ClinVar for Gene (Select 57644) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 3158684	NM_020884.7(MYH7B):c.584C>T (p.Ala195Val)	MYH7B (A195V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158640	NM_020884.7(MYH7B):c.5613G>A (p.Met1871Ile)	MYH7B (M1871I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158635	NM_020884.7(MYH7B):c.5590G>A (p.Asp1864Asn)	MYH7B (D1864N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158615	NM_020884.7(MYH7B):c.5267G>A (p.Arg1756Gln)	MYH7B (R1756Q)	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 3158600	NM_020884.7(MYH7B):c.5110C>T (p.Arg1704Cys)	MYH7B (R1704C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158588	NM_020884.7(MYH7B):c.4952G>T (p.Arg1651Leu)	MYH7B (R1651L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158579	NM_020884.7(MYH7B):c.4891G>A (p.Asp1631Asn)	MYH7B (D1631N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158578	NM_020884.7(MYH7B):c.4873A>G (p.Met1625Val)	MYH7B (M1625V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158576	NM_020884.7(MYH7B):c.4729G>C (p.Ala1577Pro)	MYH7B (A1577P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158560	NM_020884.7(MYH7B):c.4475G>A (p.Arg1492Gln)	MYH7B (R1492Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3158548	NM_020884.7(MYH7B):c.4391G>A (p.Arg1464Gln)	MYH7B (R1464Q)	Single nucleotide variant (missense variant)	not specified	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 3158541	NM_020884.7(MYH7B):c.3970C>T (p.Arg1324Cys)	MYH7B (R1324C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158540	NM_020884.7(MYH7B):c.3883A>G (p.Ser1295Gly)	MYH7B (S1295G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158538	NM_020884.7(MYH7B):c.3833C>T (p.Ala1278Val)	MYH7B (A1278V)	Single nucleotide variant (missense variant)	not specified	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 3158533	NM_020884.7(MYH7B):c.3602G>A (p.Arg1201His)	MYH7B (R1201H)	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 3158522	NM_020884.7(MYH7B):c.3341A>T (p.Lys1114Met)	MYH7B (K1114M)	Single nucleotide variant (missense variant)	not specified	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 3158518	NM_020884.7(MYH7B):c.3270G>C (p.Lys1090Asn)	MYH7B (K1090N)	Single nucleotide variant (missense variant)	not specified	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 3158502	NM_020884.7(MYH7B):c.2753C>T (p.Ser918Phe)	MYH7B (S918F)	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 3158459	NM_020884.7(MYH7B):c.2117T>G (p.Leu706Arg)	MYH7B (L706R)	Single nucleotide variant (missense variant)	not specified	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 3055329	NM_020884.7(MYH7B):c.4617G>A (p.Ala1539=)	MYH7B	Single nucleotide variant (synonymous variant)	MYH7B-related disorder	GLikely benign
Select item 3047739	NM_020884.7(MYH7B):c.4854G>A (p.Ala1618=)	MYH7B	Single nucleotide variant (synonymous variant)	MYH7B-related disorder	GLikely benign
Select item 3042866	NM_020884.7(MYH7B):c.5581-7C>T	MYH7B	Single nucleotide variant (intron variant)	MYH7B-related disorder	GLikely benign
Select item 3041489	NM_020884.7(MYH7B):c.2183+10C>T	MYH7B	Single nucleotide variant (intron variant)	MYH7B-related disorder	GLikely benign
Select item 3039456	NM_020884.7(MYH7B):c.1761A>G (p.Ala587=)	MYH7B	Single nucleotide variant (synonymous variant)	MYH7B-related disorder	GLikely benign
Select item 3039259	NM_020884.7(MYH7B):c.1758C>T (p.Tyr586=)	MYH7B	Single nucleotide variant (synonymous variant)	MYH7B-related disorder	GLikely benign
Select item 3034560	NM_020884.7(MYH7B):c.5319C>T (p.Ala1773=)	MYH7B	Single nucleotide variant (synonymous variant)	MYH7B-related disorder	GLikely benign
Select item 3023280	NM_020884.7(MYH7B):c.2444+18G>C	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3022386	NM_020884.7(MYH7B):c.216A>G (p.Glu72=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3022263	NM_020884.7(MYH7B):c.5677-13T>C	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3021694	NM_020884.7(MYH7B):c.2813A>T (p.Glu938Val)	MYH7B (E938V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3021204	NM_020884.7(MYH7B):c.905-6C>T	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3021049	NM_020884.7(MYH7B):c.132C>T (p.Tyr44=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3017272	NM_020884.7(MYH7B):c.2183+1G>A	MYH7B	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 3015604	NM_020884.7(MYH7B):c.2504C>T (p.Ser835Leu)	MYH7B (S835L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3014977	NM_020884.7(MYH7B):c.2606C>T (p.Ala869Val)	MYH7B (A869V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3013965	NM_020884.7(MYH7B):c.2543G>A (p.Arg848His)	MYH7B (R848H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3012900	NM_020884.7(MYH7B):c.2265G>C (p.Ser755=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3012386	NM_020884.7(MYH7B):c.2973G>A (p.Ala991=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3009886	NM_020884.7(MYH7B):c.3207G>A (p.Thr1069=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3007815	NM_020884.7(MYH7B):c.4947C>T (p.Ala1649=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3007377	NM_020884.7(MYH7B):c.4191-4C>T	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005921	NM_020884.7(MYH7B):c.4372C>T (p.Arg1458Trp)	MYH7B (R1458W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3003494	NM_020884.7(MYH7B):c.5012C>G (p.Ala1671Gly)	MYH7B (A1671G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3002513	NM_020884.7(MYH7B):c.5095C>T (p.Leu1699=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3000896	NM_020884.7(MYH7B):c.343-15A>G	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2995819	NM_020884.7(MYH7B):c.620A>G (p.Lys207Arg)	MYH7B (K207R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2994800	NM_020884.7(MYH7B):c.4570A>T (p.Ser1524Cys)	MYH7B (S1524C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2993249	NM_020884.7(MYH7B):c.833_834insA (p.Phe278fs)	MYH7B (F278fs)	Insertion (frameshift variant)	not provided	GUncertain significance
Select item 2992038	NM_020884.7(MYH7B):c.4795C>T (p.Arg1599Ter)	MYH7B (R1599*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2991101	NM_020884.7(MYH7B):c.3253G>A (p.Glu1085Lys)	MYH7B (E1085K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2991075	NM_020884.7(MYH7B):c.91+15_91+16del	MYH7B	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2990493	NM_020884.7(MYH7B):c.1152T>C (p.Ala384=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2986997	NM_020884.7(MYH7B):c.1266+6C>T	MYH7B	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2985555	NM_020884.7(MYH7B):c.527+11G>A	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2985325	NM_020884.7(MYH7B):c.435C>T (p.Arg145=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2983876	NM_020884.7(MYH7B):c.592G>A (p.Ala198Thr)	MYH7B (A198T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2980218	NM_020884.7(MYH7B):c.3277G>A (p.Glu1093Lys)	MYH7B (E1093K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2979202	NM_020884.7(MYH7B):c.625-17C>T	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2978563	NM_020884.7(MYH7B):c.3483C>T (p.Gly1161=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2978173	NM_020884.7(MYH7B):c.2392C>T (p.Arg798Trp)	MYH7B (R798W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2976857	NM_020884.7(MYH7B):c.342+15C>G	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2975997	NM_020884.7(MYH7B):c.3357+13C>T	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2975397	NM_020884.7(MYH7B):c.2039T>C (p.Ile680Thr)	MYH7B (I680T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2975330	NM_020884.7(MYH7B):c.2146T>C (p.Phe716Leu)	MYH7B (F716L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2972316	NM_020884.7(MYH7B):c.1008+1G>A	MYH7B	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 2972196	NM_020884.7(MYH7B):c.3309C>T (p.Asp1103=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2971231	NM_020884.7(MYH7B):c.121C>G (p.Gln41Glu)	MYH7B (Q41E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2970459	NM_020884.7(MYH7B):c.3390G>A (p.Glu1130=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2969951	NM_020884.7(MYH7B):c.3695G>A (p.Arg1232His)	MYH7B (R1232H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2968256	NM_020884.7(MYH7B):c.4540+4G>A	MYH7B	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2967566	NM_020884.7(MYH7B):c.4782-19T>C	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2967549	NM_020884.7(MYH7B):c.2701-14C>T	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2967480	NM_020884.7(MYH7B):c.5064G>A (p.Leu1688=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2966780	NM_020884.7(MYH7B):c.87G>A (p.Trp29Ter)	MYH7B (W29*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2965664	NM_020884.7(MYH7B):c.5306C>A (p.Ala1769Glu)	MYH7B (A1769E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2965228	NM_020884.7(MYH7B):c.-71G>A	MYH7B	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 2964760	NM_020884.7(MYH7B):c.2183+17C>A	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2962775	NM_020884.7(MYH7B):c.-73+14G>A	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961730	NM_020884.7(MYH7B):c.2183+12C>T	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961224	NM_020884.7(MYH7B):c.5156G>A (p.Arg1719His)	MYH7B (R1719H)	Single nucleotide variant (missense variant)	not provided	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 2960835	NM_020884.7(MYH7B):c.5305-1G>T	MYH7B	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 2958511	NM_020884.7(MYH7B):c.606C>T (p.Asp202=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957903	NM_020884.7(MYH7B):c.2228T>C (p.Met743Thr)	MYH7B (M743T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2957196	NM_020884.7(MYH7B):c.3993+14G>A	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2957148	NM_020884.7(MYH7B):c.3467G>C (p.Arg1156Pro)	MYH7B (R1156P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2956659	NM_020884.7(MYH7B):c.1900+14G>A	MYH7B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2956544	NM_020884.7(MYH7B):c.2882T>C (p.Ile961Thr)	MYH7B (I961T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2956495	NM_020884.7(MYH7B):c.5676+7G>A	MYH7B	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2956494	NM_020884.7(MYH7B):c.3451G>A (p.Glu1151Lys)	MYH7B (E1151K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2956124	NM_020884.7(MYH7B):c.3276C>T (p.Ser1092=)	MYH7B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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