| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23423546C>A | CA389045615 | MYH7 | c.3099+1G>T (n.3099+1G>T) n.3205+1G>T | |
| 14 | g.23423546C= | CA2123452970 | MYH7 | c.3099+1G= (n.3099+1G=) n.3205+1G= | |
| 14 | g.23423546C>G | CA257818688 | MYH7 | c.3099+1G>C (n.3099+1G>C) n.3205+1G>C | dbSNP |
| 14 | g.23423546C>T | CA389045616 | MYH7 | c.3099+1G>A (n.3099+1G>A) n.3205+1G>A | |
| 14 | g.23423547A= | CA2123452980 | MYH7 | c.3099T= (p.Asp1033=) n.3205T= | |
| 14 | g.23423547A>C | CA389045618 | MYH7 | c.3099T>G (p.Asp1033Glu) n.3205T>G | |
| 14 | g.23423547A>G | CA035538 | MYH7 | c.3099T>C (p.Asp1033=) n.3205T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23423547A>T | CA16614485 | MYH7 | c.3099T>A (p.Asp1033Glu) n.3205T>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23423548T>A | CA389045621 | MYH7 | c.3098A>T (p.Asp1033Val) n.3204A>T | dbSNP |
| 14 | g.23423548T>C | CA389045622 | MYH7 | c.3098A>G (p.Asp1033Gly) n.3204A>G | COSMIC |
| 14 | g.23423548T>G | CA389045623 | MYH7 | c.3098A>C (p.Asp1033Ala) n.3204A>C | |
| 14 | g.23423548T= | CA2123452986 | MYH7 | c.3098A= (p.Asp1033=) n.3204A= | |
| 14 | g.23423549C>A | CA389045625 | MYH7 | c.3097G>T (p.Asp1033Tyr) n.3203G>T | |
| 14 | g.23423549C>G | CA389045627 | MYH7 | c.3097G>C (p.Asp1033His) n.3203G>C | |
| 14 | g.23423549C>T | CA389045628 | MYH7 | c.3097G>A (p.Asp1033Asn) n.3203G>A | |
| 14 | g.23423550A>C | CA389045630 | MYH7 | c.3096T>G (p.Asp1032Glu) n.3202T>G | |
| 14 | g.23423550A>G | CA485622523 | MYH7 | c.3096T>C (p.Asp1032=) n.3202T>C | |
| 14 | g.23423550A>T | CA389045631 | MYH7 | c.3096T>A (p.Asp1032Glu) n.3202T>A | |
| 14 | g.23423551T>A | CA389045632 | MYH7 | c.3095A>T (p.Asp1032Val) n.3201A>T | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23423551T>C | CA389045634 | MYH7 | c.3095A>G (p.Asp1032Gly) n.3201A>G | |
| 14 | g.23423551T>G | CA389045636 | MYH7 | c.3095A>C (p.Asp1032Ala) n.3201A>C | |
| 14 | g.23423551T= | CA2123452989 | MYH7 | c.3095A= (p.Asp1032=) n.3201A= | |
| 14 | g.23423552C>A | CA389045638 | MYH7 | c.3094G>T (p.Asp1032Tyr) n.3200G>T | |
| 14 | g.23423552C= | CA2123452994 | MYH7 | c.3094G= (p.Asp1032=) n.3200G= | |
| 14 | g.23423552C>G | CA389045639 | MYH7 | c.3094G>C (p.Asp1032His) n.3200G>C | gnomAD v4 |
| 14 | g.23423552C>T | CA013351 | MYH7 | c.3094G>A (p.Asp1032Asn) n.3200G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423553del | CA2624235974 | MYH7 | c.3094del (p.Asp1032MetfsTer28) n.3200del | ClinVar gnomAD v4 |
| 14 | g.23423553C>A | CA485622525 | MYH7 | c.3093G>T (p.Val1031=) n.3199G>T | |
| 14 | g.23423553C>G | CA485622526 | MYH7 | c.3093G>C (p.Val1031=) n.3199G>C | ClinVar gnomAD v4 |
| 14 | g.23423553C>T | CA485622527 | MYH7 | c.3093G>A (p.Val1031=) n.3199G>A | |
| 14 | g.23423554A= | CA2123452998 | MYH7 | c.3092T= (p.Val1031=) n.3198T= | |
| 14 | g.23423554A>C | CA389045645 | MYH7 | c.3092T>G (p.Val1031Gly) n.3198T>G | |
| 14 | g.23423554A>G | CA389045641 | MYH7 | c.3092T>C (p.Val1031Ala) n.3198T>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23423554A>T | CA389045643 | MYH7 | c.3092T>A (p.Val1031Glu) n.3198T>A | |
| 14 | g.23423555C>A | CA389045646 | MYH7 | c.3091G>T (p.Val1031Leu) n.3197G>T | |
| 14 | g.23423555C>G | CA389045647 | MYH7 | c.3091G>C (p.Val1031Leu) n.3197G>C | ClinVar |
| 14 | g.23423555C>T | CA389045648 | MYH7 | c.3091G>A (p.Val1031Met) n.3197G>A | |
| 14 | g.23423556T>A | CA389045650 | MYH7 | c.3090A>T (p.Gln1030His) n.3196A>T | |
| 14 | g.23423556T>C | CA485622532 | MYH7 | c.3090A>G (p.Gln1030=) n.3196A>G | |
| 14 | g.23423556T>G | CA257818692 | MYH7 | c.3090A>C (p.Gln1030His) n.3196A>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23423556T= | CA2123453005 | MYH7 | c.3090A= (p.Gln1030=) n.3196A= | |
| 14 | g.23423557T>A | CA389045653 | MYH7 | c.3089A>T (p.Gln1030Leu) n.3195A>T | |
| 14 | g.23423557T>C | CA035461 | MYH7 | c.3089A>G (p.Gln1030Arg) n.3195A>G | dbSNP ExAC gnomAD v2 |
