"Ambry Genetics"[submitter] AND "MYH10"[gene] - ClinVar

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Items: 74

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2220187	NM_001256012.3(MYH10):c.5978G>C (p.Ser1993Thr)	MYH10 (S1972T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2397412	NM_001256012.3(MYH10):c.5930T>C (p.Leu1977Pro)	MYH10 (L1946P +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3156108	NM_001256012.3(MYH10):c.5920C>T (p.Arg1974Trp)	MYH10 (R1952W +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2532112	NM_001256012.3(MYH10):c.5912G>C (p.Arg1971Pro)	MYH10 (R1971P +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2444573	NM_001256012.3(MYH10):c.5881C>T (p.Arg1961Trp)	MYH10 (R1930W +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2517955	NM_001256012.3(MYH10):c.5849G>A (p.Arg1950His)	LOC125177414, MYH10 (R1919H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2551274	NM_001256012.3(MYH10):c.5836G>C (p.Glu1946Gln)	LOC125177414, MYH10 (E1924Q +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2333408	NM_001256012.3(MYH10):c.5806C>T (p.Arg1936Trp)	LOC125177414, MYH10 (R1914W +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3156090	NM_001256012.3(MYH10):c.5686G>A (p.Ala1896Thr)	MYH10 (A1874T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471802	NM_001256012.3(MYH10):c.5630G>A (p.Arg1877His)	MYH10 (R1846H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2208911	NM_001256012.3(MYH10):c.5608G>A (p.Ala1870Thr)	MYH10 (A1848T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2219799	NM_001256012.3(MYH10):c.5582T>G (p.Leu1861Arg)	MYH10 (L1830R +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2255637	NM_001256012.3(MYH10):c.5531A>T (p.Lys1844Met)	MYH10 (K1813M +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2409411	NM_001256012.3(MYH10):c.5453G>A (p.Arg1818His)	MYH10 (R1818H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2336270	NM_001256012.3(MYH10):c.5389G>A (p.Val1797Met)	MYH10 (V1766M +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3156064	NM_001256012.3(MYH10):c.5370C>A (p.Phe1790Leu)	MYH10 (F1768L +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3156061	NM_001256012.3(MYH10):c.5318A>G (p.Glu1773Gly)	MYH10 (E1751G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2461427	NM_001256012.3(MYH10):c.5303G>A (p.Arg1768Gln)	MYH10 (R1768Q +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2204931	NM_001256012.3(MYH10):c.5290C>T (p.Arg1764Cys)	MYH10 (R1764C +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2591326	NM_001256012.3(MYH10):c.5288G>T (p.Arg1763Leu)	MYH10 (R1741L +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3156048	NM_001256012.3(MYH10):c.5269G>A (p.Ala1757Thr)	MYH10 (A1757T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3156044	NM_001256012.3(MYH10):c.5215C>G (p.Gln1739Glu)	MYH10 (Q1739E +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378655	NM_001256012.3(MYH10):c.5087G>A (p.Arg1696His)	MYH10 (R1665H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2465211	NM_001256012.3(MYH10):c.5069G>A (p.Arg1690His)	MYH10 (R1659H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2391727	NM_001256012.3(MYH10):c.4981G>A (p.Glu1661Lys)	MYH10 (E1630K +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2603641	NM_001256012.3(MYH10):c.4889G>A (p.Arg1630Gln)	MYH10 (R1599Q +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2266069	NM_001256012.3(MYH10):c.4838C>T (p.Thr1613Ile)	MYH10 (T1591I +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3297344	NM_001256012.3(MYH10):c.4821C>G (p.Phe1607Leu)	MYH10 (F1586L +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3297342	NM_001256012.3(MYH10):c.4808T>G (p.Met1603Arg)	MYH10 (M1581R +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3297339	NM_001256012.3(MYH10):c.4696C>T (p.Arg1566Trp)	MYH10 (R1544W +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2404500	NM_001256012.3(MYH10):c.4511G>A (p.Arg1504Gln)	MYH10 (R1483Q +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2347736	NM_001256012.3(MYH10):c.4510C>T (p.Arg1504Trp)	MYH10 (R1483W +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3297343	NM_001256012.3(MYH10):c.4417G>A (p.Val1473Ile)	MYH10 (V1442I +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2387935	NM_001256012.3(MYH10):c.4313G>A (p.Arg1438His)	MYH10 (R1407H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3297341	NM_001256012.3(MYH10):c.4279A>C (p.Lys1427Gln)	MYH10 (K1396Q +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3156017	NM_001256012.3(MYH10):c.4252A>G (p.Ile1418Val)	MYH10 (I1387V +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3156009	