Related gene-specific medical variations for Gene (Select 125958) - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3303392	NM_001005191.3(OR7D4):c.487A>G (p.Met163Val)	OR7D4, OR7E24 (M163V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3303391	NM_001005191.3(OR7D4):c.785C>T (p.Ser262Phe)	OR7D4, OR7E24 (S262F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3303390	NM_001005191.3(OR7D4):c.540A>T (p.Glu180Asp)	OR7D4, OR7E24 (E180D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3303389	NM_001005191.3(OR7D4):c.479T>G (p.Ile160Ser)	OR7D4, OR7E24 (I160S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206656	NM_001005191.3(OR7D4):c.817A>T (p.Thr273Ser)	OR7D4, OR7E24 (T273S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206655	NM_001005191.3(OR7D4):c.653A>C (p.Tyr218Ser)	OR7D4, OR7E24 (Y218S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206654	NM_001005191.3(OR7D4):c.431T>C (p.Leu144Pro)	OR7D4, OR7E24 (L144P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206653	NM_001005191.3(OR7D4):c.354G>A (p.Met118Ile)	OR7D4, OR7E24 (M118I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206652	NM_001005191.3(OR7D4):c.223T>A (p.Ser75Thr)	OR7D4, OR7E24 (S75T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206651	NM_001005191.3(OR7D4):c.188T>A (p.Leu63His)	OR7D4, OR7E24 (L63H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206650	NM_001005191.3(OR7D4):c.14A>C (p.Asn5Thr)	OR7D4, OR7E24 (N5T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552381	NM_001005191.3(OR7D4):c.847C>G (p.Pro283Ala)	OR7D4, OR7E24 (P283A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526037	NM_001005191.3(OR7D4):c.511G>A (p.Gly171Ser)	OR7D4, OR7E24 (G171S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467844	NM_001005191.3(OR7D4):c.803C>T (p.Ser268Phe)	OR7D4, OR7E24 (S268F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454666	NM_001005191.3(OR7D4):c.418C>T (p.Leu140Phe)	OR7D4, OR7E24 (L140F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409571	NM_001005191.3(OR7D4):c.328A>G (p.Met110Val)	OR7D4, OR7E24 (M110V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392887	NM_001005191.3(OR7D4):c.718A>C (p.Thr240Pro)	OR7D4, OR7E24 (T240P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381850	NM_001005191.3(OR7D4):c.598T>A (p.Tyr200Asn)	OR7D4, OR7E24 (Y200N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375961	NM_001005191.3(OR7D4):c.925G>A (p.Asp309Asn)	OR7D4, OR7E24 (D309N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371044	NM_001005191.3(OR7D4):c.617T>A (p.Leu206Gln)	OR7D4, OR7E24 (L206Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344898	NM_001005191.3(OR7D4):c.170C>G (p.Thr57Ser)	OR7D4, OR7E24 (T57S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280958	NM_001005191.3(OR7D4):c.909A>T (p.Arg303Ser)	OR7D4, OR7E24 (R303S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270707	NM_001005191.3(OR7D4):c.247G>A (p.Val83Met)	OR7D4, OR7E24 (V83M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239993	NM_001005191.3(OR7D4):c.224C>G (p.Ser75Cys)	OR7D4, OR7E24 (S75C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205325	NM_001005191.3(OR7D4):c.95T>C (p.Leu32Pro)	OR7E24, OR7D4 (L32P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777413	NM_001005191.3(OR7D4):c.496T>C (p.Leu166=)	OR7D4, OR7E24	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 777412	NM_001005191.3(OR7D4):c.924C>T (p.Ala308=)	OR7D4, OR7E24	Single nucleotide variant (synonymous variant)	not provided	GBenign

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Links from Gene

Items: 27