| 14 | g.23423557T>G | CA389045654 | MYH7 | c.3089A>C (p.Gln1030Pro) n.3195A>C | |
| 14 | g.23423557T= | CA2123453016 | MYH7 | c.3089A= (p.Gln1030=) n.3195A= | |
| 14 | g.23423558G>A | CA389045655 | MYH7 | c.3088C>T (p.Gln1030Ter) n.3194C>T | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23423558G>C | CA389045657 | MYH7 | c.3088C>G (p.Gln1030Glu) n.3194C>G | |
| 14 | g.23423558G= | CA2123453020 | MYH7 | c.3088C= (p.Gln1030=) n.3194C= | |
| 14 | g.23423558G>T | CA389045658 | MYH7 | c.3088C>A (p.Gln1030Lys) n.3194C>A | |
| 14 | g.23423559C>A | CA389045660 | MYH7 | c.3087G>T (p.Gln1029His) n.3193G>T | |
| 14 | g.23423559C>G | CA389045661 | MYH7 | c.3087G>C (p.Gln1029His) n.3193G>C | |
| 14 | g.23423559C>T | CA485622534 | MYH7 | c.3087G>A (p.Gln1029=) n.3193G>A | |
| 14 | g.23423560T>A | CA389045662 | MYH7 | c.3086A>T (p.Gln1029Leu) n.3192A>T | |
| 14 | g.23423560T>C | CA389045663 | MYH7 | c.3086A>G (p.Gln1029Arg) n.3192A>G | |
| 14 | g.23423560T>G | CA389045664 | MYH7 | c.3086A>C (p.Gln1029Pro) n.3192A>C | ClinVar dbSNP |
| 14 | g.23423560T= | CA2123453025 | MYH7 | c.3086A= (p.Gln1029=) n.3192A= | |
| 14 | g.23423561G>A | CA389045666 | MYH7 | c.3085C>T (p.Gln1029Ter) n.3191C>T | |
| 14 | g.23423561G>C | CA389045667 | MYH7 | c.3085C>G (p.Gln1029Glu) n.3191C>G | ClinVar gnomAD v4 |
| 14 | g.23423561G>T | CA389045668 | MYH7 | c.3085C>A (p.Gln1029Lys) n.3191C>A | |
| 14 | g.23423562C>A | CA389045669 | MYH7 | c.3084G>T (p.Glu1028Asp) n.3190G>T | |
| 14 | g.23423562C>G | CA389045670 | MYH7 | c.3084G>C (p.Glu1028Asp) n.3190G>C | |
| 14 | g.23423562C>T | CA485622538 | MYH7 | c.3084G>A (p.Glu1028=) n.3190G>A | ClinVar dbSNP gnomAD v4 COSMIC |
| 14 | g.23423563T>A | CA389045671 | MYH7 | c.3083A>T (p.Glu1028Val) n.3189A>T | |
| 14 | g.23423563T>C | CA013343 | MYH7 | c.3083A>G (p.Glu1028Gly) n.3189A>G | ClinVar dbSNP gnomAD v4 |
| 14 | g.23423563T>G | CA389045673 | MYH7 | c.3083A>C (p.Glu1028Ala) n.3189A>C | |
| 14 | g.23423563T= | CA2123453031 | MYH7 | c.3083A= (p.Glu1028=) n.3189A= | |
| 14 | g.23423564C>A | CA389045674 | MYH7 | c.3082G>T (p.Glu1028Ter) n.3188G>T | |
| 14 | g.23423564C>G | CA389045676 | MYH7 | c.3082G>C (p.Glu1028Gln) n.3188G>C | gnomAD v4 COSMIC |
| 14 | g.23423564C>T | CA389045677 | MYH7 | c.3082G>A (p.Glu1028Lys) n.3188G>A | gnomAD v4 |
| 14 | g.23423565C>A | CA485622539 | MYH7 | c.3081G>T (p.Leu1027=) n.3187G>T | |
| 14 | g.23423565C>G | CA485622540 | MYH7 | c.3081G>C (p.Leu1027=) n.3187G>C | |
| 14 | g.23423565C>T | CA485622541 | MYH7 | c.3081G>A (p.Leu1027=) n.3187G>A | |
| 14 | g.23423566A>C | CA389045678 | MYH7 | c.3080T>G (p.Leu1027Arg) n.3186T>G | gnomAD v4 |
| 14 | g.23423566A>G | CA389045680 | MYH7 | c.3080T>C (p.Leu1027Pro) n.3186T>C | |
| 14 | g.23423566A>T | CA389045682 | MYH7 | c.3080T>A (p.Leu1027Gln) n.3186T>A | |
| 14 | g.23423567G>A | CA035450 | MYH7 | c.3079C>T (p.Leu1027=) n.3185C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23423567G>C | CA389045684 | MYH7 | c.3079C>G (p.Leu1027Val) n.3185C>G | |
| 14 | g.23423567G= | CA2123453044 | MYH7 | c.3079C= (p.Leu1027=) n.3185C= | |
| 14 | g.23423567G>T | CA389045685 | MYH7 | c.3079C>A (p.Leu1027Met) n.3185C>A | gnomAD v4 |
| 14 | g.23423568C>A | CA389045688 | MYH7 | c.3078G>T (p.Lys1026Asn) n.3184G>T | |
| 14 | g.23423568C>G | CA389045689 | MYH7 | c.3078G>C (p.Lys1026Asn) n.3184G>C | |
| 14 | g.23423568C>T | CA485622543 | MYH7 | c.3078G>A (p.Lys1026=) n.3184G>A | |
| 14 | g.23423569T>A | CA389045693 | MYH7 | c.3077A>T (p.Lys1026Met) n.3183A>T | |
| 14 | g.23423569T>C | CA389045692 | MYH7 | c.3077A>G (p.Lys1026Arg) n.3183A>G | |
| 14 | g.23423569T>G | CA389045691 | MYH7 | c.3077A>C (p.Lys1026Thr) n.3183A>C | |
| 14 | g.23423570T>A | CA389045695 | MYH7 | c.3076A>T (p.Lys1026Ter) n.3182A>T | |
| 14 | g.23423570T>C | CA389045697 | MYH7 | c.3076A>G (p.Lys1026Glu) n.3182A>G | |
