ClinVar for Gene (Select 8787) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314141	NM_003835.4(RGS9):c.437T>C (p.Phe146Ser)	RGS9 (F146S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3314140	NM_003835.4(RGS9):c.1873A>G (p.Lys625Glu)	RGS9 (K625E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3314139	NM_003835.4(RGS9):c.458A>C (p.Tyr153Ser)	RGS9 (Y153S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3153934	NM_003835.4(RGS9):c.998A>G (p.Glu333Gly)	RGS9 (E330G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3153933	NM_003835.4(RGS9):c.541G>A (p.Asp181Asn)	RGS9 (D181N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3153932	NM_003835.4(RGS9):c.1763G>A (p.Arg588Gln)	RGS9 (R585Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3001860	NM_003835.4(RGS9):c.912C>T (p.Ser304=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2990598	NM_003835.4(RGS9):c.746+1G>C	RGS9	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2988697	NM_003835.4(RGS9):c.1758G>A (p.Leu586=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2980296	NM_003835.4(RGS9):c.205+12T>C	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2978772	NM_003835.4(RGS9):c.892C>A (p.Arg298=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2974190	NM_003835.4(RGS9):c.582+19G>C	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2970567	NM_003835.4(RGS9):c.333C>G (p.Thr111=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2962626	NM_003835.4(RGS9):c.1533C>T (p.Ser511=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2955669	NM_003835.4(RGS9):c.1375C>T (p.Arg459Ter)	RGS9 (R456* +1 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2914885	NM_003835.4(RGS9):c.825C>T (p.Thr275=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2896893	NM_003835.4(RGS9):c.1671C>T (p.Ser557=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2880692	NM_003835.4(RGS9):c.330C>T (p.Pro110=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2879685	NM_003835.4(RGS9):c.132C>T (p.Thr44=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2877229	NM_003835.4(RGS9):c.424-11T>C	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2875691	NM_003835.4(RGS9):c.1289+13A>G	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867673	NM_003835.4(RGS9):c.313-17C>G	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2845166	NM_003835.4(RGS9):c.1989A>G (p.Thr663=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2838251	NM_003835.4(RGS9):c.1892+19C>G	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2819055	NM_003835.4(RGS9):c.1605C>G (p.Gly535=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2812628	NM_003835.4(RGS9):c.1289+10A>G	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2811118	NM_003835.4(RGS9):c.39G>A (p.Arg13=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2810816	NM_003835.4(RGS9):c.976+10T>G	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2809367	NM_003835.4(RGS9):c.1746C>T (p.Phe582=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2789740	NM_003835.4(RGS9):c.58-6T>C	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2789306	NM_003835.4(RGS9):c.1416G>A (p.Gln472=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2787412	NM_003835.4(RGS9):c.99G>A (p.Gly33=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2785357	NM_003835.4(RGS9):c.1204-14C>G	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2779487	NM_003835.4(RGS9):c.681del (p.Glu228fs)	RGS9 (E225fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2779311	NM_003835.4(RGS9):c.177C>T (p.Ile59=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2758357	NM_003835.4(RGS9):c.501-17G>C	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2747926	NM_003835.4(RGS9):c.313-6T>C	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2710774	NM_003835.4(RGS9):c.474C>T (p.Val158=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2617080	NM_003835.4(RGS9):c.426A>T (p.Glu142Asp)	RGS9 (E142D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2552840	NM_003835.4(RGS9):c.1676C>T (p.Ala559Val)	RGS9 (A559V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2536173	NM_003835.4(RGS9):c.289G>C (p.Asp97His)	RGS9 (D97H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2518615	NM_003835.4(RGS9):c.332C>T (p.Thr111Ile)	RGS9 (T111I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2495741	NM_003835.4(RGS9):c.694T>A (p.Tyr232Asn)	RGS9 (Y232N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2474949	NM_003835.4(RGS9):c.631C>T (p.Pro211Ser)	RGS9 (P211S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2424775	NC_000017.10:g.(?_63149520)_(63149656_?)dup	RGS9	Duplication	not provided	GLikely pathogenic
