"Ambry Genetics"[submitter] AND "LMF2"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2314224	NM_033200.3(LMF2):c.2120A>G (p.Lys707Arg)	LMF2 (K682R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330007	NM_033200.3(LMF2):c.2116A>C (p.Lys706Gln)	LMF2 (K681Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511902	NM_033200.3(LMF2):c.2114G>A (p.Arg705Gln)	LMF2 (R680Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216978	NM_033200.3(LMF2):c.2110C>T (p.Arg704Trp)	LMF2 (R679W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289925	NM_033200.3(LMF2):c.2108C>A (p.Thr703Asn)	LMF2 (T703N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478060	NM_033200.3(LMF2):c.2104A>C (p.Thr702Pro)	LMF2 (T702P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458754	NM_033200.3(LMF2):c.2092A>G (p.Ser698Gly)	LMF2 (S698G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592927	NM_033200.3(LMF2):c.2071G>A (p.Ala691Thr)	LMF2 (A666T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278565	NM_033200.3(LMF2):c.2047G>A (p.Gly683Arg)	LMF2 (G658R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2388080	NM_033200.3(LMF2):c.2027C>T (p.Pro676Leu)	LMF2 (P651L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252428	NM_033200.3(LMF2):c.2021G>T (p.Arg674Leu)	LMF2 (R649L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204237	NM_033200.3(LMF2):c.2015A>G (p.Glu672Gly)	LMF2 (E647G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521100	NM_033200.3(LMF2):c.2011G>A (p.Gly671Arg)	LMF2 (G646R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119286	NM_033200.3(LMF2):c.2003C>T (p.Pro668Leu)	LMF2 (P643L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2230616	NM_033200.3(LMF2):c.1994C>T (p.Pro665Leu)	LMF2 (P640L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602175	NM_033200.3(LMF2):c.1985G>A (p.Arg662Gln)	LMF2 (R662Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2231457	NM_033200.3(LMF2):c.1940G>A (p.Gly647Glu)	LMF2 (G647E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119285	NM_033200.3(LMF2):c.1931T>A (p.Met644Lys)	LMF2 (M619K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340340	NM_033200.3(LMF2):c.1918T>C (p.Trp640Arg)	LMF2 (W640R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209378	NM_033200.3(LMF2):c.1909G>A (p.Ala637Thr)	LMF2 (A637T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3119284	NM_033200.3(LMF2):c.1897C>G (p.Leu633Val)	LMF2 (L608V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621685	NM_033200.3(LMF2):c.1894C>A (p.Pro632Thr)	LMF2 (P607T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391143	NM_033200.3(LMF2):c.1838G>A (p.Arg613His)	LMF2 (R613H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211267	NM_033200.3(LMF2):c.1837C>T (p.Arg613Cys)	LMF2 (R613C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119283	NM_033200.3(LMF2):c.1795C>T (p.Leu599Phe)	LMF2 (L599F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284892	NM_033200.3(LMF2):c.1781C>T (p.Thr594Met)	LMF2 (T594M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119282	NM_033200.3(LMF2):c.1762G>C (p.Val588Leu)	LMF2 (V563L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352487	NM_033200.3(LMF2):c.1756C>T (p.Pro586Ser)	LMF2 (P586S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119281	NM_033200.3(LMF2):c.1730G>A (p.Arg577Gln)	LMF2 (R577Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356048	NM_033200.3(LMF2):c.1730G>T (p.Arg577Leu)	LMF2 (R577L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119280	NM_033200.3(LMF2):c.1712A>G (p.Glu571Gly)	LMF2 (E571G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119279	NM_033200.3(LMF2):c.1685A>G (p.Tyr562Cys)	LMF2 (Y562C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119278	NM_033200.3(LMF2):c.1682G>A (p.Arg561His)	LMF2 (R561H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591175	NM_033200.3(LMF2):c.1673G>A (p.Arg558Gln)	LMF2 (R558Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119277	NM_033200.3(LMF2):c.1649A>C (p.His550Pro)	LMF2 (H550P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468337	NM_033200.3(LMF2):c.1648C>A (p.His550Asn)	LMF2 (H525N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368535	NM_033200.3(LMF2):c.1648C>T (p.His550Tyr)	LMF2 (H550Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290952	NM_033200.3(LMF2):c.1643C>G (p.Pro548Arg)	LMF2 (P523R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467833	NM_033200.3(LMF2):c.1625G>T (p.Ser542Ile)	LMF2 (S517I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290947	NM_033200.3(LMF2):c.1603C>T (p.Pro535Ser)	LMF2 (P535S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290950	NM_033200.3(LMF2):c.1602G>T (p.Glu534Asp)	LMF2 (E509D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290953	NM_033200.3(LMF2):c.1585C>A (p.Leu529Met)	LMF2 (L529M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463080	NM_033200.3(LMF2):c.1571G>C (p.Ser524Thr)	LMF2 (S499T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358369	NM_033200.3(LMF2):c.1550C>T (p.Thr517Met)	LMF2 (T492M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119275	NM_033200.3(LMF2):c.1508G>A (p.Arg503His)	LMF2 (R503H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119274	NM_033200.3(LMF2):c.1504C>T (p.Pro502Ser)	LMF2 (P502S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290951	NM_033200.3(LMF2):c.1498C>T (p.His500Tyr)	LMF2 (H475Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378318	NM_033200.3(LMF2):c.1495C>T (p.Pro499Ser)	LMF2 (P474S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213863	NM_033200.3(LMF2):c.1493T>C (p.Val498Ala)	LMF2 (V498A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3119273	NM_033200.3(LMF2):c.1489G>A (p.Val497Met)	LMF2 (V472M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467045	NM_033200.3(LMF2):c.1484C>T (p.Pro495Leu)	LMF2 (P495L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376308	NM_033200.3(LMF2):c.1475G>A (p.Arg492Gln)	LMF2 (R492Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370666	NM_033200.3(LMF2):c.1423G>A (p.Gly475Ser)	LMF2 (G475S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290949	NM_033200.3(LMF2):c.1306G>A (p.Ala436Thr)	LMF2 (A436T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613825	NM_033200.3(LMF2):c.1297T>C (p.Trp433Arg)	LMF2 (W433R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331629	NM_033200.3(LMF2):c.1279G>A (p.Gly427Arg)	LMF2 (G402R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336290	NM_033200.3(LMF2):c.1270G>A (p.Val424Met)	LMF2 (V399M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2406759	NM_033200.3(LMF2):c.1231G>A (p.Val411Met)	LMF2 (V386M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403835	NM_033200.3(LMF2):c.1226C>T (p.Ala409Val)	LMF2 (A384V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119272	NM_033200.3(LMF2):c.1213C>T (p.Leu405Phe)	LMF2 (L380F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290944	NM_033200.3(LMF2):c.1184G>A (p.Arg395Gln)	LMF2 (R370Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2226640	NM_033200.3(LMF2):c.1172G>A (p.Arg391Gln)	LMF2 (R391Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3119271	NM_033200.3(LMF2):c.1031G>A (p.Arg344His)	LMF2 (R319H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2478372	NM_033200.3(LMF2):c.1030C>T (p.Arg344Cys)	LMF2 (R344C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119270	NM_033200.3(LMF2):c.1015G>A (p.Val339Ile)	LMF2 (V314I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511780	NM_033200.3(LMF2):c.973G>A (p.Gly325Arg)	LMF2 (G325R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119296	NM_033200.3(LMF2):c.932T>G (p.Leu311Arg)	LMF2 (L286R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290946	NM_033200.3(LMF2):c.908C>T (p.Thr303Met)	LMF2 (T303M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119295	NM_033200.3(LMF2):c.898C>T (p.Arg300Cys)	LMF2 (R300C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119294	NM_033200.3(LMF2):c.887G>T (p.Gly296Val)	LMF2 (G271V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381202	NM_033200.3(LMF2):c.882G>T (p.Glu294Asp)	LMF2 (E294D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290948	NM_033200.3(LMF2):c.868C>T (p.His290Tyr)	LMF2 (H290Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119293	NM_033200.3(LMF2):c.864C>G (p.Asp288Glu)	LMF2 (D263E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388729	NM_033200.3(LMF2):c.862G>A (p.Asp288Asn)	LMF2 (D288N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119292	NM_033200.3(LMF2):c.831G>A (p.Met277Ile)	LMF2 (M252I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538981	NM_033200.3(LMF2):c.824A>C (p.Asn275Thr)	LMF2 (N250T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346361	NM_033200.3(LMF2):c.758C>T (p.Ala253Val)	LMF2 (A228V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240160	NM_033200.3(LMF2):c.752G>A (p.Arg251His)	LMF2 (R251H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321757	NM_033200.3(LMF2):c.733G>A (p.Ala245Thr)	LMF2 (A220T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239093	NM_033200.3(LMF2):c.707A>G (p.Glu236Gly)	LMF2 (E211G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464667	NM_033200.3(LMF2):c.637G>A (p.Ala213Thr)	LMF2 (A213T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589662	NM_033200.3(LMF2):c.613G>C (p.Glu205Gln)	LMF2 (E205Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623790	NM_033200.3(LMF2):c.609C>G (p.His203Gln)	LMF2 (H203Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316578	NM_033200.3(LMF2):c.566G>C (p.Ser189Thr)	LMF2 (S164T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315209	NM_033200.3(LMF2):c.532C>T (p.Leu178Phe)	LMF2 (L153F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351023	NM_033200.3(LMF2):c.529C>T (p.Arg177Cys)	LMF2 (R152C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466321	NM_033200.3(LMF2):c.515G>A (p.Arg172Gln)	LMF2 (R172Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373394	NM_033200.3(LMF2):c.479C>A (p.Ala160Asp)	LMF2 (A135D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353685	NM_033200.3(LMF2):c.469C>A (p.Gln157Lys)	LMF2 (Q157K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213627	NM_033200.3(LMF2):c.455C>T (p.Ala152Val)	LMF2 (A127V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119288	NM_033200.3(LMF2):c.445C>T (p.Arg149Cys)	LMF2 (R149C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476976	NM_033200.3(LMF2):c.311A>G (p.Tyr104Cys)	LMF2 (Y104C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321154	NM_033200.3(LMF2):c.296G>A (p.Arg99His)	LMF2 (R99H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260505	NM_033200.3(LMF2):c.289C>T (p.Pro97Ser)	LMF2 (P97S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459540	NM_033200.3(LMF2):c.256G>A (p.Ala86Thr)	LMF2 (A86T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3119287	NM_033200.3(LMF2):c.227A>G (p.Gln76Arg)	LMF2 (Q76R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119291	NM_033200.3(LMF2):c.74C>T (p.Ser25Phe)	LMF2 (S25F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3119289	NM_033200.3(LMF2):c.50C>G (p.Ala17Gly)	LMF2 (A17G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2468051	NM_033200.3(LMF2):c.40G>A (p.Gly14Ser)	LMF2 (G14S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2615569	NM_033200.3(LMF2):c.22C>T (p.Arg8Trp)	LMF2 (R8W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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