ClinVar for Gene (Select 4233) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3371949	NM_000245.4(MET):c.2566A>T (p.Asn856Tyr)	MET (N426Y +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3369459	NM_000245.4(MET):c.3037C>T (p.Pro1013Ser)	MET (P1013S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368854	NM_000245.4(MET):c.3781A>G (p.Thr1261Ala)	MET (T1261A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367473	NM_000245.4(MET):c.2265-50T>C	MET (W757R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3367230	NM_000245.4(MET):c.2797G>A (p.Gly933Arg)	MET (G503R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3364678	NM_000245.4(MET):c.490C>T (p.Pro164Ser)	MET (P164S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3364305	NM_000245.4(MET):c.2599C>T (p.Pro867Ser)	MET (P437S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3363493	NM_000245.4(MET):c.2359A>T (p.Thr787Ser)	MET (T357S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3359619	NM_000245.4(MET):c.3205G>A (p.Val1069Ile)	MET (V1069I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3347915	NM_000245.4(MET):c.1196del (p.Asn399fs)	MET (N399fs)	Deletion (frameshift variant +1 more)	MET-related disorder	GUncertain significance
Select item 3346767	NM_000245.4(MET):c.1966-6C>T	MET	Single nucleotide variant (intron variant)	MET-related disorder	GLikely benign
Select item 3344636	NM_000245.4(MET):c.1389G>T (p.Met463Ile)	MET (M33I +1 more)	Single nucleotide variant (missense variant)	MET-related disorder	GUncertain significance
Select item 3344602	NM_000245.4(MET):c.2471A>C (p.Asp824Ala)	MET (D394A +2 more)	Single nucleotide variant (missense variant)	MET-related disorder	GUncertain significance
Select item 3343069	NM_000245.4(MET):c.3818T>C (p.Leu1273Pro)	MET (L1273P +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3294392	NM_000245.4(MET):c.4096C>G (p.Pro1366Ala)	MET (P936A +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294391	NM_000245.4(MET):c.1475T>C (p.Val492Ala)	MET (V62A +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294390	NM_000245.4(MET):c.953A>G (p.Gln318Arg)	MET (Q318R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294389	NM_000245.4(MET):c.3492T>G (p.Asp1164Glu)	MET (D1164E +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294388	NM_000245.4(MET):c.2605G>A (p.Ala869Thr)	MET (A439T +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294387	NM_000245.4(MET):c.2021T>C (p.Leu674Ser)	MET (L244S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294386	NM_000245.4(MET):c.1031G>A (p.Gly344Glu)	MET (G344E)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294385	NM_000245.4(MET):c.3455C>T (p.Ser1152Phe)	MET (S1152F +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294384	NM_000245.4(MET):c.3843C>G (p.Ala1281=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294382	NM_000245.4(MET):c.3601G>C (p.Val1201Leu)	MET (V771L +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294381	NM_000245.4(MET):c.1291A>T (p.Met431Leu)	MET (M431L +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294380	NM_000245.4(MET):c.3237T>C (p.His1079=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294379	NM_000245.4(MET):c.773T>C (p.Phe258Ser)	MET (F258S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294378	NM_000245.4(MET):c.2957C>T (p.Ala986Val)	MET (A1004V +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294377	NM_000245.4(MET):c.2838A>G (p.Leu946=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294376	NM_000245.4(MET):c.952C>G (p.Gln318Glu)	MET (Q318E)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294374	NM_000245.4(MET):c.2260A>T (p.Ile754Phe)	MET (I754F +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294373	NM_000245.4(MET):c.2265-47T>C	MET (W758R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294372	NM_000245.4(MET):c.514T>G (p.Cys172Gly)	MET (C172G)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294371	NM_000245.4(MET):c.3455C>A (p.Ser1152Tyr)	MET (S1152Y +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294370	NM_000245.4(MET):c.1678A>C (p.Ile560Leu)	MET (I130L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294369	NM_000245.4(MET):c.2619A>C (p.Glu873Asp)	MET (E443D +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294368	NM_000245.4(MET):c.4000G>C (p.Val1334Leu)	MET (V1334L +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294366	NM_000245.4(MET):c.4111T>A (p.Ser1371Thr)	MET (S1371T +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294365	NM_000245.4(MET):c.4111T>C (p.Ser1371Pro)	MET (S941P +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294364	NM_000245.4(MET):c.1506A>C (p.Thr502=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294363	NM_000245.4(MET):c.2195A>G (p.Glu732Gly)	MET (E302G +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294362	NM_000245.4(MET):c.2336T>A (p.Val779Glu)	MET (V779E +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294361	NM_000245.4(MET):c.2893G>C (p.Gly965Arg)	MET (G535R +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294358	NM_000245.4(MET):c.3714C>A (p.His1238Gln)	MET (H1238Q +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294357	NM_000245.4(MET):c.4173G>A (p.Ter1391=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294356	NM_000245.4(MET):c.1460C>T (p.Ser487Phe)	MET (S487F +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294355	NM_000245.4(MET):c.962A>C (p.Tyr321Ser)	MET (Y321S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294354	NM_000245.4(MET):c.1831A>C (p.Thr611Pro)	MET (T181P +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294353	NM_000245.4(MET):c.2963G>T (p.Ser988Ile)	MET (S558I +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294352	NM_000245.4(MET):c.2846T>G (p.Leu949Arg)	MET (L949R +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294351	NM_000245.4(MET):c.2102+1G>C	MET	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294350	NM_000245.4(MET):c.1400T>A (p.Val467Asp)	MET (V37D +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294348	NM_000245.4(MET):c.1883C>T (p.Pro628Leu)	MET (P628L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294347	NM_000245.4(MET):c.2039A>G (p.Asn680Ser)	MET (N250S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294346	NM_000245.4(MET):c.1689T>G (p.Pro563=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294345	NM_000245.4(MET):c.655C>T (p.Leu219=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294344	NM_000245.4(MET):c.2223T>C (p.Asp741=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294343	NM_000245.4(MET):c.1143C>A (p.Asn381Lys)	MET (N381K)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294342	NM_000245.4(MET):c.1137C>A (p.Asn379Lys)	MET (N379K)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294341	NM_000245.4(MET):c.974C>A (p.Pro325His)	MET (P325H)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294340	NM_000245.4(MET):c.1606G>A (p.Val536Ile)	MET (V106I +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294339	NM_000245.4(MET):c.434T>A (p.Val145Asp)	MET (V145D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294338	NM_000245.4(MET):c.396C>G (p.Ser132Arg)	MET (S132R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294337	NM_000245.4(MET):c.1471A>C (p.Ile491Leu)	MET (I61L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294336	NM_000245.4(MET):c.2816T>G (p.Val939Gly)	MET (V957G +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294335	NM_000245.4(MET):c.1413A>G (p.Gly471=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294334	NM_000245.4(MET):c.547A>G (p.Lys183Glu)	MET (K183E)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294333	NM_000245.4(MET):c.3269G>C (p.Gly1090Ala)	MET (G1090A +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294332	NM_000245.4(MET):c.3260G>A (p.Gly1087Glu)	MET (G657E +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294330	NM_000245.4(MET):c.3533T>C (p.Val1178Ala)	MET (V1178A +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294329	NM_000245.4(MET):c.1930C>T (p.His644Tyr)	MET (H214Y +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294328	NM_000245.4(MET):c.1422C>G (p.Thr474=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294327	NM_000245.4(MET):c.2167A>T (p.Lys723Ter)	MET (K723* +1 more)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294326	NM_000245.4(MET):c.2118T>G (p.Ile706Met)	MET (I276M +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294325	NM_000245.4(MET):c.2494G>C (p.Asp832His)	MET (D832H +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294324	NM_000245.4(MET):c.438T>C (p.Phe146=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294323	NM_000245.4(MET):c.3072G>T (p.Val1024=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294322	NM_000245.4(MET):c.1949G>A (p.Ser650Asn)	MET (S220N +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294321	NM_000245.4(MET):c.1948A>C (p.Ser650Arg)	MET (S220R +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294320	NM_000245.4(MET):c.1948_1949delinsCA (p.Ser650His)	MET (S220H +1 more)	Indel (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294319	NM_000245.4(MET):c.2364+1G>T	MET	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294318	NM_000245.4(MET):c.1268C>T (p.Ala423Val)	MET (A423V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294317	NM_000245.4(MET):c.2334T>A (p.Asn778Lys)	MET (N778K +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294316	NM_000245.4(MET):c.103A>G (p.Met35Val)	MET (M35V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294315	NM_000245.4(MET):c.1619G>A (p.Trp540Ter)	MET (W110* +1 more)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294314	NM_000245.4(MET):c.3627C>T (p.Asn1209=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294313	NM_000245.4(MET):c.1144A>G (p.Asn382Asp)	MET (N382D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294312	NM_000245.4(MET):c.2465T>G (p.Met822Arg)	MET (M822R +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294311	NM_000245.4(MET):c.3761G>A (p.Ser1254Asn)	MET (S1254N +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294310	NM_000245.4(MET):c.2183T>C (p.Leu728Ser)	MET (L298S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294309	NM_000245.4(MET):c.2654T>C (p.Ile885Thr)	MET (I455T +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294308	NM_000245.4(MET):c.3010C>T (p.Arg1004Ter)	MET (R574* +2 more)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294306	NM_000245.4(MET):c.88C>G (p.Leu30Val)	MET (L30V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294304	NM_000245.4(MET):c.365T>G (p.Val122Gly)	MET (V122G)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294303	NM_000245.4(MET):c.2265-8T>C	MET (F771L)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294301	NM_000245.4(MET):c.54G>T (p.Leu18Phe)	MET (L18F)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3294299	NM_000245.4(MET):c.3849T>G (p.Pro1283=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294297	NM_000245.4(MET):c.3207A>G (p.Val1069=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294296	NM_000245.4(MET):c.3033G>A (p.Gln1011=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3294295	NM_000245.4(MET):c.2683A>G (p.Thr895Ala)	MET (T465A +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance

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