Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 |