OR10G2, TRA (L221V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204506	NM_001005466.2(OR10G2):c.891C>A (p.Asn297Lys)	OR10G2, TRA (N297K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204505	NM_001005466.2(OR10G2):c.755T>C (p.Val252Ala)	OR10G2, TRA (V252A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204504	NM_001005466.2(OR10G2):c.74C>A (p.Pro25Gln)	OR10G2, TRA (P25Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204503	NM_001005466.2(OR10G2):c.698T>G (p.Ile233Arg)	OR10G2, TRA (I233R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204502	NM_001005466.2(OR10G2):c.586G>T (p.Asp196Tyr)	OR10G2, TRA (D196Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204501	NM_001005466.2(OR10G2):c.508C>T (p.Arg170Cys)	OR10G2, TRA (R170C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204500	NM_001005466.2(OR10G2):c.466G>A (p.Ala156Thr)	OR10G2, TRA (A156T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204499	NM_001005466.2(OR10G2):c.337G>A (p.Gly113Ser)	OR10G2, TRA (G113S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204498	NM_001005466.2(OR10G2):c.251C>T (p.Pro84Leu)	TRA, OR10G2 (P84L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204497	NM_001005466.2(OR10G2):c.131T>C (p.Leu44Pro)	OR10G2, TRA (L44P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608596	NM_001005466.2(OR10G2):c.274C>T (p.Pro92Ser)	OR10G2, TRA (P92S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606175	NM_001005466.2(OR10G2):c.109A>G (p.Ile37Val)	OR10G2, TRA (I37V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2534966	NM_001005466.2(OR10G2):c.667T>C (p.Tyr223His)	OR10G2, TRA (Y223H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473746	NM_001005466.2(OR10G2):c.79C>A (p.Leu27Ile)	OR10G2, TRA (L27I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466900	NM_001005466.2(OR10G2):c.44A>C (p.Asp15Ala)	OR10G2, TRA (D15A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387796	NM_001005466.2(OR10G2):c.722G>A (p.Arg241Gln)	OR10G2, TRA (R241Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377686	NM_001005466.2(OR10G2):c.245C>T (p.Thr82Ile)	OR10G2, TRA (T82I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2359499	NM_001005466.2(OR10G2):c.15A>T (p.Lys5Asn)	OR10G2, TRA (K5N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349397	NM_001005466.2(OR10G2):c.668A>G (p.Tyr223Cys)	OR10G2, TRA (Y223C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338106	NM_001005466.2(OR10G2):c.184C>T (p.Arg62Cys)	OR10G2, TRA (R62C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330851	NM_001005466.2(OR10G2):c.911T>C (p.Leu304Pro)	OR10G2, TRA (L304P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321454	NM_001005466.2(OR10G2):c.290T>C (p.Ile97Thr)	OR10G2, TRA (I97T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316582	NM_001005466.2(OR10G2):c.41C>G (p.Thr14Arg)	OR10G2, TRA (T14R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299444	NM_001005466.2(OR10G2):c.469G>A (p.Gly157Ser)	OR10G2, TRA (G157S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297449	NM_001005466.2(OR10G2):c.23C>T (p.Ser8Leu)	OR10G2, TRA (S8L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241084	NM_001005466.2(OR10G2):c.577G>T (p.Ala193Ser)	OR10G2, TRA (A193S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212508	NM_001005466.2(OR10G2):c.34G>A (p.Val12Met)	OR10G2, TRA (V12M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207461	NM_001005466.2(OR10G2):c.119T>A (p.Ile40Asn)	OR10G2, TRA (I40N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 30