"Ambry Genetics"[submitter] AND "ARHGAP29"[gene] - ClinVar

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Items: 64

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2605117	NM_004815.4(ARHGAP29):c.3761A>G (p.Glu1254Gly)	ARHGAP29 (E1245G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3311531	NM_004815.4(ARHGAP29):c.3744A>T (p.Gln1248His)	ARHGAP29 (Q1184H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2591349	NM_004815.4(ARHGAP29):c.3712A>G (p.Met1238Val)	ARHGAP29 (M1229V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2313293	NM_004815.4(ARHGAP29):c.3701A>G (p.Asp1234Gly)	ARHGAP29 (D1170G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2291047	NM_004815.4(ARHGAP29):c.3688C>T (p.Leu1230Phe)	ARHGAP29 (L1221F +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2537163	NM_004815.4(ARHGAP29):c.3635C>A (p.Ala1212Glu)	ARHGAP29 (A1203E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128721	NM_004815.4(ARHGAP29):c.3587A>T (p.His1196Leu)	ARHGAP29 (H1187L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3311511	NM_004815.4(ARHGAP29):c.3586C>G (p.His1196Asp)	ARHGAP29 (H1196D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2382576	NM_004815.4(ARHGAP29):c.3235A>G (p.Lys1079Glu)	ARHGAP29 (K1079E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128720	NM_004815.4(ARHGAP29):c.3224A>C (p.Gln1075Pro)	ARHGAP29 (Q1011P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2402385	NM_004815.4(ARHGAP29):c.3218A>G (p.Asp1073Gly)	ARHGAP29 (D1064G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2300542	NM_004815.4(ARHGAP29):c.3212G>T (p.Gly1071Val)	ARHGAP29 (G1071V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2314896	NM_004815.4(ARHGAP29):c.3197G>T (p.Cys1066Phe)	ARHGAP29 (C1057F +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2227033	NM_004815.4(ARHGAP29):c.3010A>G (p.Asn1004Asp)	ARHGAP29 (N1004D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2510472	NM_004815.4(ARHGAP29):c.3007A>G (p.Thr1003Ala)	ARHGAP29 (T1003A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128719	NM_004815.4(ARHGAP29):c.2971A>G (p.Thr991Ala)	ARHGAP29 (T927A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2396246	NM_004815.4(ARHGAP29):c.2876C>T (p.Ala959Val)	ARHGAP29 (A895V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2463597	NM_004815.4(ARHGAP29):c.2804A>G (p.His935Arg)	ARHGAP29 (H926R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3311560	NM_004815.4(ARHGAP29):c.2773T>G (p.Ser925Ala)	ARHGAP29 (S861A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2257638	NM_004815.4(ARHGAP29):c.2726A>C (p.Lys909Thr)	ARHGAP29 (K845T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548172	NM_004815.4(ARHGAP29):c.2705T>C (p.Val902Ala)	ARHGAP29 (V838A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128718	NM_004815.4(ARHGAP29):c.2620T>A (p.Leu874Met)	ARHGAP29 (L865M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2306188	NM_004815.4(ARHGAP29):c.2576C>T (p.Pro859Leu)	ARHGAP29 (P795L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128717	NM_004815.4(ARHGAP29):c.2549T>C (p.Leu850Pro)	ARHGAP29 (L850P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128716	NM_004815.4(ARHGAP29):c.2434G>A (p.Ala812Thr)	ARHGAP29 (A748T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2485283	NM_004815.4(ARHGAP29):c.2398C>A (p.Leu800Ile)	ARHGAP29 (L791I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2267641	NM_004815.4(ARHGAP29):c.2395A>C (p.Ile799Leu)	ARHGAP29 (I735L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3311552	NM_004815.4(ARHGAP29):c.2375T>C (p.Met792Thr)	ARHGAP29 (M728T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3311493	NM_004815.4(ARHGAP29):c.2318T>G (p.Val773Gly)	ARHGAP29 (V773G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128715	NM_004815.4(ARHGAP29):c.2315A>T (p.His772Leu)	ARHGAP29 (H763L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2375318	NM_004815.4(ARHGAP29):c.2273G>T (p.Arg758Leu)	ARHGAP29 (R758L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2300541	NM_004815.4(ARHGAP29):c.2206T>C (p.Ser736Pro)	ARHGAP29 (S672P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128714	NM_004815.4(ARHGAP29):c.2050A>G (p.Ile684Val)	ARHGAP29 (I684V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2242467	NM_004815.4(ARHGAP29):c.1799C>T (p.Thr600Ile)	ARHGAP29 (T536I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128713	NM_004815.4(ARHGAP29):c.1694G>A (p.Arg565Gln)	ARHGAP29 (R501Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2489686	NM_004815.4(ARHGAP29):c.1691A>T (p.His564Leu)	ARHGAP29 (H564L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3311541	NM_004815.4(ARHGAP29):c.1614T>A (p.Phe538Leu)	ARHGAP29 (F474L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3311504	NM_004815.4(ARHGAP29):c.1493A>C (p.Asn498Thr)	ARHGAP29 (N434T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128712	NM_004815.4(ARHGAP29):c.1462A>G (p.Ser488Gly)	ARHGAP29 (S424G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2615012	NM_004815.4(ARHGAP29):c.1409C>G (p.Thr470Arg)	ARHGAP29 (T406R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2221725	NM_004815.4(ARHGAP29):c.1381C>G (p.Gln461Glu)	ARHGAP29 (Q397E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2307462	NM_004815.4(ARHGAP29):c.1288G>A (p.Val430Ile)	ARHGAP29 (V366I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3128711	NM_004815.4(ARHGAP29):c.1270A>G (p.Thr424Ala)	ARHGAP29 (T360A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2517046	NM_004815.4(ARHGAP29):c.1240C>T (p.Leu414Phe)	ARHGAP29 (L414F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2250572	NM_004815.4(ARHGAP29):c.1151A>C (p.Glu384Ala)	ARHGAP29 (E320A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2465557	NM_004815.4(ARHGAP29):c.1088A>G (p.Asn363Ser)	ARHGAP29 (N363S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2476933	NM_004815.4(ARHGAP29):c.1054G>C (p.Glu352Gln)	ARHGAP29 (E288Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2301883	NM_004815.4(ARHGAP29):c.928C>T (p.Leu310Phe)	ARHGAP29 (L246F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2515264	NM_004815.4(ARHGAP29):c.912G>T (p.Arg304Ser)	ARHGAP29 (R240S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2243631	NM_004815.4(ARHGAP29):c.898A>G (p.Met300Val)	ARHGAP29 (M300V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2318801	NM_004815.4(ARHGAP29):c.830T>C (p.Leu277Ser)	ARHGAP29 (L213S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2495163	NM_004815.4(ARHGAP29):c.821G>A (p.Ser274Asn)	ARHGAP29 (S210N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2526964	NM_004815.4(ARHGAP29):c.805A>G (p.Asn269Asp)	ARHGAP29 (N269D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128723	NM_004815.4(ARHGAP29):c.769A>G (p.Met257Val)	ARHGAP29 (M193V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3311570	NM_004815.4(ARHGAP29):c.712A>G (p.Arg238Gly)	ARHGAP29 (R238G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2265838	NM_004815.4(ARHGAP29):c.645G>T (p.Trp215Cys)	ARHGAP29 (W151C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2260067	NM_004815.4(ARHGAP29):c.640A>G (p.Thr214Ala)	ARHGAP29 (T214A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2348027	NM_004815.4(ARHGAP29):c.589G>A (p.Val197Met)	ARHGAP29 (V133M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2471080	NM_004815.4(ARHGAP29):c.485G>A (p.Arg162Gln)	ARHGAP29 (R162Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2368216	NM_004815.4(ARHGAP29):c.451C>T (p.Leu151Phe)	ARHGAP29 (L151F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3128722	NM_004815.4(ARHGAP29):c.419C>T (p.Ala140Val)	ARHGAP29 (A140V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3311521	NM_004815.4(ARHGAP29):c.413C>A (p.Thr138Asn)	ARHGAP29 (T138N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2558650	NM_004815.4(ARHGAP29):c.329C>A (p.Ala110Glu)	ARHGAP29 (A46E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355565	NM_004815.4(ARHGAP29):c.57A>C (p.Gln19His)	ARHGAP29 (Q19H)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance

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Items: 64