ClinVar for Gene (Select 57584) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3128608	NM_020824.4(ARHGAP21):c.778T>A (p.Ser260Thr)	ARHGAP21 (S103T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128607	NM_020824.4(ARHGAP21):c.777A>T (p.Lys259Asn)	ARHGAP21 (K161N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128606	NM_020824.4(ARHGAP21):c.733A>G (p.Arg245Gly)	ARHGAP21 (R245G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128605	NM_020824.4(ARHGAP21):c.5822C>G (p.Pro1941Arg)	ARHGAP21 (P1931R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128604	NM_020824.4(ARHGAP21):c.5821C>A (p.Pro1941Thr)	ARHGAP21 (P1728T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128603	NM_020824.4(ARHGAP21):c.5569C>T (p.Arg1857Cys)	ARHGAP21 (R1759C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128602	NM_020824.4(ARHGAP21):c.5503G>T (p.Val1835Leu)	ARHGAP21 (V1678L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128601	NM_020824.4(ARHGAP21):c.5479G>A (p.Glu1827Lys)	ARHGAP21 (E1614K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128600	NM_020824.4(ARHGAP21):c.5362G>C (p.Val1788Leu)	ARHGAP21 (V1778L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128599	NM_020824.4(ARHGAP21):c.5254G>A (p.Gly1752Ser)	ARHGAP21 (G1654S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3128598	NM_020824.4(ARHGAP21):c.5029A>C (p.Thr1677Pro)	ARHGAP21 (T1520P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128597	NM_020824.4(ARHGAP21):c.4997G>A (p.Arg1666Gln)	ARHGAP21 (R1453Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128596	NM_020824.4(ARHGAP21):c.4891C>T (p.Arg1631Trp)	ARHGAP21 (R1631W +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128595	NM_020824.4(ARHGAP21):c.4831G>A (p.Val1611Met)	ARHGAP21 (V1398M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128594	NM_020824.4(ARHGAP21):c.4821G>C (p.Glu1607Asp)	ARHGAP21 (E1509D +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128593	NM_020824.4(ARHGAP21):c.4793G>T (p.Ser1598Ile)	ARHGAP21 (S1500I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128591	NM_020824.4(ARHGAP21):c.4459A>G (p.Lys1487Glu)	ARHGAP21 (K1274E +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128590	NM_020824.4(ARHGAP21):c.4321T>A (p.Phe1441Ile)	ARHGAP21 (F1284I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128589	NM_020824.4(ARHGAP21):c.4315A>G (p.Asn1439Asp)	ARHGAP21 (N1226D +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128588	NM_020824.4(ARHGAP21):c.4223T>C (p.Leu1408Pro)	ARHGAP21 (L1398P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128587	NM_020824.4(ARHGAP21):c.347C>G (p.Ala116Gly)	ARHGAP21 (A116G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3128586	NM_020824.4(ARHGAP21):c.3352A>G (p.Lys1118Glu)	ARHGAP21 (K961E +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128585	NM_020824.4(ARHGAP21):c.3239G>A (p.Ser1080Asn)	ARHGAP21 (S1080N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128584	NM_020824.4(ARHGAP21):c.3013A>T (p.Arg1005Trp)	ARHGAP21 (R907W +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128583	NM_020824.4(ARHGAP21):c.2927A>C (p.Lys976Thr)	ARHGAP21 (K966T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128582	NM_020824.4(ARHGAP21):c.2867G>A (p.Arg956Gln)	ARHGAP21 (R743Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128581	NM_020824.4(ARHGAP21):c.2822G>A (p.Arg941Gln)	ARHGAP21 (R728Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128580	NM_020824.4(ARHGAP21):c.2698G>C (p.Val900Leu)	ARHGAP21 (V900L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128579	NM_020824.4(ARHGAP21):c.2615C>T (p.Pro872Leu)	ARHGAP21 (P659L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128578	NM_020824.4(ARHGAP21):c.2332C>T (p.Arg778Cys)	ARHGAP21 (R778C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128577	NM_020824.4(ARHGAP21):c.1825C>T (p.Arg609Trp)	ARHGAP21 (R396W +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128576	NM_020824.4(ARHGAP21):c.1718G>A (p.Ser573Asn)	ARHGAP21 (S416N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128575	NM_020824.4(ARHGAP21):c.1652A>G (p.Lys551Arg)	ARHGAP21 (K338R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128574	