RGS3[gene] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 1 to 100 of 127

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 160862	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC124210612, LOC124210613 +3786 more	Copy number gain	See cases	GPathogenic
Select item 150340	GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	LOC121331326, LOC121331327 +3785 more	Copy number gain	See cases	GPathogenic
Select item 150050	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	LOC126860737, LOC126860738 +3786 more	Copy number gain	See cases	GPathogenic
Select item 149828	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 59875	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	LOC110121197, LOC110121234 +3786 more	Copy number gain	See cases	GPathogenic
Select item 33205	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC121331342, LOC121331343 +3786 more	Copy number gain	See cases	GPathogenic
Select item 153518	GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	LOC113839542, LOC113839543 +3786 more	Copy number gain	See cases	GPathogenic
Select item 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 144309	GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	LOC130002189, LOC130002190 +3786 more	Copy number gain	See cases	GPathogenic
Select item 59881	GRCh38/hg38 9q22.1-32(chr9:88522292-113687796)x3	LOC130002218, LOC130002219 +994 more	Copy number gain	See cases	GPathogenic
Select item 161058	GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1	LOC126860732, LOC126860733 +514 more	Copy number loss	See cases	GPathogenic
Select item 32222	GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1	ABCA1, ABITRAM +514 more	Copy number loss	See cases	GPathogenic
Select item 59123	GRCh38/hg38 9q22.33-33.1(chr9:99349916-115767475)x1	CT70, CTNNAL1 +509 more	Copy number loss	See cases	GPathogenic
Select item 152171	GRCh38/hg38 9q31.2-33.1(chr9:107530314-117965944)x1	PALM2AKAP2, PAPPA +377 more	Copy number loss	See cases	GPathogenic
Select item 2208730	NM_144488.8(RGS3):c.-203A>G	RGS3	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 3314112	NM_144488.8(RGS3):c.-164G>T	RGS3	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2290372	NM_144488.8(RGS3):c.-72C>T	RGS3	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2243515	NM_144488.8(RGS3):c.-65C>G	RGS3	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2369137	NM_144488.8(RGS3):c.-51C>T	RGS3	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3153902	NM_144488.8(RGS3):c.-9C>T	RGS3	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2275586	NM_001394167.1(RGS3):c.97A>G (p.Ile33Val)	RGS3 (I33V +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2390658	NM_001394167.1(RGS3):c.146G>T (p.Gly49Val)	RGS3 (G49V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282957	NM_001394167.1(RGS3):c.146G>A (p.Gly49Asp)	RGS3 (G51D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332829	NM_001394167.1(RGS3):c.179C>T (p.Pro60Leu)	RGS3 (P62L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314118	NM_001394167.1(RGS3):c.188A>C (p.Lys63Thr)	RGS3 (K63T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410140	NM_001394167.1(RGS3):c.241G>A (p.Val81Ile)	RGS3 (V81I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2619751	NM_001394167.1(RGS3):c.397C>T (p.Leu133Phe)	RGS3 (L133F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153906	NM_001394167.1(RGS3):c.457C>T (p.Arg153Trp)	RGS3 (R153W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294596	NM_001394167.1(RGS3):c.484C>T (p.Arg162Trp)	RGS3 (R162W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314114	NM_001394167.1(RGS3):c.493C>T (p.Arg165Trp)	RGS3 (R173W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153907	NM_001394167.1(RGS3):c.497C>T (p.Pro166Leu)	RGS3 (P168L +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3153908	NM_001394167.1(RGS3):c.529G>A (p.Gly177Ser)	RGS3 (G179S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153909	NM_001394167.1(RGS3):c.596T>C (p.Phe199Ser)	RGS3 (F199S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330467	NM_001394167.1(RGS3):c.610G>A (p.Asp204Asn)	RGS3 (D206N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483472	NM_001394167.1(RGS3):c.649C>A (p.Pro217Thr)	RGS3 (P219T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409814	NM_001394167.1(RGS3):c.769A>T (p.Ile257Phe)	RGS3 (I257F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153888	NM_001394167.1(RGS3):c.787A>G (p.Met263Val)	RGS3 (M265V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396406	NM_001394167.1(RGS3):c.797A>C (p.Gln266Pro)	RGS3 (Q274P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289218	NM_001394167.1(RGS3):c.881G>A (p.Arg294Gln)	RGS3 (R302Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153889	NM_001394167.1(RGS3):c.887A>G (p.Lys296Arg)	RGS3 (K127R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553261	NM_001394167.1(RGS3):c.899A>T (p.His300Leu)	RGS3 (H131L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324231	NM_001394167.1(RGS3):c.922C>G (p.Gln308Glu)	RGS3 (Q139E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366839	NM_001394167.1(RGS3):c.953G>A (p.Ser318Asn)	RGS3 (S320N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314115	NM_001394167.1(RGS3):c.1010G>A (p.Gly337Glu)	RGS3 (G337E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325039	NM_001394167.1(RGS3):c.1013G>A (p.Gly338Asp)	RGS3 (G346D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243597	NM_001394167.1(RGS3):c.1030G>A (p.Ala344Thr)	RGS3 (A344T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272167	NM_001394167.1(RGS3):c.1036T>C (p.Ser346Pro)	RGS3 (S346P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153890	NM_001394167.1(RGS3):c.1054A>C (p.Thr352Pro)	RGS3 (T360P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2659432	NM_001394167.1(RGS3):c.1084C>T (p.Leu362=)	RGS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3314123	NM_001394167.1(RGS3):c.1157G>A (p.Ser386Asn)	RGS3 (S217N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397021	NM_001394167.1(RGS3):c.1178G>T (p.Gly393Val)	RGS3 (G395V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2659433	NM_001394167.1(RGS3):c.1338+8C>T	RGS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2362862	NM_001394167.1(RGS3):c.1357C>A (p.Pro453Thr)	RGS3 (P455T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512831	NM_001394167.1(RGS3):c.1480C>T (p.Arg494Cys)	RGS3 (R325C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515060	NM_001394167.1(RGS3):c.1489G>A (p.Val497Ile)	RGS3 (V505I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325227	NM_001394167.1(RGS3):c.1583C>T (p.Ala528Val)	RGS3 (A530V +3 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2456923	NM_001394167.1(RGS3):c.1649C>T (p.Ser550Leu)	RGS3 (S552L +3 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2603558	NM_001394167.1(RGS3):c.1792C>G (p.Pro598Ala)	RGS3 (P600A +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494946	NM_001394167.1(RGS3):c.1862A>G (p.Glu621Gly)	RGS3 (E54G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542461	NM_001394167.1(RGS3):c.1897G>A (p.Asp633Asn)	RGS3 (D633N +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314120	NM_001394167.1(RGS3):c.1898A>G (p.Asp633Gly)	RGS3 (D641G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 770753	NM_001394167.1(RGS3):c.1940C>T (p.Pro647Leu)	RGS3 (P478L +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2323590	NM_001394167.1(RGS3):c.1961C>T (p.Pro654Leu)	RGS3 (P105L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206529	NM_001394167.1(RGS3):c.1986A>T (p.Gln662His)	RGS3 (Q113H +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288591	NM_001394167.1(RGS3):c.2092G>T (p.Asp698Tyr)	RGS3 (D706Y +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153892	NM_001394167.1(RGS3):c.2132C>T (p.Ser711Phe)	RGS3 (S713F +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153893	NM_001394167.1(RGS3):c.2144A>G (p.Lys715Arg)	RGS3 (K166R +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454439	NM_001394167.1(RGS3):c.2167A>G (p.Ser723Gly)	RGS3 (S554G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314122	NM_001394167.1(RGS3):c.2168G>A (p.Ser723Asn)	RGS3 (S554N +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395952	NM_001394167.1(RGS3):c.2173G>A (p.Gly725Arg)	RGS3 (G158R +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473844	NM_001394167.1(RGS3):c.2192C>G (p.Thr731Ser)	RGS3 (T731S +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2659434	NM_001394167.1(RGS3):c.2203C>T (p.Pro735Ser)	RGS3 (P168S +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2494783	NM_001394167.1(RGS3):c.2227G>A (p.Val743Met)	RGS3 (V194M +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394755	NM_001394167.1(RGS3):c.2249A>C (p.Asp750Ala)	RGS3 (D183A +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153895	NM_001394167.1(RGS3):c.2320G>A (p.Glu774Lys)	RGS3 (E207K +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314119	NM_001394167.1(RGS3):c.2327T>G (p.Val776Gly)	RGS3 (V209G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2544801	NM_001394167.1(RGS3):c.2335G>T (p.Gly779Trp)	RGS3 (G212W +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379697	NM_001394167.1(RGS3):c.2366A>C (p.Asp789Ala)	RGS3 (D620A +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221522	NM_001394167.1(RGS3):c.2386G>A (p.Gly796Arg)	RGS3 (G229R +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363945	NM_001394167.1(RGS3):c.2432A>G (p.Gln811Arg)	RGS3 (Q262R +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334115	NM_001394167.1(RGS3):c.2464C>A (p.Gln822Lys)	RGS3 (Q273K +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153897	NM_001394167.1(RGS3):c.2471C>T (p.Ser824Leu)	RGS3 (S655L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153898	NM_001394167.1(RGS3):c.2473C>G (p.Leu825Val)	RGS3 (L276V +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153899	NM_001394167.1(RGS3):c.2476C>T (p.Arg826Trp)	RGS3 (R259W +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391111	NM_001394167.1(RGS3):c.2479C>T (p.Arg827Cys)	RGS3 (R827C +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 774431	NM_001394167.1(RGS3):c.2487G>A (p.Thr829=)	RGS3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2458361	NM_001394167.1(RGS3):c.2540A>G (p.Asp847Gly)	RGS3 (D855G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559715	NM_001394167.1(RGS3):c.2558C>T (p.Ser853Leu)	RGS3 (S286L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314116	NM_001394167.1(RGS3):c.2572G>A (p.Ala858Thr)	RGS3 (A858T +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2209451	NM_001394167.1(RGS3):c.2579C>T (p.Ser860Phe)	RGS3 (S293F +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615144	NM_001394167.1(RGS3):c.2605A>T (p.Thr869Ser)	RGS3 (T302S +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261275	NM_001394167.1(RGS3):c.2623G>A (p.Gly875Ser)	RGS3 (G326S +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314121	NM_001394167.1(RGS3):c.2656C>T (p.Leu886Phe)	RGS3 (L717F +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407337	NM_001394167.1(RGS3):c.2676G>T (p.Arg892Ser)	RGS3 (R723S +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153901	NM_001394167.1(RGS3):c.2682G>A (p.Met894Ile)	RGS3 (M399I +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614639	NM_001394167.1(RGS3):c.2741A>G (p.Asn914Ser)	RGS3 (N419S +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314111	NM_001394167.1(RGS3):c.2812G>A (p.Ala938Thr)	RGS3 (A20T +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513618	NM_001394167.1(RGS3):c.2828A>C (p.Lys943Thr)	RGS3 (K943T +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534139	NM_001394167.1(RGS3):c.2864C>T (p.Ala955Val)	RGS3 (A388V +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296660	NM_001394167.1(RGS3):c.2878G>A (p.Glu960Lys)	RGS3 (E393K +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 2