| 14 | g.23423570T>G | CA389045698 | MYH7 | c.3076A>C (p.Lys1026Gln) n.3182A>C | |
| 14 | g.23423571G>A | CA485622549 | MYH7 | c.3075C>T (p.Val1025=) n.3181C>T | ClinVar |
| 14 | g.23423571G>C | CA485622548 | MYH7 | c.3075C>G (p.Val1025=) n.3181C>G | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23423571G= | CA2123453048 | MYH7 | c.3075C= (p.Val1025=) n.3181C= | |
| 14 | g.23423571G>T | CA485622547 | MYH7 | c.3075C>A (p.Val1025=) n.3181C>A | |
| 14 | g.23423572A>C | CA389045700 | MYH7 | c.3074T>G (p.Val1025Gly) n.3180T>G | |
| 14 | g.23423572A>G | CA389045701 | MYH7 | c.3074T>C (p.Val1025Ala) n.3180T>C | |
| 14 | g.23423572A>T | CA389045702 | MYH7 | c.3074T>A (p.Val1025Asp) n.3180T>A | |
| 14 | g.23423573C>A | CA389045704 | MYH7 | c.3073G>T (p.Val1025Phe) n.3179G>T | |
| 14 | g.23423573C>G | CA389045706 | MYH7 | c.3073G>C (p.Val1025Leu) n.3179G>C | |
| 14 | g.23423573C>T | CA389045707 | MYH7 | c.3073G>A (p.Val1025Ile) n.3179G>A | |
| 14 | g.23423574T>A | CA389045709 | MYH7 | c.3072A>T (p.Lys1024Asn) n.3178A>T | |
| 14 | g.23423574T>C | CA485622553 | MYH7 | c.3072A>G (p.Lys1024=) n.3178A>G | dbSNP |
| 14 | g.23423574T>G | CA389045710 | MYH7 | c.3072A>C (p.Lys1024Asn) n.3178A>C | |
| 14 | g.23423574T= | CA2123453052 | MYH7 | c.3072A= (p.Lys1024=) n.3178A= | |
| 14 | g.23423575T>A | CA389045712 | MYH7 | c.3071A>T (p.Lys1024Ile) n.3177A>T | |
| 14 | g.23423575T>C | CA389045713 | MYH7 | c.3071A>G (p.Lys1024Arg) n.3177A>G | |
| 14 | g.23423575T>G | CA389045714 | MYH7 | c.3071A>C (p.Lys1024Thr) n.3177A>C | |
| 14 | g.23423576T>A | CA389045718 | MYH7 | c.3070A>T (p.Lys1024Ter) n.3176A>T | |
| 14 | g.23423576T>C | CA389045719 | MYH7 | c.3070A>G (p.Lys1024Glu) n.3176A>G | |
| 14 | g.23423576T>G | CA389045716 | MYH7 | c.3070A>C (p.Lys1024Gln) n.3176A>C | |
| 14 | g.23423577G>A | CA485622557 | MYH7 | c.3069C>T (p.Ala1023=) n.3175C>T | |
| 14 | g.23423577G>C | CA485622558 | MYH7 | c.3069C>G (p.Ala1023=) n.3175C>G | |
| 14 | g.23423577G>T | CA485622559 | MYH7 | c.3069C>A (p.Ala1023=) n.3175C>A | |
| 14 | g.23423578G>A | CA035427 | MYH7 | c.3068C>T (p.Ala1023Val) n.3174C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423578G>C | CA389045721 | MYH7 | c.3068C>G (p.Ala1023Gly) n.3174C>G | |
| 14 | g.23423578G= | CA2123453060 | MYH7 | c.3068C= (p.Ala1023=) n.3174C= | |
| 14 | g.23423578G>T | CA389045723 | MYH7 | c.3068C>A (p.Ala1023Asp) n.3174C>A | |
| 14 | g.23423579C>A | CA389045724 | MYH7 | c.3067G>T (p.Ala1023Ser) n.3173G>T | |
| 14 | g.23423579C= | CA2123453073 | MYH7 | c.3067G= (p.Ala1023=) n.3173G= | |
| 14 | g.23423579C>G | CA389045725 | MYH7 | c.3067G>C (p.Ala1023Pro) n.3173G>C | |
| 14 | g.23423579C>T | CA389045726 | MYH7 | c.3067G>A (p.Ala1023Thr) n.3173G>A | ClinVar gnomAD v4 |
| 14 | g.23423580C>A | CA389045729 | MYH7 | c.3066G>T (p.Lys1022Asn) n.3172G>T | |
| 14 | g.23423580C>G | CA389045727 | MYH7 | c.3066G>C (p.Lys1022Asn) n.3172G>C | |
| 14 | g.23423580C>T | CA485622562 | MYH7 | c.3066G>A (p.Lys1022=) n.3172G>A | COSMIC |
| 14 | g.23423581T>A | CA389045731 | MYH7 | c.3065A>T (p.Lys1022Met) n.3171A>T | ClinVar |
| 14 | g.23423581T>C | CA389045733 | MYH7 | c.3065A>G (p.Lys1022Arg) n.3171A>G | |
| 14 | g.23423581T>G | CA389045735 | MYH7 | c.3065A>C (p.Lys1022Thr) n.3171A>C | |
| 14 | g.23423582T>A | CA389045737 | MYH7 | c.3064A>T (p.Lys1022Ter) n.3170A>T | |
| 14 | g.23423582T>C | CA389045738 | MYH7 | c.3064A>G (p.Lys1022Glu) n.3170A>G | ClinVar dbSNP |
| 14 | g.23423582T>G | CA389045739 | MYH7 | c.3064A>C (p.Lys1022Gln) n.3170A>C | |
| 14 | g.23423582T= | CA2123453082 | MYH7 | c.3064A= (p.Lys1022=) n.3170A= | |
| 14 | g.23423583A= | CA2123453085 | MYH7 | c.3063T= (p.Thr1021=) n.3169T= | |
| 14 | g.23423583A>C | CA485622566 | MYH7 | c.3063T>G (p.Thr1021=) n.3169T>G | |
| 14 | g.23423583A>G | CA485622567 | MYH7 | c.3063T>C (p.Thr1021=) n.3169T>C | dbSNP |
| 14 | g.23423583A>T | CA485622568 | MYH7 | c.3063T>A (p.Thr1021=) n.3169T>A | |
