ANKRD31[gene] and "single gene"[properties] - ClinVar - NCBI

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

Search results

Items: 1 to 100 of 125

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2363506	NM_001372053.1(ANKRD31):c.5714G>A (p.Ser1905Asn)	ANKRD31 (S1848N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328615	NM_001372053.1(ANKRD31):c.5689C>A (p.Gln1897Lys)	ANKRD31 (Q1840K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125622	NM_001372053.1(ANKRD31):c.5660A>G (p.Glu1887Gly)	ANKRD31 (E1887G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228456	NM_001372053.1(ANKRD31):c.5613C>G (p.Asn1871Lys)	ANKRD31 (N1871K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125616	NM_001372053.1(ANKRD31):c.5607A>T (p.Glu1869Asp)	ANKRD31 (E1812D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363724	NM_001372053.1(ANKRD31):c.5482C>T (p.Leu1828Phe)	ANKRD31 (L1771F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125612	NM_001372053.1(ANKRD31):c.5441G>A (p.Ser1814Asn)	ANKRD31 (S1757N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400462	NM_001372053.1(ANKRD31):c.5231A>G (p.Asn1744Ser)	ANKRD31 (N1687S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476689	NM_001372053.1(ANKRD31):c.5200G>C (p.Gly1734Arg)	ANKRD31 (G1734R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253460	NM_001372053.1(ANKRD31):c.5179A>G (p.Ile1727Val)	ANKRD31 (I1670V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406171	NM_001372053.1(ANKRD31):c.5134C>T (p.Leu1712Phe)	ANKRD31 (L1655F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462361	NM_001372053.1(ANKRD31):c.5105G>A (p.Ser1702Asn)	ANKRD31 (S1645N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226886	NM_001372053.1(ANKRD31):c.5086G>A (p.Gly1696Arg)	ANKRD31 (G1639R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125588	NM_001372053.1(ANKRD31):c.5048A>G (p.Gln1683Arg)	ANKRD31 (Q1626R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791397	NM_001372053.1(ANKRD31):c.4918G>A (p.Gly1640Ser)	ANKRD31 (G1640S +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2260213	NM_001372053.1(ANKRD31):c.4876A>G (p.Thr1626Ala)	ANKRD31 (T1626A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125577	NM_001372053.1(ANKRD31):c.4864C>G (p.Leu1622Val)	ANKRD31 (L1622V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125572	NM_001372053.1(ANKRD31):c.4810T>G (p.Ser1604Ala)	ANKRD31 (S1547A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520870	NM_001372053.1(ANKRD31):c.4748G>A (p.Cys1583Tyr)	ANKRD31 (C1526Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297384	NM_001372053.1(ANKRD31):c.4738G>T (p.Gly1580Cys)	ANKRD31 (G1523C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241243	NM_001372053.1(ANKRD31):c.4718A>T (p.Asp1573Val)	ANKRD31 (D1516V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346961	NM_001372053.1(ANKRD31):c.4601C>T (p.Pro1534Leu)	ANKRD31 (P1477L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492920	NM_001372053.1(ANKRD31):c.4589G>A (p.Gly1530Asp)	ANKRD31 (G1473D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381115	NM_001372053.1(ANKRD31):c.4580C>T (p.Pro1527Leu)	ANKRD31 (P1470L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559418	NM_001372053.1(ANKRD31):c.4487C>T (p.Pro1496Leu)	ANKRD31 (P1439L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297402	NM_001372053.1(ANKRD31):c.4433A>G (p.Lys1478Arg)	ANKRD31 (K1421R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297375	NM_001372053.1(ANKRD31):c.4358T>G (p.Phe1453Cys)	ANKRD31 (F1453C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360647	NM_001372053.1(ANKRD31):c.4354T>C (p.Ser1452Pro)	ANKRD31 (S1395P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458175	NM_001372053.1(ANKRD31):c.4261A>G (p.Met1421Val)	ANKRD31 (M1364V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255549	NM_001372053.1(ANKRD31):c.4241C>A (p.Ala1414Glu)	ANKRD31 (A1414E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458324	NM_001372053.1(ANKRD31):c.4229A>G (p.Asn1410Ser)	ANKRD31 (N1410S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336901	NM_001372053.1(ANKRD31):c.4172C>T (p.Ala1391Val)	ANKRD31 (A1391V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344218	NM_001372053.1(ANKRD31):c.4135T>C (p.Ser1379Pro)	ANKRD31 (S1379P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539951	NM_001372053.1(ANKRD31):c.4109C>T (p.Ser1370Leu)	ANKRD31 (S1313L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378195	NM_001372053.1(ANKRD31):c.4079G>A (p.Cys1360Tyr)	ANKRD31 (C1360Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 770719	NM_001372053.1(ANKRD31):c.4058G>A (p.Arg1353Gln)	ANKRD31 (R1296Q +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2457937	NM_001372053.1(ANKRD31):c.4052C>T (p.Ala1351Val)	ANKRD31 (A1294V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125499	NM_001372053.1(ANKRD31):c.4044A>T (p.Lys1348Asn)	ANKRD31 (K1291N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294843	NM_001372053.1(ANKRD31):c.4006G>A (p.Val1336Ile)	ANKRD31 (V1336I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297395	NM_001372053.1(ANKRD31):c.3933G>T (p.Gln1311His)	ANKRD31 (Q1254H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365454	NM_001372053.1(ANKRD31):c.3922G>T (p.Asp1308Tyr)	ANKRD31 (D1251Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125487	NM_001372053.1(ANKRD31):c.3904G>A (p.Ala1302Thr)	ANKRD31 (A1245T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606997	NM_001372053.1(ANKRD31):c.3893T>G (p.Leu1298Arg)	ANKRD31 (L1298R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1924689	NM_001372053.1(ANKRD31):c.3880G>A (p.Ala1294Thr)	ANKRD31 (A1294T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2269718	NM_001372053.1(ANKRD31):c.3833G>A (p.Gly1278Glu)	ANKRD31 (G1221E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125469	NM_001372053.1(ANKRD31):c.3650A>G (p.His1217Arg)	ANKRD31 (H1160R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392290	NM_001372053.1(ANKRD31):c.3641G>C (p.Ser1214Thr)	ANKRD31 (S1214T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329762	NM_001372053.1(ANKRD31):c.3641G>A (p.Ser1214Asn)	ANKRD31 (S1214N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396496	NM_001372053.1(ANKRD31):c.3415C>T (p.His1139Tyr)	ANKRD31 (H1139Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596742	NM_001372053.1(ANKRD31):c.3377T>A (p.Ile1126Asn)	ANKRD31 (I1126N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125451	NM_001372053.1(ANKRD31):c.3369G>C (p.Leu1123Phe)	ANKRD31 (L1123F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376646	NM_001372053.1(ANKRD31):c.3359G>A (p.Ser1120Asn)	ANKRD31 (S1120N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2297465	NM_001372053.1(ANKRD31):c.3269T>C (p.Ile1090Thr)	ANKRD31 (I1090T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125441	NM_001372053.1(ANKRD31):c.3254C>T (p.Ala1085Val)	ANKRD31 (A1085V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3125434	NM_001372053.1(ANKRD31):c.3187A>G (p.Thr1063Ala)	ANKRD31 (T1063A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297354	NM_001372053.1(ANKRD31):c.3112A>G (p.Ile1038Val)	ANKRD31 (I1038V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526140	NM_001372053.1(ANKRD31):c.3061G>A (p.Ala1021Thr)	ANKRD31 (A1021T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125429	NM_001372053.1(ANKRD31):c.2987C>G (p.Pro996Arg)	ANKRD31 (P996R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125426	NM_001372053.1(ANKRD31):c.2960C>T (p.Ala987Val)	ANKRD31 (A987V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2630653	NM_001372053.1(ANKRD31):c.2933A>G (p.Asp978Gly)	ANKRD31 (D978G)	Single nucleotide variant (missense variant)	ANKRD31-related disorder	GUncertain significance
Select item 2515009	NM_001372053.1(ANKRD31):c.2906A>T (p.Gln969Leu)	ANKRD31 (Q969L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125419	NM_001372053.1(ANKRD31):c.2875A>C (p.Lys959Gln)	ANKRD31 (K959Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2381264	NM_001372053.1(ANKRD31):c.2737A>G (p.Ile913Val)	ANKRD31 (I913V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2612171	NM_001372053.1(ANKRD31):c.2702A>T (p.Asp901Val)	ANKRD31 (D901V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244569	NM_001372053.1(ANKRD31):c.2675C>A (p.Ser892Tyr)	ANKRD31 (S892Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125404	NM_001372053.1(ANKRD31):c.2618A>G (p.Asn873Ser)	ANKRD31 (N873S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 