Gene >> FOXN4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299162 |
| Start |
109281710:109281710(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.991G>A |
| AA Mutation |
p.Ala331Thr(p.A331T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299162 |
| Start |
109281538:109281538(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778183505
|
| CDS Mutation |
c.1163C>T |
| AA Mutation |
p.Pro388Leu(p.P388L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |