"Ambry Genetics"[submitter] AND "MYOM2"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3168608	NM_003970.4(MYOM2):c.35G>A (p.Arg12Lys)	MYOM2 (R12K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391936	NM_003970.4(MYOM2):c.61C>T (p.Arg21Cys)	MYOM2 (R21C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168740	NM_003970.4(MYOM2):c.76C>T (p.Arg26Trp)	MYOM2 (R26W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168348	NM_003970.4(MYOM2):c.152G>A (p.Arg51Gln)	MYOM2 (R51Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168395	NM_003970.4(MYOM2):c.212G>T (p.Cys71Phe)	MYOM2 (C71F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568579	NM_003970.4(MYOM2):c.319G>A (p.Glu107Lys)	MYOM2 (E107K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388369	NM_003970.4(MYOM2):c.368G>A (p.Arg123His)	MYOM2 (R123H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530437	NM_003970.4(MYOM2):c.425A>G (p.Glu142Gly)	MYOM2 (E142G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399313	NM_003970.4(MYOM2):c.442G>A (p.Glu148Lys)	MYOM2 (E148K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532078	NM_003970.4(MYOM2):c.529G>A (p.Val177Met)	MYOM2 (V177M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246861	NM_003970.4(MYOM2):c.541C>G (p.Pro181Ala)	MYOM2 (P181A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168708	NM_003970.4(MYOM2):c.561G>T (p.Trp187Cys)	MYOM2 (W187C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463233	NM_003970.4(MYOM2):c.631G>A (p.Val211Ile)	MYOM2 (V211I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168720	NM_003970.4(MYOM2):c.640C>G (p.Leu214Val)	MYOM2 (L214V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168724	NM_003970.4(MYOM2):c.686C>T (p.Ala229Val)	MYOM2 (A229V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254031	NM_003970.4(MYOM2):c.715T>G (p.Ser239Ala)	MYOM2 (S239A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522178	NM_003970.4(MYOM2):c.728C>T (p.Ala243Val)	MYOM2 (A243V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168731	NM_003970.4(MYOM2):c.734T>C (p.Val245Ala)	MYOM2 (V245A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351309	NM_003970.4(MYOM2):c.748C>T (p.Arg250Trp)	MYOM2 (R250W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310399	NM_003970.4(MYOM2):c.821C>A (p.Thr274Lys)	MYOM2 (T274K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615884	NM_003970.4(MYOM2):c.875G>A (p.Gly292Asp)	MYOM2 (G292D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209170	NM_003970.4(MYOM2):c.948G>T (p.Trp316Cys)	MYOM2 (W316C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168751	NM_003970.4(MYOM2):c.986C>T (p.Thr329Met)	MYOM2 (T329M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287333	NM_003970.4(MYOM2):c.1011G>C (p.Gln337His)	MYOM2 (Q337H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404300	NM_003970.4(MYOM2):c.1024T>C (p.Phe342Leu)	MYOM2 (F342L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457226	NM_003970.4(MYOM2):c.1041G>T (p.Lys347Asn)	MYOM2 (K347N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337639	NM_003970.4(MYOM2):c.1054C>G (p.Leu352Val)	MYOM2 (L352V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467342	NM_003970.4(MYOM2):c.1066C>T (p.Arg356Cys)	MYOM2 (R356C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570397	NM_003970.4(MYOM2):c.1067G>T (p.Arg356Leu)	MYOM2 (R356L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403071	NM_003970.4(MYOM2):c.1084G>A (p.Gly362Ser)	MYOM2 (G362S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367271	NM_003970.4(MYOM2):c.1094A>T (p.Asp365Val)	MYOM2 (D365V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403557	NM_003970.4(MYOM2):c.1102G>A (p.Ala368Thr)	MYOM2 (A368T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608285	NM_003970.4(MYOM2):c.1121A>G (p.Asp374Gly)	MYOM2 (D374G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320491	NM_003970.4(MYOM2):c.1138A>G (p.Thr380Ala)	MYOM2 (T380A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168272	NM_003970.4(MYOM2):c.1145C>T (p.Ala382Val)	MYOM2 (A382V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561634	NM_003970.4(MYOM2):c.1150G>A (p.Gly384Ser)	MYOM2 (G384S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598720	NM_003970.4(MYOM2):c.1169A>G (p.Gln390Arg)	MYOM2 (Q390R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246442	NM_003970.4(MYOM2):c.1179C>G (p.Asp393Glu)	MYOM2 (D393E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168287	NM_003970.4(MYOM2):c.1184A>G (p.Asn395Ser)	MYOM2 (N395S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396212	NM_003970.4(MYOM2):c.1195G>A (p.Val399Ile)	MYOM2 (V399I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168296	NM_003970.4(MYOM2):c.1201G>A (p.Val401Met)	MYOM2 (V401M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168300	NM_003970.4(MYOM2):c.1306C>T (p.Pro436Ser)	MYOM2 (P436S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168302	NM_003970.4(MYOM2):c.1307C>T (p.Pro436Leu)	MYOM2 (P436L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395287	NM_003970.4(MYOM2):c.1328C>T (p.Pro443Leu)	MYOM2 (P443L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168309	NM_003970.4(MYOM2):c.1348G>A (p.Gly450Arg)	MYOM2 (G450R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168315	NM_003970.4(MYOM2):c.1403C>T (p.Pro468Leu)	MYOM2 (P468L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168322	NM_003970.4(MYOM2):c.1409G>A (p.Arg470Lys)	MYOM2 (R470K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369513	NM_003970.4(MYOM2):c.1426G>A (p.Ala476Thr)	MYOM2 (A476T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460968	NM_003970.4(MYOM2):c.1480G>C (p.Glu494Gln)	MYOM2 (E494Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362628	NM_003970.4(MYOM2):c.1480G>A (p.Glu494Lys)	MYOM2 (E494K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168342	NM_003970.4(MYOM2):c.1501C>G (p.Gln501Glu)	MYOM2 (Q501E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297398	NM_003970.4(MYOM2):c.1513G>A (p.Glu505Lys)	MYOM2 (E505K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266395	NM_003970.4(MYOM2):c.1532C>T (p.Pro511Leu)	MYOM2 (P511L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211764	NM_003970.4(MYOM2):c.1534G>A (p.Gly512Arg)	MYOM2 (G512R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236550	NM_003970.4(MYOM2):c.1537C>T (p.Pro513Ser)	MYOM2 (P513S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459086	NM_003970.4(MYOM2):c.1543A>G (p.Thr515Ala)	MYOM2 (T515A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168358	NM_003970.4(MYOM2):c.1609C>T (p.Arg537Cys)	MYOM2 (R537C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538986	NM_003970.4(MYOM2):c.1630T>G (p.Tyr544Asp)	MYOM2 (Y544D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168364	NM_003970.4(MYOM2):c.1637T>C (p.Ile546Thr)	MYOM2 (I546T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168366	NM_003970.4(MYOM2):c.1741T>G (p.Tyr581Asp)	MYOM2 (Y581D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509841	NM_003970.4(MYOM2):c.1769G>A (p.Arg590Gln)	MYOM2 (R590Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380934	NM_003970.4(MYOM2):c.1786C>T (p.Pro596Ser)	MYOM2 (P596S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207548	NM_003970.4(MYOM2):c.1849C>T (p.Arg617Trp)	MYOM2 (R617W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300327	NM_003970.4(MYOM2):c.1894T>G (p.Trp632Gly)	MYOM2 (W632G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518172	NM_003970.4(MYOM2):c.1899C>G (p.Asp633Glu)	MYOM2 (D633E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168378	NM_003970.4(MYOM2):c.1931A>G (p.Tyr644Cys)	MYOM2 (Y644C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168382	NM_003970.4(MYOM2):c.1946G>T (p.Cys649Phe)	MYOM2 (C649F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168385	