732785	NM_001372053.1(ANKRD31):c.2535A>T (p.Glu845Asp)	ANKRD31 (E845D)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2355908	NM_001372053.1(ANKRD31):c.2441A>G (p.Asp814Gly)	ANKRD31 (D814G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125397	NM_001372053.1(ANKRD31):c.2388T>G (p.Asp796Glu)	ANKRD31 (D796E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229008	NM_001372053.1(ANKRD31):c.2369G>A (p.Ser790Asn)	ANKRD31 (S790N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457936	NM_001372053.1(ANKRD31):c.2318A>C (p.His773Pro)	ANKRD31 (H773P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289569	NM_001372053.1(ANKRD31):c.2184A>G (p.Ile728Met)	ANKRD31 (I728M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599837	NM_001372053.1(ANKRD31):c.2177A>C (p.Lys726Thr)	ANKRD31 (K726T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368579	NM_001372053.1(ANKRD31):c.2173C>T (p.Pro725Ser)	ANKRD31 (P725S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2401534	NM_001372053.1(ANKRD31):c.2125C>T (p.Leu709Phe)	ANKRD31 (L709F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398055	NM_001372053.1(ANKRD31):c.2123G>A (p.Gly708Glu)	ANKRD31 (G708E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208926	NM_001372053.1(ANKRD31):c.2112A>G (p.Ile704Met)	ANKRD31 (I704M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328614	NM_001372053.1(ANKRD31):c.2066C>T (p.Thr689Ile)	ANKRD31 (T689I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396861	NM_001372053.1(ANKRD31):c.2059A>C (p.Lys687Gln)	ANKRD31 (K687Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2220338	NM_001372053.1(ANKRD31):c.2033T>C (p.Val678Ala)	ANKRD31 (V678A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125361	NM_001372053.1(ANKRD31):c.2018T>C (p.Ile673Thr)	ANKRD31 (I673T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555894	NM_001372053.1(ANKRD31):c.2005G>A (p.Ala669Thr)	ANKRD31 (A669T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125357	NM_001372053.1(ANKRD31):c.1997G>T (p.Gly666Val)	ANKRD31 (G666V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299170	NM_001372053.1(ANKRD31):c.1960A>T (p.Asn654Tyr)	ANKRD31 (N654Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460590	NM_001372053.1(ANKRD31):c.1919G>T (p.Ser640Ile)	ANKRD31 (S640I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406170	NM_001372053.1(ANKRD31):c.1865G>A (p.Ser622Asn)	ANKRD31 (S622N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250745	NM_001372053.1(ANKRD31):c.1841G>A (p.Cys614Tyr)	ANKRD31 (C614Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125348	NM_001372053.1(ANKRD31):c.1795T>C (p.Cys599Arg)	ANKRD31 (C599R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3297370	NM_001372053.1(ANKRD31):c.1760A>G (p.Asp587Gly)	ANKRD31 (D587G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125345	NM_001372053.1(ANKRD31):c.1696G>A (p.Gly566Arg)	ANKRD31 (G566R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343105	NM_001372053.1(ANKRD31):c.1694A>G (p.Asn565Ser)	ANKRD31 (N565S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297366	NM_001372053.1(ANKRD31):c.1687G>A (p.Val563Met)	ANKRD31 (V563M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 714297	NM_001372053.1(ANKRD31):c.1669A>G (p.Thr557Ala)	ANKRD31 (T557A)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1120014	NM_001372053.1(ANKRD31):c.1565-2A>G	ANKRD31	Single nucleotide variant (splice acceptor variant)	Genetic non-acquired premature ovarian failure	GPathogenic
Select item 2410397	NM_001372053.1(ANKRD31):c.1542T>G (p.Asn514Lys)	ANKRD31 (N514K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480431	NM_001372053.1(ANKRD31):c.1495C>T (p.His499Tyr)	ANKRD31 (H499Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229660	NM_001372053.1(ANKRD31):c.1450C>T (p.Arg484Trp)	ANKRD31 (R484W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481268	NM_001372053.1(ANKRD31):c.1429A>G (p.Ile477Val)	ANKRD31 (I477V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407981	NM_001372053.1(ANKRD31):c.1420G>A (p.Val474Met)	ANKRD31 (V474M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2367879	NM_001372053.1(ANKRD31):c.1261G>A (p.Asp421Asn)	ANKRD31 (D421N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 2