Select item 2421575	NM_003835.4(RGS9):c.1312C>T (p.Arg438Cys)	RGS9 (R435C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2419472	NM_003835.4(RGS9):c.510G>A (p.Lys170=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2417935	NM_003835.4(RGS9):c.501-3C>A	RGS9	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2417377	NM_003835.4(RGS9):c.1372G>A (p.Ala458Thr)	RGS9 (A455T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2324687	NM_003835.4(RGS9):c.1301C>A (p.Pro434His)	RGS9 (P434H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2315138	NM_003835.4(RGS9):c.610G>A (p.Gly204Ser)	RGS9 (G204S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2267260	NM_003835.4(RGS9):c.521A>G (p.Lys174Arg)	RGS9 (K174R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2247622	NM_003835.4(RGS9):c.1643C>T (p.Pro548Leu)	RGS9 (P545L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2236004	NM_003835.4(RGS9):c.1876T>C (p.Ser626Pro)	RGS9 (S623P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2218188	NM_003835.4(RGS9):c.1700G>C (p.Arg567Pro)	RGS9 (R567P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2182194	NM_003835.4(RGS9):c.274C>G (p.Leu92Val)	RGS9 (L92V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2174658	NM_003835.4(RGS9):c.1888G>A (p.Ala630Thr)	RGS9 (A630T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2135718	NM_003835.4(RGS9):c.1064+19G>C	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2133057	NM_003835.4(RGS9):c.1892+17G>A	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2131824	NM_003835.4(RGS9):c.1065-5C>A	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2131692	NM_003835.4(RGS9):c.595A>G (p.Asn199Asp)	RGS9 (N199D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2129247	NM_003835.4(RGS9):c.1408-6C>G	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2129157	NM_003835.4(RGS9):c.365-7T>C	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2125990	NM_003835.4(RGS9):c.592G>A (p.Asp198Asn)	RGS9 (D198N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2125632	NM_003835.4(RGS9):c.713G>C (p.Arg238Thr)	RGS9 (R238T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2125009	NM_003835.4(RGS9):c.185G>T (p.Arg62Leu)	RGS9 (R62L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2123030	NM_003835.4(RGS9):c.1065-18A>G	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2119168	NM_003835.4(RGS9):c.1408-20T>G	RGS9	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2116071	NM_003835.4(RGS9):c.684+3A>C	RGS9	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2114892	NM_003835.4(RGS9):c.1684G>C (p.Asp562His)	RGS9 (D559H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2114877	NM_003835.4(RGS9):c.1935C>G (p.Thr645=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2110202	NM_003835.4(RGS9):c.545G>T (p.Cys182Phe)	RGS9 (C182F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2108473	NM_003835.4(RGS9):c.1767C>T (p.Gly589=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2107867	NM_003835.4(RGS9):c.781G>T (p.Asp261Tyr)	RGS9 (D258Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2105894	NM_003835.4(RGS9):c.1491C>T (p.Ser497=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2105888	NM_003835.4(RGS9):c.651C>A (p.Asn217Lys)	RGS9 (N217K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2104920	NM_003835.4(RGS9):c.205+2del	RGS9	Deletion (splice donor variant)	not provided	GLikely pathogenic
Select item 2104348	NM_003835.4(RGS9):c.583-19T>C	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2103281	NM_003835.4(RGS9):c.726G>A (p.Lys242=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2100181	NM_003835.4(RGS9):c.860+7A>G	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2099972	NM_003835.4(RGS9):c.1969G>C (p.Glu657Gln)	RGS9 (E654Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2097540	NM_003835.4(RGS9):c.206-1G>A	RGS9	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 2097499	NM_003835.4(RGS9):c.1933A>G (p.Thr645Ala)	RGS9 (T642A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2097326	NM_003835.4(RGS9):c.500+17C>T	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2096601	NM_003835.4(RGS9):c.237G>C (p.Arg79Ser)	RGS9 (R79S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2096420	NM_003835.4(RGS9):c.1499G>A (p.Cys500Tyr)	RGS9 (C500Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2094672	NM_003835.4(RGS9):c.1462A>G (p.Met488Val)	RGS9 (M485V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2091518	NM_003835.4(RGS9):c.364+20C>G	RGS9	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2088388	NM_003835.4(RGS9):c.1168G>A (p.Ala390Thr)	RGS9 (A387T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2085000	NM_003835.4(RGS9):c.1233G>A (p.Pro411=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2082262	NM_003835.4(RGS9):c.1679C>T (p.Ser560Phe)	RGS9 (S560F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2073786	NM_003835.4(RGS9):c.382C>T (p.Arg128Ter)	RGS9 (R128*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2072145	NM_003835.4(RGS9):c.1689C>T (p.Thr563=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2071020	NM_003835.4(RGS9):c.746+11G>A	RGS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2070865	NM_003835.4(RGS9):c.11G>T (p.Arg4Leu)	LOC130061461, RGS9 (R4L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2061246	NM_003835.4(RGS9):c.1376G>A (p.Arg459Gln)	RGS9 (R456Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2057427	NM_003835.4(RGS9):c.1397A>G (p.Asp466Gly)	RGS9 (D463G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2054874	NM_003835.4(RGS9):c.1565G>T (p.Cys522Phe)	RGS9 (C519F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2049226	NM_003835.4(RGS9):c.1467C>G (p.Pro489=)	RGS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2048019	NM_003835.4(RGS9):c.492G>T (p.Glu164Asp)	RGS9 (E164D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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