| 14 | g.23423584G>A | CA389045741 | MYH7 | c.3062C>T (p.Thr1021Ile) n.3168C>T | ClinVar dbSNP |
| 14 | g.23423584G>C | CA389045744 | MYH7 | c.3062C>G (p.Thr1021Ser) n.3168C>G | |
| 14 | g.23423584G= | CA2123453090 | MYH7 | c.3062C= (p.Thr1021=) n.3168C= | |
| 14 | g.23423584G>T | CA389045743 | MYH7 | c.3062C>A (p.Thr1021Asn) n.3168C>A | |
| 14 | g.23423585T>A | CA389045745 | MYH7 | c.3061A>T (p.Thr1021Ser) n.3167A>T | |
| 14 | g.23423585T>C | CA389045747 | MYH7 | c.3061A>G (p.Thr1021Ala) n.3167A>G | |
| 14 | g.23423585T>G | CA389045748 | MYH7 | c.3061A>C (p.Thr1021Pro) n.3167A>C | |
| 14 | g.23423586C>A | CA485622570 | MYH7 | c.3060G>T (p.Leu1020=) n.3166G>T | |
| 14 | g.23423586C>G | CA485622571 | MYH7 | c.3060G>C (p.Leu1020=) n.3166G>C | COSMIC |
| 14 | g.23423586C>T | CA485622572 | MYH7 | c.3060G>A (p.Leu1020=) n.3166G>A | |
| 14 | g.23423587A>C | CA389045750 | MYH7 | c.3059T>G (p.Leu1020Arg) n.3165T>G | |
| 14 | g.23423587A>G | CA389045752 | MYH7 | c.3059T>C (p.Leu1020Pro) n.3165T>C | |
| 14 | g.23423587A>T | CA389045753 | MYH7 | c.3059T>A (p.Leu1020Gln) n.3165T>A | |
| 14 | g.23423588G>A | CA485622573 | MYH7 | c.3058C>T (p.Leu1020=) n.3164C>T | |
| 14 | g.23423588G>C | CA16614405 | MYH7 | c.3058C>G (p.Leu1020Val) n.3164C>G | ClinVar dbSNP |
| 14 | g.23423588G= | CA2123453100 | MYH7 | c.3058C= (p.Leu1020=) n.3164C= | |
| 14 | g.23423588G>T | CA035407 | MYH7 | c.3058C>A (p.Leu1020Met) n.3164C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423589G>A | CA485622575 | MYH7 | c.3057C>T (p.Thr1019=) n.3163C>T | dbSNP |
| 14 | g.23423589G>C | CA485622576 | MYH7 | c.3057C>G (p.Thr1019=) n.3163C>G | gnomAD v4 |
| 14 | g.23423589G= | CA2123453108 | MYH7 | c.3057C= (p.Thr1019=) n.3163C= | |
| 14 | g.23423589G>T | CA485622577 | MYH7 | c.3057C>A (p.Thr1019=) n.3163C>A | |
| 14 | g.23423590G>A | CA389045756 | MYH7 | c.3056C>T (p.Thr1019Ile) n.3162C>T | |
| 14 | g.23423590G>C | CA389045757 | MYH7 | c.3056C>G (p.Thr1019Ser) n.3162C>G | |
| 14 | g.23423590G= | CA2123453117 | MYH7 | c.3056C= (p.Thr1019=) n.3162C= | |
| 14 | g.23423590G>T | CA013337 | MYH7 | c.3056C>A (p.Thr1019Asn) n.3162C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423591T>A | CA389045758 | MYH7 | c.3055A>T (p.Thr1019Ser) n.3161A>T | |
| 14 | g.23423591T>C | CA013327 | MYH7 | c.3055A>G (p.Thr1019Ala) n.3161A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23423591T>G | CA389045759 | MYH7 | c.3055A>C (p.Thr1019Pro) n.3161A>C | |
| 14 | g.23423591T= | CA2123453128 | MYH7 | c.3055A= (p.Thr1019=) n.3161A= | |
| 14 | g.23423592G>A | CA485622582 | MYH7 | c.3054C>T (p.Asn1018=) n.3160C>T | ClinVar dbSNP |
| 14 | g.23423592G>C | CA389045761 | MYH7 | c.3054C>G (p.Asn1018Lys) n.3160C>G | |
| 14 | g.23423592G= | CA2123453134 | MYH7 | c.3054C= (p.Asn1018=) n.3160C= | |
| 14 | g.23423592G>T | CA389045762 | MYH7 | c.3054C>A (p.Asn1018Lys) n.3160C>A | |
| 14 | g.23423593T>A | CA389045764 | MYH7 | c.3053A>T (p.Asn1018Ile) n.3159A>T | |
| 14 | g.23423593T>C | CA389045765 | MYH7 | c.3053A>G (p.Asn1018Ser) n.3159A>G | |
| 14 | g.23423593T>G | CA389045767 | MYH7 | c.3053A>C (p.Asn1018Thr) n.3159A>C | |
| 14 | g.23423594T>A | CA389045769 | MYH7 | c.3052A>T (p.Asn1018Tyr) n.3158A>T | |
| 14 | g.23423594T>C | CA389045770 | MYH7 | c.3052A>G (p.Asn1018Asp) n.3158A>G | |
| 14 | g.23423594T>G | CA389045771 | MYH7 | c.3052A>C (p.Asn1018His) n.3158A>C | |
| 14 | g.23423595G>A | CA485622585 | MYH7 | c.3051C>T (p.Val1017=) n.3157C>T | ClinVar dbSNP |
| 14 | g.23423595G>C | CA485622586 | MYH7 | c.3051C>G (p.Val1017=) n.3157C>G | |
| 14 | g.23423595G= | CA2123453146 | MYH7 | c.3051C= (p.Val1017=) n.3157C= | |
| 14 | g.23423595G>T | CA485622587 | MYH7 | c.3051C>A (p.Val1017=) n.3157C>A | |
| 14 | g.23423596A= | CA2123453150 | MYH7 | c.3050T= (p.Val1017=) n.3156T= | |
| 14 | g.23423596A>C | CA389045772 | MYH7 | c.3050T>G (p.Val1017Gly) n.3156T>G | |