NM_003970.4(MYOM2):c.1957A>G (p.Thr653Ala)	MYOM2 (T653A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336534	NM_003970.4(MYOM2):c.1983C>G (p.His661Gln)	MYOM2 (H661Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365766	NM_003970.4(MYOM2):c.2063A>G (p.Asn688Ser)	MYOM2 (N688S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168391	NM_003970.4(MYOM2):c.2076G>A (p.Met692Ile)	MYOM2 (M692I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483784	NM_003970.4(MYOM2):c.2090A>C (p.Gln697Pro)	MYOM2 (Q697P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168399	NM_003970.4(MYOM2):c.2155C>T (p.Leu719Phe)	MYOM2 (L719F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220411	NM_003970.4(MYOM2):c.2164T>C (p.Cys722Arg)	MYOM2 (C722R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606619	NM_003970.4(MYOM2):c.2179A>G (p.Met727Val)	MYOM2 (M727V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281622	NM_003970.4(MYOM2):c.2210G>T (p.Ser737Ile)	MYOM2 (S737I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454274	NM_003970.4(MYOM2):c.2219C>T (p.Ser740Leu)	MYOM2 (S740L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475727	NM_003970.4(MYOM2):c.2230G>A (p.Gly744Ser)	MYOM2 (G744S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525475	NM_003970.4(MYOM2):c.2231G>C (p.Gly744Ala)	MYOM2 (G744A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356180	NM_003970.4(MYOM2):c.2300C>T (p.Pro767Leu)	MYOM2 (P767L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375134	NM_003970.4(MYOM2):c.2305A>G (p.Ile769Val)	MYOM2 (I769V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309010	NM_003970.4(MYOM2):c.2353A>T (p.Ile785Phe)	MYOM2 (I785F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240594	NM_003970.4(MYOM2):c.2357C>A (p.Ala786Asp)	MYOM2 (A786D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368116	NM_003970.4(MYOM2):c.2374G>A (p.Gly792Ser)	MYOM2 (G792S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552003	NM_003970.4(MYOM2):c.2380G>T (p.Gly794Trp)	MYOM2 (G794W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212097	NM_003970.4(MYOM2):c.2380G>A (p.Gly794Arg)	MYOM2 (G794R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603250	NM_003970.4(MYOM2):c.2381G>A (p.Gly794Glu)	MYOM2 (G794E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215779	NM_003970.4(MYOM2):c.2399G>T (p.Ser800Ile)	MYOM2 (S800I)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2210638	NM_003970.4(MYOM2):c.2405A>G (p.His802Arg)	MYOM2 (H802R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596283	NM_003970.4(MYOM2):c.2408T>C (p.Phe803Ser)	MYOM2 (F803S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241157	NM_003970.4(MYOM2):c.2420C>T (p.Ala807Val)	MYOM2 (A807V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338004	NM_003970.4(MYOM2):c.2426C>G (p.Thr809Ser)	MYOM2 (T809S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3168468	NM_003970.4(MYOM2):c.2441G>C (p.Gly814Ala)	MYOM2 (G814A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207200	NM_003970.4(MYOM2):c.2459C>T (p.Thr820Met)	MYOM2 (T820M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336887	NM_003970.4(MYOM2):c.2504C>T (p.Ala835Val)	MYOM2 (A835V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363228	NM_003970.4(MYOM2):c.2582C>T (p.Thr861Ile)	MYOM2 (T861I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485595	NM_003970.4(MYOM2):c.2588A>G (p.Asn863Ser)	MYOM2 (N863S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589791	NM_003970.4(MYOM2):c.2594C>T (p.Thr865Met)	MYOM2 (T865M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533723	NM_003970.4(MYOM2):c.2596A>G (p.Thr866Ala)	MYOM2 (T866A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3168494	NM_003970.4(MYOM2):c.2679T>G (p.Asn893Lys)	LOC126264116, MYOM2 (N893K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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