| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23431620_23433131dup | CA3267438993 | MYH7 | c.298_697dup n.404_803dup | |
| 14 | g.23433118T>A | CA389053126 | MYH7 | c.311A>T (p.Asn104Ile) n.417A>T | |
| 14 | g.23433118T>C | CA389053128 | MYH7 | c.311A>G (p.Asn104Ser) n.417A>G | ClinVar dbSNP gnomAD v4 |
| 14 | g.23433118T>G | CA389053129 | MYH7 | c.311A>C (p.Asn104Thr) n.417A>C | |
| 14 | g.23433118T= | CA2123454840 | MYH7 | c.311A= (p.Asn104=) n.417A= | dbSNP |
| 14 | g.23433119T>A | CA389053130 | MYH7 | c.310A>T (p.Asn104Tyr) n.416A>T | |
| 14 | g.23433119T>C | CA389053132 | MYH7 | c.310A>G (p.Asn104Asp) n.416A>G | COSMIC |
| 14 | g.23433119T>G | CA389053134 | MYH7 | c.310A>C (p.Asn104His) n.416A>C | |
| 14 | g.23433120G>A | CA485626711 | MYH7 | c.309C>T (p.Tyr103=) n.415C>T | |
| 14 | g.23433120G>C | CA389053137 | MYH7 | c.309C>G (p.Tyr103Ter) n.415C>G | |
| 14 | g.23433120G>T | CA389053135 | MYH7 | c.309C>A (p.Tyr103Ter) n.415C>A | |
| 14 | g.23433121T>A | CA389053139 | MYH7 | c.308A>T (p.Tyr103Phe) n.414A>T | |
| 14 | g.23433121T>C | CA389053141 | MYH7 | c.308A>G (p.Tyr103Cys) n.414A>G | ClinVar dbSNP |
| 14 | g.23433121T>G | CA389053142 | MYH7 | c.308A>C (p.Tyr103Ser) n.414A>C | |
| 14 | g.23433121T= | CA3207920896 | MYH7 | c.308A= (p.Tyr103=) n.414A= | dbSNP |
| 14 | g.23433122A= | CA3207920903 | MYH7 | c.307T= (p.Tyr103=) n.413T= | dbSNP |
| 14 | g.23433122A>C | CA389053143 | MYH7 | c.307T>G (p.Tyr103Asp) n.413T>G | |
| 14 | g.23433122A>G | CA389053144 | MYH7 | c.307T>C (p.Tyr103His) n.413T>C | dbSNP gnomAD v4 |
| 14 | g.23433122A>T | CA389053146 | MYH7 | c.307T>A (p.Tyr103Asn) n.413T>A | |
| 14 | g.23433123G>A | CA485626722 | MYH7 | c.306C>T (p.Leu102=) n.412C>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23433123G>C | CA485626724 | MYH7 | c.306C>G (p.Leu102=) n.412C>G | |
| 14 | g.23433123G= | CA3209385321 | MYH7 | c.306C= (p.Leu102=) n.412C= | dbSNP |
| 14 | g.23433123G>T | CA485626726 | MYH7 | c.306C>A (p.Leu102=) n.412C>A | |
| 14 | g.23433124A>C | CA389053148 | MYH7 | c.305T>G (p.Leu102Arg) n.411T>G | |
| 14 | g.23433124A>G | CA389053150 | MYH7 | c.305T>C (p.Leu102Pro) n.411T>C | COSMIC |
| 14 | g.23433124A>T | CA389053149 | MYH7 | c.305T>A (p.Leu102His) n.411T>A | |
| 14 | g.23433125G>A | CA389053152 | MYH7 | c.304C>T (p.Leu102Phe) n.410C>T | dbSNP gnomAD v4 |
| 14 | g.23433125G>C | CA389053153 | MYH7 | c.304C>G (p.Leu102Val) n.410C>G | dbSNP gnomAD v4 |
| 14 | g.23433125G= | CA3209385332 | MYH7 | c.304C= (p.Leu102=) n.410C= | dbSNP |
| 14 | g.23433125G>T | CA389053155 | MYH7 | c.304C>A (p.Leu102Ile) n.410C>A | |
| 14 | g.23433126C>A | CA485626735 | MYH7 | c.303G>T (p.Val101=) n.409G>T | |
| 14 | g.23433126C>G | CA485626738 | MYH7 | c.303G>C (p.Val101=) n.409G>C | |
| 14 | g.23433126C>T | CA485626737 | MYH7 | c.303G>A (p.Val101=) n.409G>A | gnomAD v4 |
| 14 | g.23433127A>C | CA389053156 | MYH7 | c.302T>G (p.Val101Gly) n.408T>G | |
| 14 | g.23433127A>G | CA389053158 | MYH7 | c.302T>C (p.Val101Ala) n.408T>C | |
| 14 | g.23433127A>T | CA389053160 | MYH7 | c.302T>A (p.Val101Glu) n.408T>A | |
| 14 | g.23433128C>A | CA389053162 | MYH7 | c.301G>T (p.Val101Leu) n.407G>T | |
| 14 | g.23433128C>G | CA389053163 | MYH7 | c.301G>C (p.Val101Leu) n.407G>C | |
| 14 | g.23433128C>T | CA389053165 | MYH7 | c.301G>A (p.Val101Met) n.407G>A | |
| 14 | g.23433129C>A | CA485626748 | MYH7 | c.300G>T (p.Ala100=) n.406G>T | ClinVar dbSNP |
| 14 | g.23433129C= | CA2123454846 | MYH7 | c.300G= (p.Ala100=) n.406G= | dbSNP |
| 14 | g.23433129C>G | CA485626749 | MYH7 | c.300G>C (p.Ala100=) n.406G>C | dbSNP gnomAD v4 |
| 14 | g.23433129C>T | CA035215 | MYH7 | c.300G>A (p.Ala100=) n.406G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23433130G>A | CA10576964 | MYH7 | c.299C>T (p.Ala100Val) n.405C>T | ClinVar dbSNP |
| 14 | g.23433130G>C | CA389053169 | MYH7 | c.299C>G (p.Ala100Gly) n.405C>G | |
| 14 | g.23433130G= | CA2123454852 | MYH7 | c.299C= (p.Ala100=) n.405C= | dbSNP |
| 14 | g.23433130G>T | CA389053168 | MYH7 | c.299C>A (p.Ala100Glu) n.405C>A | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23433131C>A | CA035151 | MYH7 | c.298G>T (p.Ala100Ser) n.404G>T | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23433131C= | CA2123454861 | MYH7 | c.298G= (p.Ala100=) n.404G= | dbSNP |
| 14 | g.23433131C>G | CA389053172 | MYH7 | c.298G>C (p.Ala100Pro) n.404G>C |