| 14 | g.23423596A>G | CA035382 | MYH7 | c.3050T>C (p.Val1017Ala) n.3156T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23423596A>T | CA389045774 | MYH7 | c.3050T>A (p.Val1017Asp) n.3156T>A | |
| 14 | g.23423597C>A | CA389045777 | MYH7 | c.3049G>T (p.Val1017Phe) n.3155G>T | |
| 14 | g.23423597C>G | CA389045778 | MYH7 | c.3049G>C (p.Val1017Leu) n.3155G>C | |
| 14 | g.23423597C>T | CA389045779 | MYH7 | c.3049G>A (p.Val1017Ile) n.3155G>A | ClinVar |
| 14 | g.23423598C>A | CA389045782 | MYH7 | c.3048G>T (p.Lys1016Asn) n.3154G>T | |
| 14 | g.23423598C>G | CA389045780 | MYH7 | c.3048G>C (p.Lys1016Asn) n.3154G>C | |
| 14 | g.23423598C>T | CA485622592 | MYH7 | c.3048G>A (p.Lys1016=) n.3154G>A | ClinVar gnomAD v4 |
| 14 | g.23423599T>A | CA389045784 | MYH7 | c.3047A>T (p.Lys1016Met) n.3153A>T | |
| 14 | g.23423599T>C | CA389045785 | MYH7 | c.3047A>G (p.Lys1016Arg) n.3153A>G | |
| 14 | g.23423599T>G | CA389045786 | MYH7 | c.3047A>C (p.Lys1016Thr) n.3153A>C | |
| 14 | g.23423600T>A | CA389045788 | MYH7 | c.3046A>T (p.Lys1016Ter) n.3152A>T | |
| 14 | g.23423600T>C | CA035369 | MYH7 | c.3046A>G (p.Lys1016Glu) n.3152A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23423600T>G | CA389045790 | MYH7 | c.3046A>C (p.Lys1016Gln) n.3152A>C | |
| 14 | g.23423600T= | CA2123453156 | MYH7 | c.3046A= (p.Lys1016=) n.3152A= | |
| 14 | g.23423601G>A | CA035354 | MYH7 | c.3045C>T (p.Asp1015=) n.3151C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423601G>C | CA389045792 | MYH7 | c.3045C>G (p.Asp1015Glu) n.3151C>G | |
| 14 | g.23423601G= | CA2123453159 | MYH7 | c.3045C= (p.Asp1015=) n.3151C= | |
| 14 | g.23423601G>T | CA389045793 | MYH7 | c.3045C>A (p.Asp1015Glu) n.3151C>A | |
| 14 | g.23423602T>A | CA389045795 | MYH7 | c.3044A>T (p.Asp1015Val) n.3150A>T | |
| 14 | g.23423602T>C | CA389045797 | MYH7 | c.3044A>G (p.Asp1015Gly) n.3150A>G | gnomAD v4 |
| 14 | g.23423602T>G | CA389045798 | MYH7 | c.3044A>C (p.Asp1015Ala) n.3150A>C | |
| 14 | g.23423603C>A | CA389045802 | MYH7 | c.3043G>T (p.Asp1015Tyr) n.3149G>T | |
| 14 | g.23423603C>G | CA389045801 | MYH7 | c.3043G>C (p.Asp1015His) n.3149G>C | |
| 14 | g.23423603C>T | CA389045800 | MYH7 | c.3043G>A (p.Asp1015Asn) n.3149G>A | |
| 14 | g.23423604C>A | CA389045804 | MYH7 | c.3042G>T (p.Glu1014Asp) n.3148G>T | |
| 14 | g.23423604C= | CA2123453166 | MYH7 | c.3042G= (p.Glu1014=) n.3148G= | |
| 14 | g.23423604C>G | CA389045805 | MYH7 | c.3042G>C (p.Glu1014Asp) n.3148G>C | |
| 14 | g.23423604C>T | CA485622596 | MYH7 | c.3042G>A (p.Glu1014=) n.3148G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23423605T>A | CA389045807 | MYH7 | c.3041A>T (p.Glu1014Val) n.3147A>T | gnomAD v4 |
| 14 | g.23423605T>C | CA389045808 | MYH7 | c.3041A>G (p.Glu1014Gly) n.3147A>G | |
| 14 | g.23423605T>G | CA389045809 | MYH7 | c.3041A>C (p.Glu1014Ala) n.3147A>C | |
| 14 | g.23423606C>A | CA389045811 | MYH7 | c.3040G>T (p.Glu1014Ter) n.3146G>T | |
| 14 | g.23423606C= | CA2123453170 | MYH7 | c.3040G= (p.Glu1014=) n.3146G= | |
| 14 | g.23423606C>G | CA389045812 | MYH7 | c.3040G>C (p.Glu1014Gln) n.3146G>C | |
| 14 | g.23423606C>T | CA035343 | MYH7 | c.3040G>A (p.Glu1014Lys) n.3146G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23423607C>A | CA257818711 | MYH7 | c.3039G>T (p.Glu1013Asp) n.3145G>T | dbSNP |
| 14 | g.23423607C= | CA2123453173 | MYH7 | c.3039G= (p.Glu1013=) n.3145G= | |
| 14 | g.23423607C>G | CA389045815 | MYH7 | c.3039G>C (p.Glu1013Asp) n.3145G>C | |
| 14 | g.23423607C>T | CA485622598 | MYH7 | c.3039G>A (p.Glu1013=) n.3145G>A | |
| 14 | g.23423608T>A | CA389045817 | MYH7 | c.3038A>T (p.Glu1013Val) n.3144A>T | |
| 14 | g.23423608T>C | CA389045818 | MYH7 | c.3038A>G (p.Glu1013Gly) n.3144A>G | gnomAD v4 |
| 14 | g.23423608T>G | CA389045820 | MYH7 | c.3038A>C (p.Glu1013Ala) n.3144A>C | |
| 14 | g.23423609C>A | CA389045822 | MYH7 | c.3037G>T (p.Glu1013Ter) n.3143G>T | gnomAD v4 |
