"GeneDx"[submitter] AND "MYH10"[gene] - ClinVar

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Items: 57

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1712638	NM_001256012.3(MYH10):c.5907del (p.Ser1970fs)	MYH10 (S1939fs +3 more)	Deletion (frameshift variant)	not provided	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 2576873	NM_001256012.3(MYH10):c.5858G>C (p.Ser1953Thr)	LOC125177414, MYH10 (S1922T +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2662056	NM_001256012.3(MYH10):c.5696dup (p.Tyr1899Ter)	MYH10 (Y1868* +3 more)	Duplication (nonsense)	not provided	GUncertain significance
Select item 2662319	NM_001256012.3(MYH10):c.5581C>T (p.Leu1861Phe)	MYH10 (L1830F +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2446594	NM_001256012.3(MYH10):c.5458dup (p.Gln1820fs)	MYH10 (Q1789fs +3 more)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 1710856	NM_001256012.3(MYH10):c.5448T>A (p.Asn1816Lys)	MYH10 (N1785K +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2443437	NM_001256012.3(MYH10):c.5426G>T (p.Ser1809Ile)	MYH10 (S1778I +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3370992	NM_001256012.3(MYH10):c.5348T>C (p.Met1783Thr)	MYH10 (M1752T +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3363215	NM_001256012.3(MYH10):c.5245A>C (p.Thr1749Pro)	MYH10 (T1718P +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1181228	NM_001256012.3(MYH10):c.5175+17_5175+18insATTC	MYH10	Insertion (intron variant)	not provided	GBenign
Select item 1256834	NM_001256012.3(MYH10):c.5046+18T>C	MYH10	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281424	NM_001256012.3(MYH10):c.4885-1241C>T	MYH10	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3371125	NM_001256012.3(MYH10):c.4649C>T (p.Ser1550Phe)	MYH10 (S1519F +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3253015	NM_001256012.3(MYH10):c.4621C>T (p.Arg1541Ter)	MYH10 (R1510* +3 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 3371119	NM_001256012.3(MYH10):c.4544A>G (p.Lys1515Arg)	MYH10 (K1484R +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2662113	NM_001256012.3(MYH10):c.4492T>C (p.Tyr1498His)	MYH10 (Y1467H +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2444609	NM_001256012.3(MYH10):c.4150G>C (p.Glu1384Gln)	MYH10 (E1353Q +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367318	NM_001256012.3(MYH10):c.4113G>C (p.Gln1371His)	MYH10 (Q1340H +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3369512	NM_001256012.3(MYH10):c.4060C>G (p.Leu1354Val)	MYH10 (L1323V +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3252544	NM_001256012.3(MYH10):c.4057-6A>G	MYH10	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1804481	NM_001256012.3(MYH10):c.4017G>C (p.Lys1339Asn)	MYH10 (K1308N +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3253432	NM_001256012.3(MYH10):c.3997A>G (p.Lys1333Glu)	MYH10 (K1302E +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2501890	NM_001256012.3(MYH10):c.3937G>A (p.Ala1313Thr)	MYH10 (A1282T +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368606	NM_001256012.3(MYH10):c.3632A>C (p.Lys1211Thr)	MYH10 (K1180T +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2428853	NM_001256012.3(MYH10):c.3599+2T>G	MYH10	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 3372160	NM_001256012.3(MYH10):c.3303G>C (p.Gln1101His)	MYH10 (Q1070H +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3369631	NM_001256012.3(MYH10):c.3239C>T (p.Thr1080Ile)	MYH10 (T1049I +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3372889	NM_001256012.3(MYH10):c.3013del (p.Lys1004_Val1005insTer)	MYH10	Deletion (nonsense)	not provided	GUncertain significance
Select item 3378127	NM_001256012.3(MYH10):c.2821A>T (p.Arg941Trp)	MYH10 (R910W +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1326602	NM_001256012.3(MYH10):c.2700G>A (p.Thr900=)	LOC126862486, MYH10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2573803	NM_001256012.3(MYH10):c.2591A>G (p.Gln864Arg)	LOC126862486, MYH10 (Q833R +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2446599	NM_001256012.3(MYH10):c.2276A>G (p.Tyr759Cys)	MYH10 (Y728C +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2502628	NM_001256012.3(MYH10):c.2265C>G (p.Phe755Leu)	MYH10 (F724L +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2580613	NM_001256012.3(MYH10):c.2227C>T (p.Arg743Cys)	MYH10 (R712C +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367616	NM_001256012.3(MYH10):c.2186A>G (p.Gln729Arg)	MYH10 (Q698R +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2499832	NM_001256012.3(MYH10):c.2164G>T (p.Asp722Tyr)	MYH10 (D691Y +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1703439	NM_001256012.3(MYH10):c.2036G>A (p.Gly679Asp)	MYH10 (G648D +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2444807	NM_001256012.3(MYH10):c.1895A>C (p.Glu632Ala)	MYH10 (E632A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2577680	NM_001256012.3(MYH10):c.1838T>C (p.Val613Ala)	MYH10 (V603A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2505937	NM_001256012.3(MYH10):c.1759A>G (p.Ile587Val)	MYH10 (I577V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1801922	NM_001256012.3(MYH10):c.1363G>T (p.Asp455Tyr)	MYH10 (D445Y +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2571836	NM_001256012.3(MYH10):c.1282G>C (p.Asp428His)	MYH10 (D418H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3370807	NM_001256012.3(MYH10):c.1259A>G (p.Lys420Arg)	MYH10 (K410R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3253330	NM_001256012.3(MYH10):c.1183C>A (p.Leu395Ile)	MYH10 (L385I +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2580810	NM_001256012.3(MYH10):c.635A>T (p.Gln212Leu)	MYH10 (Q212L)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2501439	NM_001256012.3(MYH10):c.584T>C (p.Leu195Pro)	MYH10 (L195P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3364448	NM_001256012.3(MYH10):c.574A>G (p.Ile192Val)	MYH10 (I192V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2430644	NM_001256012.3(MYH10):c.566A>G (p.Lys189Arg)	MYH10 (K189R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2663037	NM_001256012.3(MYH10):c.531-2A>C	MYH10	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 2662918	NM_001256012.3(MYH10):c.350A>G (p.Tyr117Cys)	MYH10 (Y117C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361590	NM_001256012.3(MYH10):c.3976C>T (p.Leu1326Phe)	MYH10 (L1295F +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361584	NM_001256012.3(MYH10):c.1678G>C (p.Val560Leu)	MYH10 (V550L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361275	NM_001256012.3(MYH10):c.3043G>C (p.Glu1015Gln)	MYH10 (E1015Q +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3359740	NM_001256012.3(MYH10):c.4477A>T (p.Ser1493Cys)	MYH10 (S1462C +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3359665	NM_001256012.3(MYH10):c.3200T>G (p.Ile1067Ser)	MYH10 (I1036S +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3359508	NM_001256012.3(MYH10):c.1716G>C (p.Lys572Asn)	MYH10 (K562N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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Items: 57