"Ambry Genetics"[submitter] AND "RGS11"[gene] - ClinVar

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Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3153769	NM_183337.3(RGS11):c.1394G>A (p.Gly465Glu)	FAM234A, RGS11 (G281E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519954	NM_183337.3(RGS11):c.1349C>G (p.Thr450Ser)	FAM234A, RGS11 (T439S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153768	NM_183337.3(RGS11):c.1288C>T (p.Arg430Cys)	FAM234A, RGS11 (R430C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314073	NM_183337.3(RGS11):c.1277A>C (p.Glu426Ala)	FAM234A, RGS11 (E405A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153766	NM_183337.3(RGS11):c.1162G>A (p.Val388Ile)	RGS11 (V377I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519220	NM_183337.3(RGS11):c.1138G>A (p.Gly380Arg)	RGS11 (G359R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153764	NM_183337.3(RGS11):c.1084G>A (p.Gly362Arg)	RGS11 (G351R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153763	NM_183337.3(RGS11):c.1066G>A (p.Glu356Lys)	RGS11 (E172K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153762	NM_183337.3(RGS11):c.1042C>T (p.Pro348Ser)	RGS11 (P337S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545423	NM_183337.3(RGS11):c.1028C>T (p.Ala343Val)	RGS11 (A159V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314071	NM_183337.3(RGS11):c.1025G>T (p.Gly342Val)	RGS11 (G158V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481448	NM_183337.3(RGS11):c.1019G>A (p.Arg340Gln)	RGS11 (R319Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153785	NM_183337.3(RGS11):c.934G>A (p.Val312Met)	RGS11 (V301M +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2398083	NM_183337.3(RGS11):c.914G>C (p.Arg305Pro)	RGS11 (R305P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323449	NM_183337.3(RGS11):c.886C>T (p.Arg296Cys)	RGS11 (R275C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256414	NM_183337.3(RGS11):c.883C>T (p.Leu295Phe)	RGS11 (L295F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356282	NM_183337.3(RGS11):c.877A>T (p.Thr293Ser)	RGS11 (T272S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153784	NM_183337.3(RGS11):c.851T>C (p.Met284Thr)	RGS11 (M263T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379058	NM_183337.3(RGS11):c.838G>A (p.Ala280Thr)	RGS11 (A259T +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2608932	NM_183337.3(RGS11):c.797C>T (p.Ser266Leu)	RGS11 (S82L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399778	NM_183337.3(RGS11):c.793G>A (p.Val265Met)	RGS11 (V244M +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2287201	NM_183337.3(RGS11):c.773G>C (p.Arg258Pro)	RGS11 (R237P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404330	NM_183337.3(RGS11):c.691G>A (p.Glu231Lys)	RGS11 (E220K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367103	NM_183337.3(RGS11):c.602A>G (p.Asp201Gly)	RGS11 (D190G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455679	NM_183337.3(RGS11):c.601G>A (p.Asp201Asn)	RGS11 (D201N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3153783	NM_183337.3(RGS11):c.592G>A (p.Gly198Arg)	RGS11 (G198R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314075	NM_183337.3(RGS11):c.589C>G (p.Pro197Ala)	RGS11 (P186A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366675	NM_183337.3(RGS11):c.587C>T (p.Pro196Leu)	RGS11 (P185L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268974	NM_183337.3(RGS11):c.587C>A (p.Pro196Gln)	RGS11 (P175Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153781	NM_183337.3(RGS11):c.583C>G (p.Pro195Ala)	RGS11 (P174A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153780	NM_183337.3(RGS11):c.581G>C (p.Arg194Thr)	RGS11 (R183T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153779	NM_183337.3(RGS11):c.508G>A (p.Ala170Thr)	RGS11 (A149T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153778	NM_183337.3(RGS11):c.499C>A (p.Gln167Lys)	RGS11 (Q167K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352165	NM_183337.3(RGS11):c.467C>A (p.Ala156Glu)	RGS11 (A135E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153777	NM_183337.3(RGS11):c.443G>A (p.Arg148Gln)	RGS11 (R137Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3153776	NM_183337.3(RGS11):c.403C>T (p.Arg135Trp)	RGS11 (R114W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153775	NM_183337.3(RGS11):c.398G>A (p.Arg133Gln)	RGS11 (R112Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260416	NM_183337.3(RGS11):c.395T>G (p.Ile132Ser)	RGS11 (I121S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525722	NM_183337.3(RGS11):c.353C>T (p.Ala118Val)	RGS11 (A118V +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2466369	NM_183337.3(RGS11):c.323C>T (p.Pro108Leu)	RGS11 (P108L +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2370886	NM_183337.3(RGS11):c.320C>T (p.Thr107Ile)	RGS11 (T86I +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2210996	NM_183337.3(RGS11):c.305C>T (p.Pro102Leu)	RGS11 (P81L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153773	NM_183337.3(RGS11):c.260C>T (p.Pro87Leu)	RGS11 (P66L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153771	NM_183337.3(RGS11):c.168C>A (p.Asp56Glu)	RGS11 (D35E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153770	NM_183337.3(RGS11):c.148C>T (p.His50Tyr)	RGS11 (H29Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153765	NM_183337.3(RGS11):c.112A>G (p.Met38Val)	RGS11 (M38V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2240294	NM_183337.3(RGS11):c.80T>G (p.Val27Gly)	RGS11 (V6G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350942	NM_183337.3(RGS11):c.79G>A (p.Val27Met)	RGS11 (V6M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314070	NM_183337.3(RGS11):c.47T>A (p.Met16Lys)	RGS11 (M16K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314072	NM_183337.3(RGS11):c.32G>T (p.Arg11Leu)	RGS11 (R11L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153772	NM_183337.3(RGS11):c.22C>T (p.Pro8Ser)	RGS11 (P8S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 51