IGFN1 | Mutation | Missense | ENST00000335211.4 |
g.201163380G>A
|
c.106G>A
|
p.Val36Ile
|
benign
| Hep3B |
IGFN1 | Mutation | Missense | ENST00000335211.4 |
g.201178199G>C
|
c.4178G>C
|
p.Arg1393Thr
|
unknown
| B1 |
IGFN1 | Mutation | Missense | ENST00000335211.4 |
g.201196334T>C
|
c.11111T>C
|
p.Ile3704Thr (Splice)
|
benign
| SNU398 |
IGFN1 | Mutation | Missense | ENST00000335211.4 |
g.201181729G>T
|
c.7708G>T
|
p.Gly2570Trp
|
damaging
| SNU475 |
IGFN1 | Mutation | Missense | ENST00000335211.4 |
g.201176558G>A
|
c.2537G>A
|
p.Ser846Asn
|
benign
| Mahlavu |
IGFN1 | Mutation | Missense | ENST00000335211.4 |
g.201176306G>T
|
c.2285G>T
|
p.Gly762Val
|
damaging
| PLC.PRF5 |
IGFN1 | Mutation | Missense | ENST00000335211.4 |
g.201186421C>T
|
c.9602C>T
|
p.Pro3201Leu
|
probably damaging
| SNU739 |
IGFN1 | Mutation | Truncating | ENST00000335211.4 |
g.201177856G>T
|
c.3835G>T
|
p.Glu1279X
|
damaging
| SNU886 |