"Ambry Genetics"[submitter] AND "MYH7B"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2541842	NM_020884.7(MYH7B):c.-119G>T	MYH7B	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2609602	NM_020884.7(MYH7B):c.-99G>T	MYH7B	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3297540	NM_020884.7(MYH7B):c.-46C>A	MYH7B	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2059297	NM_020884.7(MYH7B):c.-15C>T	MYH7B	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GUncertain significance
Select item 2484336	NM_020884.7(MYH7B):c.184A>G (p.Thr62Ala)	MYH7B (T62A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389014	NM_020884.7(MYH7B):c.196A>G (p.Lys66Glu)	MYH7B (K66E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 546896	NM_020884.7(MYH7B):c.266T>C (p.Met89Thr)	MYH7B (M89T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3158543	NM_020884.7(MYH7B):c.323A>T (p.Tyr108Phe)	MYH7B (Y108F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551119	NM_020884.7(MYH7B):c.355C>G (p.Leu119Val)	MYH7B (L119V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158609	NM_020884.7(MYH7B):c.409G>A (p.Val137Ile)	MYH7B (V137I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297534	NM_020884.7(MYH7B):c.416C>T (p.Ala139Val)	MYH7B (A139V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333238	NM_020884.7(MYH7B):c.470C>T (p.Ala157Val)	MYH7B (A157V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2200647	NM_020884.7(MYH7B):c.496C>T (p.Arg166Cys)	MYH7B (R166C)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2538151	NM_020884.7(MYH7B):c.511C>A (p.Gln171Lys)	MYH7B (Q171K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235070	NM_020884.7(MYH7B):c.514T>C (p.Ser172Pro)	MYH7B (S172P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158684	NM_020884.7(MYH7B):c.584C>T (p.Ala195Val)	MYH7B (A195V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299985	NM_020884.7(MYH7B):c.623C>T (p.Ala208Val)	MYH7B (A208V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2066952	NM_020884.7(MYH7B):c.644C>T (p.Thr215Met)	MYH7B (T215M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3297547	NM_020884.7(MYH7B):c.673G>A (p.Glu225Lys)	MYH7B (E225K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1478792	NM_020884.7(MYH7B):c.701G>C (p.Gly234Ala)	MYH7B (G234A)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1906766	NM_020884.7(MYH7B):c.755G>A (p.Arg252His)	MYH7B (R252H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3158699	NM_020884.7(MYH7B):c.757A>G (p.Ile253Val)	MYH7B (I253V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510818	NM_020884.7(MYH7B):c.823C>T (p.Arg275Trp)	MYH7B (R275W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1427692	NM_020884.7(MYH7B):c.842C>T (p.Pro281Leu)	MYH7B (P281L)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2470734	NM_020884.7(MYH7B):c.851G>A (p.Arg284His)	MYH7B (R284H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1450125	NM_020884.7(MYH7B):c.866A>G (p.Tyr289Cys)	MYH7B (Y289C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1505239	NM_020884.7(MYH7B):c.956G>C (p.Gly319Ala)	MYH7B (G319A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2291528	NM_020884.7(MYH7B):c.1036G>A (p.Val346Met)	MYH7B (V346M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1345638	NM_020884.7(MYH7B):c.1050T>G (p.Cys350Trp)	MYH7B (C350W)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2463832	NM_020884.7(MYH7B):c.1082A>G (p.His361Arg)	MYH7B (H361R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1385983	NM_020884.7(MYH7B):c.1093A>G (p.Met365Val)	MYH7B (M365V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2340588	NM_020884.7(MYH7B):c.1115G>A (p.Arg372Gln)	MYH7B (R372Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404188	NM_020884.7(MYH7B):c.1174G>C (p.Gly392Arg)	MYH7B (G392R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1475935	NM_020884.7(MYH7B):c.1210C>T (p.His404Tyr)	MYH7B (H404Y)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2520867	NM_020884.7(MYH7B):c.1223G>A (p.Arg408His)	MYH7B (R408H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1361399	NM_020884.7(MYH7B):c.1240G>A (p.Val414Met)	MYH7B (V414M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2523179	NM_020884.7(MYH7B):c.1248G>C (p.Lys416Asn)	MYH7B (K416N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2961155	NM_020884.7(MYH7B):c.1273T>G (p.Phe425Val)	MYH7B (F425V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2853813	NM_020884.7(MYH7B):c.1334G>A (p.Arg445Gln)	MYH7B (R445Q)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3297538	NM_020884.7(MYH7B):c.1381G>A (p.Gly461Arg)	MYH7B (G461R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494980	NM_020884.7(MYH7B):c.1400G>T (p.Gly467Val)	MYH7B (G467V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1485499	NM_020884.7(MYH7B):c.1516C>T (p.Arg506Trp)	MYH7B (R506W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1504009	NM_020884.7(MYH7B):c.1671C>A (p.Asp557Glu)	MYH7B (D557E)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2463784	NM_020884.7(MYH7B):c.1679C>T (p.Ala560Val)	MYH7B (A560V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3158447	NM_020884.7(MYH7B):c.1723C>T (p.Arg575Cys)	MYH7B (R575C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493271	NM_020884.7(MYH7B):c.1759G>A (p.Ala587Thr)	MYH7B (A587T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2061814	NM_020884.7(MYH7B):c.1820A>G (p.Glu607Gly)	MYH7B (E607G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2489279	NM_020884.7(MYH7B):c.1823C>T (p.Thr608Ile)	MYH7B (T608I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297537	NM_020884.7(MYH7B):c.1910C>G (p.Pro637Arg)	MYH7B (P637R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523434	NM_020884.7(MYH7B):c.2107A>G (p.Asn703Asp)	MYH7B (N703D)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3158459	NM_020884.7(MYH7B):c.2117T>G (p.Leu706Arg)	MYH7B (L706R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599383	NM_020884.7(MYH7B):c.2176C>T (p.Arg726Trp)	MYH7B (R726W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490084	NM_020884.7(MYH7B):c.2188C>T (p.Arg730Cys)	MYH7B (R730C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256277	NM_020884.7(MYH7B):c.2213C>T (p.Pro738Leu)	MYH7B (P738L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158472	NM_020884.7(MYH7B):c.2288A>T (p.Tyr763Phe)	MYH7B (Y763F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1297631	NM_020884.7(MYH7B):c.2393G>A (p.Arg798Gln)	MYH7B (R798Q)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2379771	NM_020884.7(MYH7B):c.2398C>T (p.Arg800Cys)	MYH7B (R800C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2412173	NM_020884.7(MYH7B):c.2413C>T (p.Arg805Cys)	MYH7B (R805C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1438525	NM_020884.7(MYH7B):c.2413C>G (p.Arg805Gly)	MYH7B (R805G)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2289932	NM_020884.7(MYH7B):c.2578C>T (p.Arg860Trp)	MYH7B (R860W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1426841	NM_020884.7(MYH7B):c.2582C>T (p.Ala861Val)	MYH7B (A861V)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1486620	NM_020884.7(MYH7B):c.2593G>A (p.Gly865Arg)	MYH7B (G865R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1360631	NM_020884.7(MYH7B):c.2600G>A (p.Arg867Gln)	MYH7B (R867Q)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1360293	NM_020884.7(MYH7B):c.2615C>T (p.Ala872Val)	MYH7B (A872V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3297541	NM_020884.7(MYH7B):c.2657G>A (p.Ser886Asn)	MYH7B (S886N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286686	NM_020884.7(MYH7B):c.2690A>G (p.Gln897Arg)	MYH7B (Q897R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211403	NM_020884.7(MYH7B):c.2706G>C (p.Gln902His)	MYH7B (Q902H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158502	NM_020884.7(MYH7B):c.2753C>T (p.Ser918Phe)	MYH7B (S918F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2137701	NM_020884.7(MYH7B):c.2864C>T (p.Thr955Met)	MYH7B (T955M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2206472	NM_020884.7(MYH7B):c.2980G>C (p.Glu994Gln)	MYH7B (E994Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1434074	NM_020884.7(MYH7B):c.3003G>T (p.Lys1001Asn)	MYH7B (K1001N)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1406684	NM_020884.7(MYH7B):c.3043G>A (p.Gly1015Ser)	MYH7B (G1015S)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2456761	NM_020884.7(MYH7B):c.3077C>T (p.Ala1026Val)	MYH7B (A1026V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3158514	NM_020884.7(MYH7B):c.3085A>G (p.Lys1029Glu)	MYH7B (K1029E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297530	NM_020884.7(MYH7B):c.3104A>G (p.Glu1035Gly)	MYH7B (E1035G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402113	NM_020884.7(MYH7B):c.3105G>T (p.Glu1035Asp)	MYH7B (E1035D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1397451	NM_020884.7(MYH7B):c.3146A>G (p.Lys1049Arg)	MYH7B (K1049R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2077786	NM_020884.7(MYH7B):c.3154C>T (p.Arg1052Cys)	MYH7B (R1052C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1509316	NM_020884.7(MYH7B):c.3226G>A (p.Ala1076Thr)	MYH7B (A1076T)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1484662	NM_020884.7(MYH7B):c.3241C>G (p.Gln1081Glu)	MYH7B (Q1081E)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3158518	NM_020884.7(MYH7B):c.3270G>C (p.Lys1090Asn)	MYH7B (K1090N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1482570	NM_020884.7(MYH7B):c.3299G>A (p.Arg1100Gln)	MYH7B (R1100Q)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3158520	NM_020884.7(MYH7B):c.3334C>G (p.Gln1112Glu)	MYH7B (Q1112E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468726	NM_020884.7(MYH7B):c.3336G>C (p.Gln1112His)	MYH7B (Q1112H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158522	NM_020884.7(MYH7B):c.3341A>T (p.Lys1114Met)	MYH7B (K1114M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158524	NM_020884.7(MYH7B):c.3413G>A (p.Arg1138His)	MYH7B (R1138H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1448829	NM_020884.7(MYH7B):c.3437C>T (p.Ala1146Val)	MYH7B (A1146V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2172166	NM_020884.7(MYH7B):c.3442C>T (p.Arg1148Trp)	MYH7B (R1148W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2075505	NM_020884.7(MYH7B):c.3454G>C (p.Glu1152Gln)	MYH7B (E1152Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2420153	NM_020884.7(MYH7B):c.3466C>T (p.Arg1156Trp)	MYH7B (R1156W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2338392	NM_020884.7(MYH7B):c.3484G>A (p.Gly1162Ser)	MYH7B (G1162S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297529	NM_020884.7(MYH7B):c.3515G>A (p.Arg1172His)	MYH7B (R1172H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293800	NM_020884.7(MYH7B):c.3520C>T (p.Arg1174Trp)	MYH7B (R1174W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341704	NM_020884.7(MYH7B):c.3540G>T (p.Arg1180Ser)	MYH7B (R1180S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297544	NM_020884.7(MYH7B):c.3544C>T (p.Arg1182Trp)	MYH7B (R1182W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158533	NM_020884.7(MYH7B):c.3602G>A (p.Arg1201His)	MYH7B (R1201H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2158593	NM_020884.7(MYH7B):c.3655C>T (p.Arg1219Trp)	MYH7B (R1219W)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1419796	NM_020884.7(MYH7B):c.3656G>A (p.Arg1219Gln)	MYH7B (R1219Q)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3158536	NM_020884.7(MYH7B):c.3662G>A (p.Arg1221Gln)	MYH7B (R1221Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594672	NM_020884.7(MYH7B):c.3698T>A (p.Met1233Lys)	MYH7B (M1233K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

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