GPR153[gene] and "single gene"[properties] - ClinVar

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Items: 80

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3101510	NM_207370.4(GPR153):c.1766G>C (p.Ser589Thr)	GPR153 (S589T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593675	NM_207370.4(GPR153):c.1751C>G (p.Thr584Ser)	GPR153 (T584S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229578	NM_207370.4(GPR153):c.1738G>A (p.Gly580Ser)	GPR153 (G580S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229348	NM_207370.4(GPR153):c.1736G>C (p.Gly579Ala)	GPR153 (G579A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209646	NM_207370.4(GPR153):c.1718G>A (p.Gly573Glu)	GPR153 (G573E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522600	NM_207370.4(GPR153):c.1699G>A (p.Ala567Thr)	GPR153 (A567T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300256	NM_207370.4(GPR153):c.1697G>C (p.Ser566Thr)	GPR153 (S566T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457516	NM_207370.4(GPR153):c.1687C>G (p.Pro563Ala)	GPR153 (P563A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355882	NM_207370.4(GPR153):c.1684C>T (p.Arg562Cys)	GPR153 (R562C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101509	NM_207370.4(GPR153):c.1676G>C (p.Gly559Ala)	GPR153 (G559A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542383	NM_207370.4(GPR153):c.1675G>A (p.Gly559Ser)	GPR153 (G559S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531370	NM_207370.4(GPR153):c.1667C>T (p.Ser556Leu)	GPR153 (S556L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490674	NM_207370.4(GPR153):c.1610C>G (p.Ala537Gly)	GPR153 (A537G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215619	NM_207370.4(GPR153):c.1607A>C (p.Glu536Ala)	GPR153 (E536A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263313	NM_207370.4(GPR153):c.1589A>C (p.Asp530Ala)	GPR153 (D530A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210395	NM_207370.4(GPR153):c.1580C>T (p.Ala527Val)	GPR153 (A527V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265913	NM_207370.4(GPR153):c.1567C>T (p.Pro523Ser)	GPR153 (P523S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491198	NM_207370.4(GPR153):c.1544T>A (p.Leu515Gln)	GPR153 (L515Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382234	NM_207370.4(GPR153):c.1505C>A (p.Ala502Asp)	GPR153 (A502D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101508	NM_207370.4(GPR153):c.1480G>A (p.Ala494Thr)	GPR153 (A494T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342817	NM_207370.4(GPR153):c.1474C>T (p.Arg492Cys)	GPR153 (R492C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282264	NM_207370.4(GPR153):c.1462G>A (p.Gly488Arg)	GPR153 (G488R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344921	NM_207370.4(GPR153):c.1441G>C (p.Gly481Arg)	GPR153 (G481R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357328	NM_207370.4(GPR153):c.1439C>T (p.Pro480Leu)	GPR153 (P480L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535001	NM_207370.4(GPR153):c.1438C>T (p.Pro480Ser)	GPR153 (P480S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208504	NM_207370.4(GPR153):c.1435C>G (p.Pro479Ala)	GPR153 (P479A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384649	NM_207370.4(GPR153):c.1407T>G (p.Asp469Glu)	GPR153 (D469E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495585	NM_207370.4(GPR153):c.1336G>A (p.Asp446Asn)	GPR153 (D446N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356323	NM_207370.4(GPR153):c.1331C>T (p.Ala444Val)	GPR153 (A444V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403451	NM_207370.4(GPR153):c.1310G>A (p.Arg437His)	GPR153 (R437H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216905	NM_207370.4(GPR153):c.1204G>T (p.Val402Leu)	GPR153 (V402L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101506	NM_207370.4(GPR153):c.1191C>A (p.His397Gln)	GPR153 (H397Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101505	NM_207370.4(GPR153):c.1169C>A (p.Pro390Gln)	GPR153 (P390Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101504	NM_207370.4(GPR153):c.1075G>A (p.Ala359Thr)	GPR153 (A359T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101503	NM_207370.4(GPR153):c.1058T>C (p.Val353Ala)	GPR153 (V353A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783275	NM_207370.4(GPR153):c.1040G>A (p.Gly347Asp)	GPR153 (G347D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2638121	NM_207370.4(GPR153):c.963C>T (p.Asp321=)	GPR153	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2356877	NM_207370.4(GPR153):c.952A>G (p.Met318Val)	GPR153 (M318V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380924	NM_207370.4(GPR153):c.931C>T (p.Arg311Trp)	GPR153 (R311W)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3282259	NM_207370.4(GPR153):c.911G>A (p.Arg304Gln)	GPR153 (R304Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245119	NM_207370.4(GPR153):c.910C>T (p.Arg304Trp)	GPR153 (R304W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101522	NM_207370.4(GPR153):c.904C>G (p.Arg302Gly)	GPR153 (R302G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411142	NM_207370.4(GPR153):c.896C>T (p.Ala299Val)	GPR153 (A299V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296416	NM_207370.4(GPR153):c.894G>C (p.Trp298Cys)	GPR153 (W298C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259246	NM_207370.4(GPR153):c.851G>T (p.Trp284Leu)	GPR153 (W284L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101521	NM_207370.4(GPR153):c.836C>T (p.Ala279Val)	GPR153 (A279V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 734251	NM_207370.4(GPR153):c.825G>A (p.Ala275=)	GPR153	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2570178	NM_207370.4(GPR153):c.824C>T (p.Ala275Val)	GPR153 (A275V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282262	NM_207370.4(GPR153):c.820T>G (p.Ser274Ala)	GPR153 (S274A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216867	NM_207370.4(GPR153):c.691G>A (p.Asp231Asn)	GPR153 (D231N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310045	NM_207370.4(GPR153):c.688A>G (p.Ile230Val)	GPR153 (I230V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101520	NM_207370.4(GPR153):c.676C>T (p.Arg226Trp)	GPR153 (R226W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208297	NM_207370.4(GPR153):c.665C>T (p.Ala222Val)	GPR153 (A222V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528102	NM_207370.4(GPR153):c.640G>A (p.Val214Met)	GPR153 (V214M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353159	NM_207370.4(GPR153):c.617A>G (p.Gln206Arg)	GPR153 (Q206R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3101519	NM_207370.4(GPR153):c.607G>A (p.Val203Met)	GPR153 (V203M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372035	NM_207370.4(GPR153):c.593C>T (p.Thr198Met)	GPR153 (T198M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460973	NM_207370.4(GPR153):c.577A>G (p.Ile193Val)	GPR153 (I193V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101518	NM_207370.4(GPR153):c.565A>G (p.Ile189Val)	GPR153 (I189V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3101516	NM_207370.4(GPR153):c.484C>T (p.Arg162Cys)	GPR153 (R162C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246200	NM_207370.4(GPR153):c.479G>A (p.Gly160Asp)	GPR153 (G160D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101515	NM_207370.4(GPR153):c.391G>A (p.Val131Ile)	GPR153 (V131I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101514	NM_207370.4(GPR153):c.380C>T (p.Ala127Val)	GPR153 (A127V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227817	NM_207370.4(GPR153):c.378G>C (p.Gln126His)	GPR153 (Q126H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282261	NM_207370.4(GPR153):c.363C>G (p.Ser121Arg)	GPR153 (S121R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101513	NM_207370.4(GPR153):c.331A>T (p.Met111Leu)	GPR153 (M111L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364783	NM_207370.4(GPR153):c.287C>T (p.Ala96Val)	GPR153 (A96V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783920	NM_207370.4(GPR153):c.283C>T (p.Leu95=)	GPR153	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2620359	NM_207370.4(GPR153):c.229G>A (p.Glu77Lys)	GPR153 (E77K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783276	NM_207370.4(GPR153):c.218G>A (p.Arg73His)	GPR153 (R73H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 208391	NM_207370.4(GPR153):c.217C>T (p.Arg73Cys)	GPR153 (R73C)	Single nucleotide variant (missense variant)	Childhood-onset schizophrenia	GLikely pathogenic
Select item 2512470	NM_207370.4(GPR153):c.212G>A (p.Arg71Gln)	GPR153 (R71Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507849	NM_207370.4(GPR153):c.209G>A (p.Arg70Gln)	GPR153 (R70Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362034	NM_207370.4(GPR153):c.181A>G (p.Ile61Val)	GPR153 (I61V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282260	NM_207370.4(GPR153):c.151G>A (p.Ala51Thr)	GPR153 (A51T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379835	NM_207370.4(GPR153):c.107A>T (p.Gln36Leu)	GPR153 (Q36L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209420	NM_207370.4(GPR153):c.100G>A (p.Ala34Thr)	GPR153 (A34T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604912	NM_207370.4(GPR153):c.62C>T (p.Ser21Phe)	GPR153 (S21F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282263	NM_207370.4(GPR153):c.51T>G (p.Cys17Trp)	GPR153 (C17W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101512	NM_207370.4(GPR153):c.32C>T (p.Ala11Val)	GPR153 (A11V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 80