| 14 | g.23423609C= | CA2123453182 | MYH7 | c.3037G= (p.Glu1013=) n.3143G= | |
| 14 | g.23423609C>G | CA389045821 | MYH7 | c.3037G>C (p.Glu1013Gln) n.3143G>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23423609C>T | CA013322 | MYH7 | c.3037G>A (p.Glu1013Lys) n.3143G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23423610G>A | CA013313 | MYH7 | c.3036C>T (p.Ala1012=) n.3142C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423610G>C | CA485622599 | MYH7 | c.3036C>G (p.Ala1012=) n.3142C>G | |
| 14 | g.23423610G= | CA2123453193 | MYH7 | c.3036C= (p.Ala1012=) n.3142C= | |
| 14 | g.23423610G>T | CA485622600 | MYH7 | c.3036C>A (p.Ala1012=) n.3142C>A | gnomAD v4 |
| 14 | g.23423611G>A | CA389045824 | MYH7 | c.3035C>T (p.Ala1012Val) n.3141C>T | gnomAD v4 |
| 14 | g.23423611G>C | CA389045825 | MYH7 | c.3035C>G (p.Ala1012Gly) n.3141C>G | |
| 14 | g.23423611G= | CA2123453203 | MYH7 | c.3035C= (p.Ala1012=) n.3141C= | |
| 14 | g.23423611G>T | CA035299 | MYH7 | c.3035C>A (p.Ala1012Asp) n.3141C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23423612C>A | CA389045828 | MYH7 | c.3034G>T (p.Ala1012Ser) n.3140G>T | |
| 14 | g.23423612C>G | CA389045829 | MYH7 | c.3034G>C (p.Ala1012Pro) n.3140G>C | |
| 14 | g.23423612C>T | CA389045830 | MYH7 | c.3034G>A (p.Ala1012Thr) n.3140G>A | ClinVar |
| 14 | g.23423613C>A | CA389045831 | MYH7 | c.3033G>T (p.Gln1011His) n.3139G>T | |
| 14 | g.23423613C>G | CA389045832 | MYH7 | c.3033G>C (p.Gln1011His) n.3139G>C | |
| 14 | g.23423613C>T | CA485622601 | MYH7 | c.3033G>A (p.Gln1011=) n.3139G>A | COSMIC |
| 14 | g.23423614T>A | CA389045834 | MYH7 | c.3032A>T (p.Gln1011Leu) n.3138A>T | |
| 14 | g.23423614T>C | CA389045836 | MYH7 | c.3032A>G (p.Gln1011Arg) n.3138A>G | |
| 14 | g.23423614T>G | CA389045837 | MYH7 | c.3032A>C (p.Gln1011Pro) n.3138A>C | |
| 14 | g.23423615G>A | CA389045842 | MYH7 | c.3031C>T (p.Gln1011Ter) n.3137C>T | |
| 14 | g.23423615G>C | CA389045844 | MYH7 | c.3031C>G (p.Gln1011Glu) n.3137C>G | |
| 14 | g.23423615G>T | CA389045840 | MYH7 | c.3031C>A (p.Gln1011Lys) n.3137C>A | |
| 14 | g.23423616A= | CA2123453207 | MYH7 | c.3030T= (p.Leu1010=) n.3136T= | |
| 14 | g.23423616A>C | CA035281 | MYH7 | c.3030T>G (p.Leu1010=) n.3136T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23423616A>G | CA485622603 | MYH7 | c.3030T>C (p.Leu1010=) n.3136T>C | |
| 14 | g.23423616A>T | CA485622602 | MYH7 | c.3030T>A (p.Leu1010=) n.3136T>A | |
| 14 | g.23423617A>C | CA389045846 | MYH7 | c.3029T>G (p.Leu1010Arg) n.3135T>G | |
| 14 | g.23423617A>G | CA389045849 | MYH7 | c.3029T>C (p.Leu1010Pro) n.3135T>C | |
| 14 | g.23423617A>T | CA389045848 | MYH7 | c.3029T>A (p.Leu1010His) n.3135T>A | |
| 14 | g.23423618G>A | CA035267 | MYH7 | c.3028C>T (p.Leu1010Phe) n.3134C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423618G>C | CA389045852 | MYH7 | c.3028C>G (p.Leu1010Val) n.3134C>G | |
| 14 | g.23423618G= | CA2123453211 | MYH7 | c.3028C= (p.Leu1010=) n.3134C= | |
| 14 | g.23423618G>T | CA389045851 | MYH7 | c.3028C>A (p.Leu1010Ile) n.3134C>A | |
| 14 | g.23423619G>A | CA485622604 | MYH7 | c.3027C>T (p.Asp1009=) n.3133C>T | |
| 14 | g.23423619G>C | CA389045853 | MYH7 | c.3027C>G (p.Asp1009Glu) n.3133C>G | |
| 14 | g.23423619G>T | CA389045854 | MYH7 | c.3027C>A (p.Asp1009Glu) n.3133C>A | |
| 14 | g.23423620T>A | CA389045856 | MYH7 | c.3026A>T (p.Asp1009Val) n.3132A>T | |
| 14 | g.23423620T>C | CA389045859 | MYH7 | c.3026A>G (p.Asp1009Gly) n.3132A>G | ClinVar dbSNP |
| 14 | g.23423620T>G | CA389045858 | MYH7 | c.3026A>C (p.Asp1009Ala) n.3132A>C | |
| 14 | g.23423620T= | CA2123453214 | MYH7 | c.3026A= (p.Asp1009=) n.3132A= | |
| 14 | g.23423621C>A | CA389045860 | MYH7 | c.3025G>T (p.Asp1009Tyr) n.3131G>T | |
| 14 | g.23423621C>G | CA389045862 | MYH7 | c.3025G>C (p.Asp1009His) n.3131G>C | |
| 14 | g.23423621C>T | CA389045863 | MYH7 | c.3025G>A (p.Asp1009Asn) n.3131G>A | gnomAD v4 |
| 14 | g.23423622A>C | CA389045865 | MYH7 | c.3024T>G (p.Asp1008Glu) n.3130T>G | |
| 14 | g.23423622A>G | CA485622605 | MYH7 | c.3024T>C (p.Asp1008=) n.3130T>C | |
| 14 | g.23423622A>T | CA389045866 | MYH7 | c.3024T>A (p.Asp1008Glu) n.3130T>A | |
| 14 | g.23423623T>A | CA389045868 | MYH7 | c.3023A>T (p.Asp1008Val) n.3129A>T | ClinVar |
| 14 | g.23423623T>C | CA389045869 | MYH7 | c.3023A>G (p.Asp1008Gly) n.3129A>G | gnomAD v4 |
| 14 | g.23423623T>G | CA389045870 | MYH7 | c.3023A>C (p.Asp1008Ala) n.3129A>C | |
| 14 | g.23423624C>A | CA389045872 | MYH7 | c.3022G>T (p.Asp1008Tyr) n.3128G>T | |
| 14 | g.23423624C>G | CA389045873 | MYH7 | c.3022G>C (p.Asp1008His) n.3128G>C | ClinVar |
| 14 | g.23423624C>T | CA389045875 | MYH7 | c.3022G>A (p.Asp1008Asn) n.3128G>A | |
| 14 | g.23423625C>A | CA485622606 | MYH7 | c.3021G>T (p.Leu1007=) n.3127G>T | |
| 14 | g.23423625C= | CA2123453239 | MYH7 | c.3021G= (p.Leu1007=) n.3127G= | |
| 14 | g.23423625C>G | CA485622607 | MYH7 | c.3021G>C (p.Leu1007=) n.3127G>C | |
| 14 | g.23423625C>T | CA485622608 | MYH7 | c.3021G>A (p.Leu1007=) n.3127G>A | dbSNP |
| 14 | g.23423626A= | CA2123453247 | MYH7 | c.3020T= (p.Leu1007=) n.3126T= | |
| 14 | g.23423626A>C | CA389045878 | MYH7 | c.3020T>G (p.Leu1007Arg) n.3126T>G | |
| 14 | g.23423626A>G | CA013309 | MYH7 | c.3020T>C (p.Leu1007Pro) n.3126T>C | ClinVar dbSNP |
| 14 | g.23423626A>T | CA389045877 | MYH7 | c.3020T>A (p.Leu1007Gln) n.3126T>A | |
| 14 | g.23423627G>A | CA485622609 | MYH7 | c.3019C>T (p.Leu1007=) n.3125C>T | |
| 14 | g.23423627G>C | CA389045880 | MYH7 | c.3019C>G (p.Leu1007Val) n.3125C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23423627G= | CA2123453251 | MYH7 | c.3019C= (p.Leu1007=) n.3125C= | |
| 14 | g.23423627G>T | CA389045881 | MYH7 | c.3019C>A (p.Leu1007Met) n.3125C>A | |
| 14 | g.23423628A= | CA2123453260 | MYH7 | c.3018T= (p.Ala1006=) n.3124T= | |
| 14 | g.23423628A>C | CA485622610 | MYH7 | c.3018T>G (p.Ala1006=) n.3124T>G | |
| 14 | g.23423628A>G | CA485622611 | MYH7 | c.3018T>C (p.Ala1006=) n.3124T>C | dbSNP |
| 14 | g.23423628A>T | CA485622612 | MYH7 | c.3018T>A (p.Ala1006=) n.3124T>A | |
| 14 | g.23423629G>A | CA389045883 | MYH7 | c.3017C>T (p.Ala1006Val) n.3123C>T | gnomAD v4 |
| 14 | g.23423629G>C | CA389045885 | MYH7 | c.3017C>G (p.Ala1006Gly) n.3123C>G | |
| 14 | g.23423629G>T | CA389045886 | MYH7 | c.3017C>A (p.Ala1006Asp) n.3123C>A | |
| 14 | g.23423630C>A | CA389045887 | MYH7 | c.3016G>T (p.Ala1006Ser) n.3122G>T | |
| 14 | g.23423630C= | CA2123453263 | MYH7 | c.3016G= (p.Ala1006=) n.3122G= | |
| 14 | g.23423630C>G | CA389045888 | MYH7 | c.3016G>C (p.Ala1006Pro) n.3122G>C | |
| 14 | g.23423630C>T | CA389045889 | MYH7 | c.3016G>A (p.Ala1006Thr) n.3122G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23423631C>A | CA389045891 | MYH7 | c.3015G>T (p.Gln1005His) n.3121G>T | |
| 14 | g.23423631C= | CA2123453270 | MYH7 | c.3015G= (p.Gln1005=) n.3121G= | |
| 14 | g.23423631C>G | CA389045893 | MYH7 | c.3015G>C (p.Gln1005His) n.3121G>C | gnomAD v4 |
| 14 | g.23423631C>T | CA485622613 | MYH7 | c.3015G>A (p.Gln1005=) n.3121G>A | dbSNP gnomAD v4 |
| 14 | g.23423631_23423656dup | CA2729049680 | MYH7 | c.2990_3015dup (p.Ala1006LysfsTer24) n.3096_3121dup | dbSNP |
| 14 | g.23423632T>A | CA389045897 | MYH7 | c.3014A>T (p.Gln1005Leu) n.3120A>T | |
| 14 | g.23423632T>C | CA389045896 | MYH7 | c.3014A>G (p.Gln1005Arg) n.3120A>G | gnomAD v4 |
| 14 | g.23423632T>G | CA389045895 | MYH7 | c.3014A>C (p.Gln1005Pro) n.3120A>C | |
| 14 | g.23423633G>A | CA389045898 | MYH7 | c.3013C>T (p.Gln1005Ter) n.3119C>T | |
| 14 | g.23423633G>C | CA389045900 | MYH7 | c.3013C>G (p.Gln1005Glu) n.3119C>G | ClinVar dbSNP gnomAD v4 |
| 14 | g.23423633G= | CA2123453275 | MYH7 | c.3013C= (p.Gln1005=) n.3119C= | |
| 14 | g.23423633G>T | CA389045901 | MYH7 | c.3013C>A (p.Gln1005Lys) n.3119C>A | |