NM_020824.4(ARHGAP21):c.1556A>G (p.Asn519Ser)	ARHGAP21 (N306S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128573	NM_020824.4(ARHGAP21):c.1519G>A (p.Glu507Lys)	ARHGAP21 (E294K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128572	NM_020824.4(ARHGAP21):c.1460G>A (p.Ser487Asn)	ARHGAP21 (S389N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128571	NM_020824.4(ARHGAP21):c.1294C>T (p.Arg432Cys)	ARHGAP21 (R334C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128570	NM_020824.4(ARHGAP21):c.1055G>T (p.Ser352Ile)	ARHGAP21 (S195I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2684600	GRCh37/hg19 10p12.2-12.1(chr10:24560328-25536166)x3	ARHGAP21, ENKUR +4 more	Copy number gain	not provided	GUncertain significance
Select item 2640356	NM_020824.4(ARHGAP21):c.1689C>T (p.Ser563=)	ARHGAP21	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2640355	NM_020824.4(ARHGAP21):c.2310C>T (p.Thr770=)	ARHGAP21	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2640354	NM_020824.4(ARHGAP21):c.2343C>T (p.Val781=)	ARHGAP21	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2640353	NM_020824.4(ARHGAP21):c.3438C>T (p.Gly1146=)	ARHGAP21	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2640352	NM_020824.4(ARHGAP21):c.5107C>T (p.Leu1703Phe)	ARHGAP21 (L1490F +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2640351	NM_020824.4(ARHGAP21):c.5214A>G (p.Lys1738=)	ARHGAP21	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2640350	NM_020824.4(ARHGAP21):c.5835T>A (p.Ser1945=)	ARHGAP21	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2624167	NM_020824.4(ARHGAP21):c.1315C>T (p.Arg439Cys)	ARHGAP21 (R429C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620758	NM_020824.4(ARHGAP21):c.5600G>A (p.Arg1867Lys)	ARHGAP21 (R1857K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615828	NM_020824.4(ARHGAP21):c.5567A>G (p.Glu1856Gly)	ARHGAP21 (E1643G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614446	NM_020824.4(ARHGAP21):c.329G>T (p.Gly110Val)	ARHGAP21 (G110V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2604047	NM_020824.4(ARHGAP21):c.2077G>T (p.Ala693Ser)	ARHGAP21 (A536S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601507	NM_020824.4(ARHGAP21):c.3255G>T (p.Leu1085Phe)	ARHGAP21 (L1075F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601365	NM_020824.4(ARHGAP21):c.4427A>G (p.Glu1476Gly)	ARHGAP21 (E1263G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595491	NM_020824.4(ARHGAP21):c.469C>A (p.Pro157Thr)	ARHGAP21 (P157T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2591931	NM_020824.4(ARHGAP21):c.4385G>A (p.Ser1462Asn)	ARHGAP21 (S1305N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2574696	GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	MTG1, NPS +679 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2574686	GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	A1CF, ABCC2 +670 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 2551288	NM_020824.4(ARHGAP21):c.1036C>T (p.Leu346Phe)	ARHGAP21 (L133F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2547721	NM_020824.4(ARHGAP21):c.856T>G (p.Ser286Ala)	ARHGAP21 (S276A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546738	NM_020824.4(ARHGAP21):c.4908C>A (p.Asp1636Glu)	ARHGAP21 (D1423E +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544629	NM_020824.4(ARHGAP21):c.731A>G (p.Tyr244Cys)	ARHGAP21 (Y234C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541743	NM_020824.4(ARHGAP21):c.1874C>A (p.Ser625Tyr)	ARHGAP21 (S468Y +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541002	NM_020824.4(ARHGAP21):c.2776T>A (p.Ser926Thr)	ARHGAP21 (S769T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540502	NM_020824.4(ARHGAP21):c.4096G>A (p.Asp1366Asn)	ARHGAP21 (D1268N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533274	NM_020824.4(ARHGAP21):c.4875A>T (p.Glu1625Asp)	ARHGAP21 (E1412D +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530498	NM_020824.4(ARHGAP21):c.2741C>T (p.Ser914Leu)	ARHGAP21 (S904L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527440	NM_020824.4(ARHGAP21):c.5780A>C (p.Gln1927Pro)	ARHGAP21 (Q1770P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520253	NM_020824.4(ARHGAP21):c.2087C>T (p.Ser696Leu)	ARHGAP21 (S483L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519071	NM_020824.4(ARHGAP21):c.238T>C (p.Tyr80His)	ARHGAP21 (Y80H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2518641	NM_020824.4(ARHGAP21):c.2698G>A (p.Val900Ile)	ARHGAP21 (V687I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512556	NM_020824.4(ARHGAP21):c.3101C>T (p.Thr1034Met)	ARHGAP21 (T1024M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508925	NM_020824.4(ARHGAP21):c.5434G>A (p.Glu1812Lys)	ARHGAP21 (E1599K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483369	NM_020824.4(ARHGAP21):c.4631C>G (p.Ser1544Cys)	ARHGAP21 (S1534C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481843	NM_020824.4(ARHGAP21):c.1613G>A (p.Arg538Gln)	ARHGAP21 (R325Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474031	NM_020824.4(ARHGAP21):c.346G>A (p.Ala116Thr)	ARHGAP21 (A18T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2467920	NM_020824.4(ARHGAP21):c.5744C>T (p.Pro1915Leu)	ARHGAP21 (P1915L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462561	NM_020824.4(ARHGAP21):c.5575C>T (p.Arg1859Cys)	ARHGAP21 (R1702C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460074	NM_020824.4(ARHGAP21):c.647A>G (p.Gln216Arg)	ARHGAP21 (Q206R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408291	NM_020824.4(ARHGAP21):c.2558G>A (p.Arg853His)	ARHGAP21 (R640H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405257	NM_020824.4(ARHGAP21):c.722G>C (p.Gly241Ala)	ARHGAP21 (G231A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399361	NM_020824.4(ARHGAP21):c.2593C>T (p.Pro865Ser)	ARHGAP21 (P652S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384291	NM_020824.4(ARHGAP21):c.881C>T (p.Pro294Leu)	ARHGAP21 (P196L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370190	NM_020824.4(ARHGAP21):c.38A>G (p.Asp13Gly)	ARHGAP21 (D13G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2365737	NM_020824.4(ARHGAP21):c.1892C>T (p.Thr631Met)	ARHGAP21 (T418M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2355121	NM_020824.4(ARHGAP21):c.1295G>A (p.Arg432His)	ARHGAP21 (R275H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340997	NM_020824.4(ARHGAP21):c.1529A>G (p.Asn510Ser)	ARHGAP21 (N500S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2333431	NM_020824.4(ARHGAP21):c.2146T>A (p.Leu716Ile)	ARHGAP21 (L559I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2332741	NM_020824.4(ARHGAP21):c.4436C>A (p.Thr1479Asn)	ARHGAP21 (T1469N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322124	NM_020824.4(ARHGAP21):c.3116G>A (p.Ser1039Asn)	ARHGAP21 (S1039N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314702	NM_020824.4(ARHGAP21):c.4655C>T (p.Thr1552Met)	ARHGAP21 (T1339M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314595	NM_020824.4(ARHGAP21):c.4835C>T (p.Ala1612Val)	ARHGAP21 (A1455V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2310998	NM_020824.4(ARHGAP21):c.155C>G (p.Thr52Arg)	ARHGAP21 (T52R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2306105	NM_020824.4(ARHGAP21):c.2845A>G (p.Lys949Glu)	ARHGAP21 (K736E +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293409	NM_020824.4(ARHGAP21):c.1028G>A (p.Gly343Glu)	ARHGAP21 (G333E +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2290142	NM_020824.4(ARHGAP21):c.641T>C (p.Met214Thr)	ARHGAP21 (M1T +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2290139	NM_020824.4(ARHGAP21):c.5758C>A (p.Gln1920Lys)	ARHGAP21 (Q1763K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270607	NM_020824.4(ARHGAP21):c.3481A>G (p.Ile1161Val)	ARHGAP21 (I1063V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2264375	NM_020824.4(ARHGAP21):c.2431A>G (p.Thr811Ala)	ARHGAP21 (T811A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2263551	NM_020824.4(ARHGAP21):c.5198T>C (p.Val1733Ala)	ARHGAP21 (V1733A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262602	NM_020824.4(ARHGAP21):c.1877T>C (p.Leu626Pro)	ARHGAP21 (L413P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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