"Ambry Genetics"[submitter] AND "SVIL"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2215311	NM_021738.3(SVIL):c.6602C>T (p.Ala2201Val)	SVIL, SVIL-AS1 (A1891V +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3172474	NM_021738.3(SVIL):c.6601G>A (p.Ala2201Thr)	SVIL, SVIL-AS1 (A1775T +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2324076	NM_021738.3(SVIL):c.6560T>C (p.Phe2187Ser)	SVIL, SVIL-AS1 (F1761S +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3172473	NM_021738.3(SVIL):c.6556G>A (p.Glu2186Lys)	SVIL, SVIL-AS1 (E1792K +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2209505	NM_021738.3(SVIL):c.6544G>A (p.Asp2182Asn)	SVIL, SVIL-AS1 (D1756N +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2490421	NM_021738.3(SVIL):c.6506A>C (p.Glu2169Ala)	SVIL, SVIL-AS1 (E1775A +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2259646	NM_021738.3(SVIL):c.6484C>T (p.Leu2162Phe)	SVIL, SVIL-AS1 (L1736F +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3172471	NM_021738.3(SVIL):c.6481G>A (p.Asp2161Asn)	SVIL, SVIL-AS1 (D1851N +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3172470	NM_021738.3(SVIL):c.6448G>A (p.Ala2150Thr)	SVIL, SVIL-AS1 (A1756T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323762	NM_021738.3(SVIL):c.6419A>G (p.Asn2140Ser)	SVIL, SVIL-AS1 (N1714S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526696	NM_021738.3(SVIL):c.6353T>C (p.Met2118Thr)	SVIL, SVIL-AS1 (M1808T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172469	NM_021738.3(SVIL):c.6347C>T (p.Thr2116Ile)	SVIL, SVIL-AS1 (T1806I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380019	NM_021738.3(SVIL):c.6301C>A (p.Pro2101Thr)	SVIL, SVIL-AS1 (P1675T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557493	NM_021738.3(SVIL):c.6286C>G (p.Leu2096Val)	SVIL, SVIL-AS1 (L2096V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172468	NM_021738.3(SVIL):c.6223C>T (p.Arg2075Cys)	SVIL, SVIL-AS1 (R1765C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486748	NM_021738.3(SVIL):c.6169C>T (p.Leu2057Phe)	SVIL, SVIL-AS1 (L1747F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267539	NM_021738.3(SVIL):c.6163G>A (p.Val2055Met)	SVIL, SVIL-AS1 (V2055M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323760	NM_021738.3(SVIL):c.6068G>A (p.Arg2023Gln)	SVIL, SVIL-AS1 (R1713Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204672	NM_021738.3(SVIL):c.6034G>A (p.Asp2012Asn)	SVIL, SVIL-AS1 (D1618N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230442	NM_021738.3(SVIL):c.5998G>C (p.Ala2000Pro)	SVIL, SVIL-AS1 (A1690P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323763	NM_021738.3(SVIL):c.5970G>A (p.Met1990Ile)	SVIL, SVIL-AS1 (M1564I +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2525706	NM_021738.3(SVIL):c.5893G>A (p.Glu1965Lys)	SVIL, SVIL-AS1 (E1571K +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2495706	NM_021738.3(SVIL):c.5858C>G (p.Ala1953Gly)	SVIL, SVIL-AS1 (A1527G +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3172467	NM_021738.3(SVIL):c.5821G>A (p.Ala1941Thr)	SVIL, SVIL-AS1 (A1515T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508625	NM_021738.3(SVIL):c.5749G>A (p.Val1917Ile)	SVIL, SVIL-AS1 (V1607I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278488	NM_021738.3(SVIL):c.5714G>A (p.Ser1905Asn)	SVIL, SVIL-AS1 (S1479N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486518	NM_021738.3(SVIL):c.5696T>G (p.Val1899Gly)	SVIL, SVIL-AS1 (V1899G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553321	NM_021738.3(SVIL):c.5666A>G (p.Glu1889Gly)	SVIL, SVIL-AS1 (E1463G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172466	NM_021738.3(SVIL):c.5660G>A (p.Arg1887His)	SVIL, SVIL-AS1 (R1887H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323766	NM_021738.3(SVIL):c.5630T>G (p.Val1877Gly)	SVIL, SVIL-AS1 (V1567G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555926	NM_021738.3(SVIL):c.5596C>A (p.His1866Asn)	SVIL, SVIL-AS1 (H1556N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246779	NM_021738.3(SVIL):c.5581G>A (p.Gly1861Arg)	SVIL, SVIL-AS1 (G1467R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368644	NM_021738.3(SVIL):c.5498C>T (p.Thr1833Met)	SVIL, SVIL-AS1 (T1833M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172465	NM_021738.3(SVIL):c.5495T>C (p.Met1832Thr)	SVIL, SVIL-AS1 (M1438T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172464	NM_021738.3(SVIL):c.5483C>T (p.Thr1828Met)	SVIL, SVIL-AS1 (T1402M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243130	NM_021738.3(SVIL):c.5456G>A (p.Arg1819Gln)	SVIL, SVIL-AS1 (R1393Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521493	NM_021738.3(SVIL):c.5455C>T (p.Arg1819Trp)	SVIL, SVIL-AS1 (R1819W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594141	NM_021738.3(SVIL):c.5419G>A (p.Gly1807Ser)	SVIL, SVIL-AS1 (G1497S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218149	NM_021738.3(SVIL):c.5407G>A (p.Val1803Met)	SVIL, SVIL-AS1 (V1409M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383108	NM_021738.3(SVIL):c.5395G>A (p.Gly1799Arg)	SVIL, SVIL-AS1 (G1799R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285607	NM_021738.3(SVIL):c.5391G>C (p.Gln1797His)	SVIL, SVIL-AS1 (Q1487H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172463	NM_021738.3(SVIL):c.5386C>G (p.Arg1796Gly)	SVIL, SVIL-AS1 (R1796G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172462	NM_021738.3(SVIL):c.5362A>G (p.Met1788Val)	SVIL, SVIL-AS1 (M1362V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238238	NM_021738.3(SVIL):c.5299C>T (p.Leu1767Phe)	SVIL, SVIL-AS1 (L1341F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208012	NM_021738.3(SVIL):c.5260G>A (p.Val1754Met)	SVIL, SVIL-AS1 (V1328M +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2316691	NM_021738.3(SVIL):c.5197G>A (p.Gly1733Ser)	SVIL, SVIL-AS1 (G1339S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410858	NM_021738.3(SVIL):c.5194G>A (p.Val1732Ile)	SVIL, SVIL-AS1 (V1732I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482653	NM_021738.3(SVIL):c.5192A>T (p.Asn1731Ile)	SVIL, SVIL-AS1 (N1337I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204317	NM_021738.3(SVIL):c.5162C>T (p.Thr1721Met)	SVIL, SVIL-AS1 (T1327M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386898	NM_021738.3(SVIL):c.5140C>T (p.Arg1714Trp)	SVIL, SVIL-AS1 (R1714W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355590	NM_021738.3(SVIL):c.5077C>T (p.Pro1693Ser)	SVIL, SVIL-AS1 (P1383S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172460	NM_021738.3(SVIL):c.4999A>C (p.Thr1667Pro)	SVIL, SVIL-AS1 (T1273P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172459	NM_021738.3(SVIL):c.4928C>T (p.Pro1643Leu)	SVIL, SVIL-AS1 (P1333L +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2384542	NM_021738.3(SVIL):c.4912A>G (p.Ile1638Val)	SVIL, SVIL-AS1 (I1212V +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2381076	NM_021738.3(SVIL):c.4813G>C (p.Val1605Leu)	SVIL, SVIL-AS1 (V1211L +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2379379	NM_021738.3(SVIL):c.4813G>A (p.Val1605Ile)	SVIL, SVIL-AS1 (V1211I +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3172457	NM_021738.3(SVIL):c.4544A>G (p.Tyr1515Cys)	SVIL, SVIL-AS1 (Y1089C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367739	NM_021738.3(SVIL):c.4501A>G (p.Thr1501Ala)	SVIL, SVIL-AS1 (T1107A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172456	NM_021738.3(SVIL):c.4495C>A (p.Leu1499Ile)	SVIL, SVIL-AS1 (L1189I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211033	NM_021738.3(SVIL):c.4312G>A (p.Val1438Met)	SVIL (V1128M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371386	NM_021738.3(SVIL):c.4270C>T (p.Arg1424Trp)	SVIL (R1030W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602230	NM_021738.3(SVIL):c.4205C>T (p.Ser1402Phe)	SVIL (S1402F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342661	NM_021738.3(SVIL):c.4142A>G (p.Gln1381Arg)	SVIL (Q987R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172454	NM_021738.3(SVIL):c.4070G>A (p.Arg1357Gln)	SVIL (R1047Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172453	NM_021738.3(SVIL):c.4066C>T (p.Arg1356Cys)	SVIL (R930C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172452	NM_021738.3(SVIL):c.4055T>C (p.Val1352Ala)	SVIL (V926A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370079	NM_021738.3(SVIL):c.4052C>A (p.Ala1351Glu)	SVIL (A957E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323767	NM_021738.3(SVIL):c.3956T>G (p.Met1319Arg)	SVIL (M1319R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172451	NM_021738.3(SVIL):c.3946G>T (p.Asp1316Tyr)	SVIL (D922Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172450	NM_021738.3(SVIL):c.3860C>T (p.Thr1287Met)	SVIL (T977M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517637	NM_021738.3(SVIL):c.3855C>G (p.His1285Gln)	SVIL (H891Q +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2591276	NM_021738.3(SVIL):c.3814A>T (p.Thr1272Ser)	SVIL (T878S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323768	NM_021738.3(SVIL):c.3770C>T (p.Pro1257Leu)	SVIL (P1257L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532298	NM_021738.3(SVIL):c.3745C>A (p.Pro1249Thr)	SVIL (P823T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172448	NM_021738.3(SVIL):c.3710G>A (p.Cys1237Tyr)	SVIL (C811Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323761	NM_021738.3(SVIL):c.3622G>A (p.Asp1208Asn)	SVIL (D1208N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343247	NM_021738.3(SVIL):c.3619A>G (p.Asn1207Asp)	SVIL (N781D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260158	NM_021738.3(SVIL):c.3617C>T (p.Ala1206Val)	SVIL (A812V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172446	NM_021738.3(SVIL):c.3614C>T (p.Ala1205Val)	SVIL (A1205V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379377	NM_021738.3(SVIL):c.3530G>C (p.Ser1177Thr)	SVIL (S1177T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622435	NM_021738.3(SVIL):c.3477C>G (p.Ser1159Arg)	SVIL (S765R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602815	NM_021738.3(SVIL):c.3322G>A (p.Glu1108Lys)	SVIL (E1108K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268773	NM_021738.3(SVIL):c.3268G>C (p.Glu1090Gln)	SVIL (E1090Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172445	NM_021738.3(SVIL):c.3190G>A (p.Glu1064Lys)	SVIL (E1064K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616437	NM_021738.3(SVIL):c.3187T>G (p.Ser1063Ala)	SVIL (S637A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548661	NM_021738.3(SVIL):c.3060G>A (p.Met1020Ile)	SVIL (M594I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303496	NM_021738.3(SVIL):c.3034G>A (p.Gly1012Arg)	SVIL (G586R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393555	NM_021738.3(SVIL):c.3032T>G (p.Leu1011Arg)	SVIL (L617R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399529	NM_021738.3(SVIL):c.3031C>G (p.Leu1011Val)	SVIL (L701V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172443	NM_021738.3(SVIL):c.3026C>T (p.Thr1009Ile)	SVIL (T615I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535193	NM_021738.3(SVIL):c.3008G>A (p.Arg1003Gln)	SVIL (R1003Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358263	NM_021738.3(SVIL):c.2909A>T (p.Glu970Val)	SVIL (E970V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172440	NM_021738.3(SVIL):c.2846A>G (p.Glu949Gly)	SVIL (E949G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172439	NM_021738.3(SVIL):c.2809G>A (p.Gly937Ser)	SVIL (G627S +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2514602	NM_021738.3(SVIL):c.2804T>C (p.Val935Ala)	SVIL (V625A +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3172438	NM_021738.3(SVIL):c.2783C>T (p.Ser928Leu)	SVIL (S928L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355863	NM_021738.3(SVIL):c.2771G>A (p.Ser924Asn)	SVIL (S530N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408725	NM_021738.3(SVIL):c.2674G>A (p.Gly892Arg)	SVIL (G466R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172437	NM_021738.3(SVIL):c.2665A>G (p.Met889Val)	SVIL (M889V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400252	NM_021738.3(SVIL):c.2623G>A (p.Val875Met)	SVIL (V481M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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