Gene >> MYCN
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000281043 |
| Start |
15945897:15945897(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1195T>A |
| AA Mutation |
p.Ser399Thr(p.S399T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000281043 |
| Start |
15945606:15945606(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs144939456
|
| CDS Mutation |
c.904C>T |
| AA Mutation |
p.Arg302Cys(p.R302C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |