| 基因名 | 突变 |
|---|---|
| TTN(NM_001267550,titin,35991aa) | g.2:179404402T>C,c.98390A>G,p.N32797S |
| TTN(NM_001267550,titin,35991aa) | g.2:179404310T>C,c.98482A>G,p.I32828V |
| TTN(NM_001267550,titin,35991aa) | g.2:179404187G>A,c.98605C>T,p.R32869C |
| TTN(NM_001267550,titin,35991aa) | g.2:179404151G>A,c.98641C>T,p.P32881S |
| TTN(NM_001267550,titin,35991aa) | g.2:179403946C>T,c.98716G>A,p.V32906I |
| TTN(NM_001267550,titin,35991aa) | g.2:179403936A>G,c.98726T>C,p.V32909A |
| TTN(NM_001267550,titin,35991aa) | g.2:179403750C>T,c.98912G>A,p.R32971H |
| TTN(NM_001267550,titin,35991aa) | g.2:179403525A>T,c.99031T>A,p.S33011T |
| TTN(NM_001267550,titin,35991aa) | g.2:179402266C>T,c.99668G>A,p.R33223H |
| TTN(NM_001267550,titin,35991aa) | g.2:179401787G>A,c.100049C>T,p.T33350I |
| TTN(NM_001267550,titin,35991aa) | g.2:179401778A>G,c.100058T>C,p.I33353T |
| TTN(NM_001267550,titin,35991aa) | g.2:179401742C>T,c.100094G>A,p.R33365Q |
| TTN(NM_001267550,titin,35991aa) | g.2:179401740C>T,c.100096G>A,p.V33366I |
| TTN(NM_001267550,titin,35991aa) | g.2:179401179C>T,c.100295G>A,p.R33432H |
| TTN(NM_001267550,titin,35991aa) | g.2:179401078G>A,c.100396C>T,p.R33466C |
| TTN(NM_001267550,titin,35991aa) | g.2:179400895C>T,c.100579G>A,p.V33527I |
| TTN(NM_001267550,titin,35991aa) | g.2:179400130G>A,c.101212C>T,p.R33738C |
| TTN(NM_001267550,titin,35991aa) | g.2:179399964T>A,c.101378A>T,p.D33793V |
| TTN(NM_001267550,titin,35991aa) | g.2:179399743G>C,c.101599C>G,p.L33867V |
| TTN(NM_001267550,titin,35991aa) | g.2:179399677C>T,c.101665G>A,p.V33889I |
| TTN(NM_001267550,titin,35991aa) | g.2:179399634C>T,c.101708G>A,p.R33903H |
| TTN(NM_001267550,titin,35991aa) | g.2:179399576C>G,c.101766G>C,p.Q33922H |
| TTN(NM_001267550,titin,35991aa) | g.2:179399451C>T,c.101891G>A,p.R33964H |
| TTN(NM_001267550,titin,35991aa) | g.2:179398818C>T,c.102524G>A,p.R34175Q |
| TTN(NM_001267550,titin,35991aa) | g.2:179398747T>C,c.102595A>G,p.I34199V |
| TTN(NM_001267550,titin,35991aa) | g.2:179398605C>T,c.102737G>A,p.R34246H |
| TTN(NM_001267550,titin,35991aa) | g.2:179398509C>A,c.102833G>T,p.G34278V |
| TTN(NM_001267550,titin,35991aa) | g.2:179398195C>G,c.103147G>C,p.E34383Q |