ATM | Mutation | Missense | ENST00000278616.4 |
g.108224537G>A
|
c.8716G>A
|
p.Val2906Ile
|
probably damaging
| HepG2 |
ATM | Mutation | Missense | ENST00000278616.4 |
g.108139268C>T
|
c.2770C>T
|
p.Arg924Trp
|
probably damaging
| B1 |
ATM | Mutation | Missense | ENST00000278616.4 |
g.108114764T>C
|
c.581T>C
|
p.Val194Ala
|
possibly damaging
| Li7 |
ATM | Mutation | Missense | ENST00000278616.4 |
g.108141831C>G
|
c.2879C>G
|
p.Pro960Arg
|
possibly damaging
| JHH2 |
ATM | Mutation | Missense | ENST00000278616.4 |
g.108138000C>G
|
c.2569C>G
|
p.Leu857Val
|
probably damaging
| JHH5 |
ATM | Mutation | Truncating | ENST00000278616.4 |
g.108143337G>C
|
c.3153+3G>C
|
p.?
|
damaging
| Huh6 |