LGR6 | Mutation | Missense | ENST00000367278.3 |
g.202287956G>A
|
c.2525G>A
|
p.Arg842Gln
|
possibly damaging
| HLE |
LGR6 | Mutation | Missense | ENST00000367278.3 |
g.202287956G>A
|
c.2525G>A
|
p.Arg842Gln
|
possibly damaging
| HLF |
LGR6 | Mutation | Missense | ENST00000367278.3 |
g.202266680G>A
|
c.761G>A
|
p.Arg254Gln
|
possibly damaging
| Li7 |
LGR6 | Mutation | Missense | ENST00000367278.3 |
g.202287634G>A
|
c.2203G>A
|
p.Ala735Thr
|
possibly damaging
| JHH1 |
LGR6 | Mutation | Missense | ENST00000439764.2 |
g.202183337G>T
|
c.55G>T
|
p.Ala19Ser
|
benign
| SNU761 |