TNNI3K | Mutation | Missense | ENST00000326637.3 |
g.74902193A>T
|
c.1861A>T
|
p.Met722Leu
|
benign
| SNU182 |
TNNI3K | Mutation | Missense | ENST00000326637.3 |
g.74737384C>A
|
c.436C>A
|
p.His247Asn
|
benign
| PLC.PRF5 |
TNNI3K | Mutation | Missense | ENST00000326637.3 |
g.74905204A>T
|
c.1909A>T
|
p.Thr738Ser
|
benign
| HLE |
TNNI3K | Mutation | Missense | ENST00000326637.3 |
g.74905204A>T
|
c.1909A>T
|
p.Thr738Ser
|
benign
| HLF |
TNNI3K | Mutation | Truncating | ENST00000326637.3 |
g.75009591C>A
|
c.2433C>A
|
p.Gly811Gly (Splice)
|
damaging
| HCC.1.2 |
TNNI3K | Mutation | Truncating | ENST00000326637.3 |
g.74902213T>C
|
c.1878+3T>C
|
p.?
|
damaging
| SNU449 |