FAM151A | Mutation | Missense | ENST00000302250.2 |
g.55078184T>G
|
c.775A>C
|
p.Ser259Arg
|
probably damaging
| HLE |
FAM151A | Mutation | Missense | ENST00000302250.2 |
g.55078184T>G
|
c.775A>C
|
p.Ser259Arg
|
probably damaging
| HLF |
FAM151A | Mutation | Missense | ENST00000302250.2 |
g.55078199C>A
|
c.760G>T
|
p.Ala254Ser
|
benign
| Huh1 |
FAM151A | Mutation | Missense | ENST00000302250.2 |
g.55078333C>G
|
c.626G>C
|
p.Gly209Ala
|
probably damaging
| JHH7 |
FAM151A | Mutation | Missense | ENST00000302250.2 |
g.55078334C>A
|
c.625G>T
|
p.Gly209Cys
|
probably damaging
| JHH7 |
FAM151A | Mutation | Missense | ENST00000302250.2 |
g.55078186A>G
|
c.773T>C
|
p.Phe258Ser
|
benign
| SNU761 |