| 14 | g.23423634T>A | CA389045903 | MYH7 | c.3012A>T (p.Gln1004His) n.3118A>T | |
| 14 | g.23423634T>C | CA035254 | MYH7 | c.3012A>G (p.Gln1004=) n.3118A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423634T>G | CA389045905 | MYH7 | c.3012A>C (p.Gln1004His) n.3118A>C | |
| 14 | g.23423634T= | CA2123453280 | MYH7 | c.3012A= (p.Gln1004=) n.3118A= | |
| 14 | g.23423635T>A | CA389045906 | MYH7 | c.3011A>T (p.Gln1004Leu) n.3117A>T | |
| 14 | g.23423635T>C | CA389045908 | MYH7 | c.3011A>G (p.Gln1004Arg) n.3117A>G | |
| 14 | g.23423635T>G | CA389045909 | MYH7 | c.3011A>C (p.Gln1004Pro) n.3117A>C | |
| 14 | g.23423636G>A | CA389045911 | MYH7 | c.3010C>T (p.Gln1004Ter) n.3116C>T | |
| 14 | g.23423636G>C | CA013300 | MYH7 | c.3010C>G (p.Gln1004Glu) n.3116C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423636G= | CA2123453284 | MYH7 | c.3010C= (p.Gln1004=) n.3116C= | |
| 14 | g.23423636G>T | CA389045913 | MYH7 | c.3010C>A (p.Gln1004Lys) n.3116C>A | |
| 14 | g.23423637G>A | CA485622614 | MYH7 | c.3009C>T (p.His1003=) n.3115C>T | |
| 14 | g.23423637G>C | CA389045915 | MYH7 | c.3009C>G (p.His1003Gln) n.3115C>G | |
| 14 | g.23423637G>T | CA389045914 | MYH7 | c.3009C>A (p.His1003Gln) n.3115C>A | |
| 14 | g.23423638T>A | CA389045917 | MYH7 | c.3008A>T (p.His1003Leu) n.3114A>T | |
| 14 | g.23423638T>C | CA389045919 | MYH7 | c.3008A>G (p.His1003Arg) n.3114A>G | |
| 14 | g.23423638T>G | CA389045921 | MYH7 | c.3008A>C (p.His1003Pro) n.3114A>C | |
| 14 | g.23423639G>A | CA389045922 | MYH7 | c.3007C>T (p.His1003Tyr) n.3113C>T | ClinVar |
| 14 | g.23423639G>C | CA389045923 | MYH7 | c.3007C>G (p.His1003Asp) n.3113C>G | |
| 14 | g.23423639G>T | CA389045925 | MYH7 | c.3007C>A (p.His1003Asn) n.3113C>A | |
| 14 | g.23423640G>A | CA16606535 | MYH7 | c.3006C>T (p.Ala1002=) n.3112C>T | ClinVar dbSNP gnomAD v4 COSMIC |
| 14 | g.23423640G>C | CA485622615 | MYH7 | c.3006C>G (p.Ala1002=) n.3112C>G | |
| 14 | g.23423640G= | CA2123453288 | MYH7 | c.3006C= (p.Ala1002=) n.3112C= | |
| 14 | g.23423640G>T | CA485622616 | MYH7 | c.3006C>A (p.Ala1002=) n.3112C>A | |
| 14 | g.23423641G>A | CA035198 | MYH7 | c.3005C>T (p.Ala1002Val) n.3111C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423641G>C | CA389045928 | MYH7 | c.3005C>G (p.Ala1002Gly) n.3111C>G | |
| 14 | g.23423641G= | CA2123453294 | MYH7 | c.3005C= (p.Ala1002=) n.3111C= | |
| 14 | g.23423641G>T | CA389045929 | MYH7 | c.3005C>A (p.Ala1002Asp) n.3111C>A | |
| 14 | g.23423642C>A | CA389045930 | MYH7 | c.3004G>T (p.Ala1002Ser) n.3110G>T | gnomAD v4 |
| 14 | g.23423642C>G | CA389045931 | MYH7 | c.3004G>C (p.Ala1002Pro) n.3110G>C | |
| 14 | g.23423642C>T | CA389045933 | MYH7 | c.3004G>A (p.Ala1002Thr) n.3110G>A | COSMIC |
| 14 | g.23423643C>A | CA389046260 | MYH7 | c.3003G>T (p.Glu1001Asp) n.3109G>T | |
| 14 | g.23423643C= | CA2123453298 | MYH7 | c.3003G= (p.Glu1001=) n.3109G= | |
| 14 | g.23423643C>G | CA389046262 | MYH7 | c.3003G>C (p.Glu1001Asp) n.3109G>C | |
| 14 | g.23423643C>T | CA257818736 | MYH7 | c.3003G>A (p.Glu1001=) n.3109G>A | dbSNP gnomAD v4 |
| 14 | g.23423644T>A | CA389046266 | MYH7 | c.3002A>T (p.Glu1001Val) n.3108A>T | |
| 14 | g.23423644T>C | CA389046264 | MYH7 | c.3002A>G (p.Glu1001Gly) n.3108A>G | |
| 14 | g.23423644T>G | CA389046265 | MYH7 | c.3002A>C (p.Glu1001Ala) n.3108A>C | |
| 14 | g.23423645C>A | CA389046268 | MYH7 | c.3001G>T (p.Glu1001Ter) n.3107G>T | |
| 14 | g.23423645C>G | CA389046269 | MYH7 | c.3001G>C (p.Glu1001Gln) n.3107G>C | |
| 14 | g.23423645C>T | CA389046271 | MYH7 | c.3001G>A (p.Glu1001Lys) n.3107G>A | gnomAD v4 |
| 14 | g.23423646T>A | CA389046273 | MYH7 | c.3000A>T (p.Gln1000His) n.3106A>T | |
| 14 | g.23423646T>C | CA485766575 | MYH7 | c.3000A>G (p.Gln1000=) n.3106A>G | |
| 14 | g.23423646T>G | CA389046274 | MYH7 | c.3000A>C (p.Gln1000His) n.3106A>C | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23423646T= | CA2123453302 | MYH7 | c.3000A= (p.Gln1000=) n.3106A= |