KIF26B | Mutation | Missense | ENST00000407071.2 |
g.245772763C>T
|
c.1847C>T
|
p.Thr616Met
|
probably damaging
| HepG2 |
KIF26B | Mutation | Missense | ENST00000407071.2 |
g.245847603C>T
|
c.2327C>T
|
p.Ala776Val
|
probably damaging
| HepaRG |
KIF26B | Mutation | Missense | ENST00000407071.2 |
g.245772666A>C
|
c.1750A>C
|
p.Lys584Gln
|
probably damaging
| Huh7 |
KIF26B | Mutation | Missense | ENST00000407071.2 |
g.245318753G>C
|
c.27G>C
|
p.Glu9Asp
|
benign
| Mahlavu |
KIF26B | Mutation | Missense | ENST00000407071.2 |
g.245849089G>T
|
c.2804G>T
|
p.Cys935Phe
|
probably damaging
| Li7 |
KIF26B | Mutation | Missense | ENST00000407071.2 |
g.245850456A>G
|
c.4171A>G
|
p.Ile1391Val
|
benign
| JHH6 |