NM_001256012.3(MYH10):c.4240G>A (p.Asp1414Asn)	MYH10 (D1383N +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2325656	NM_001256012.3(MYH10):c.4240G>T (p.Asp1414Tyr)	MYH10 (D1383Y +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3156006	NM_001256012.3(MYH10):c.4107C>G (p.Ile1369Met)	MYH10 (I1348M +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2256023	NM_001256012.3(MYH10):c.4105A>G (p.Ile1369Val)	MYH10 (I1348V +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2286184	NM_001256012.3(MYH10):c.4001G>T (p.Gly1334Val)	MYH10 (G1312V +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2236800	NM_001256012.3(MYH10):c.3994A>G (p.Lys1332Glu)	MYH10 (K1301E +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155994	NM_001256012.3(MYH10):c.3868G>A (p.Ala1290Thr)	MYH10 (A1259T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2602116	NM_001256012.3(MYH10):c.3803C>T (p.Ala1268Val)	MYH10 (A1246V +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2525982	NM_001256012.3(MYH10):c.3776G>T (p.Gly1259Val)	MYH10 (G1237V +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3297337	NM_001256012.3(MYH10):c.3697G>A (p.Ala1233Thr)	MYH10 (A1202T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2247198	NM_001256012.3(MYH10):c.3465G>T (p.Gln1155His)	MYH10 (Q1124H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2532483	NM_001256012.3(MYH10):c.3445G>T (p.Ala1149Ser)	MYH10 (A1118S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155991	NM_001256012.3(MYH10):c.3365A>C (p.Glu1122Ala)	MYH10 (E1091A +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2536218	NM_001256012.3(MYH10):c.3326T>C (p.Ile1109Thr)	MYH10 (I1078T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155988	NM_001256012.3(MYH10):c.3319G>T (p.Ala1107Ser)	MYH10 (A1086S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2222395	NM_001256012.3(MYH10):c.3307G>A (p.Ala1103Thr)	MYH10 (A1072T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 618227	NM_001256012.3(MYH10):c.3276C>A (p.Asp1092Glu)	MYH10 (D1092E +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2558615	NM_001256012.3(MYH10):c.3238A>G (p.Thr1080Ala)	MYH10 (T1080A +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2275784	NM_001256012.3(MYH10):c.3158C>T (p.Ala1053Val)	MYH10 (A1053V +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3297340	NM_001256012.3(MYH10):c.3112C>G (p.Arg1038Gly)	MYH10 (R1017G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2621897	NM_001256012.3(MYH10):c.3052A>T (p.Ile1018Phe)	MYH10 (I987F +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 208680	NM_001256012.3(MYH10):c.2815G>T (p.Glu939Ter)	MYH10 (E908* +3 more)	Single nucleotide variant (nonsense)	Inborn genetic diseases	GPathogenic
Select item 3155985	NM_001256012.3(MYH10):c.2699C>T (p.Thr900Met)	LOC126862486, MYH10 (T878M +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155984	NM_001256012.3(MYH10):c.2687A>G (p.Lys896Arg)	LOC126862486, MYH10 (K865R +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155981	NM_001256012.3(MYH10):c.2120T>C (p.Val707Ala)	MYH10 (V686A +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3297346	NM_001256012.3(MYH10):c.2099G>A (p.Arg700Gln)	MYH10 (R669Q +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2245914	NM_001256012.3(MYH10):c.2051T>G (p.Val684Gly)	MYH10 (V653G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155980	NM_001256012.3(MYH10):c.1835A>G (p.Asn612Ser)	MYH10 (N612S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2217495	NM_001256012.3(MYH10):c.1821C>G (p.Asp607Glu)	MYH10 (D597E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2227380	NM_001256012.3(MYH10):c.1564G>A (p.Gly522Arg)	MYH10 (G521R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3297338	NM_001256012.3(MYH10):c.1544A>G (p.Glu515Gly)	MYH10 (E505G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3155967	NM_001256012.3(MYH10):c.1394T>C (p.Ile465Thr)	MYH10 (I464T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2327858	NM_001256012.3(MYH10):c.1316A>G (p.Tyr439Cys)	MYH10 (Y439C +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3156115	NM_001256012.3(MYH10):c.979A>G (p.Ile327Val)	MYH10 (I327V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2465250	NM_001256012.3(MYH10):c.677G>A (p.Arg226Gln)	MYH10 (R216Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3156025	NM_001256012.3(MYH10):c.467C>G (p.Ala156Gly)	MYH10 (A156G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2239320	NM_001256012.3(MYH10):c.161G>A (p.Arg54Gln)	MYH10 (R54Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2255638	NM_001256012.3(MYH10):c.56C>T (p.Ala19Val)	MYH10 (A19V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 74