Gene >> MYCN
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000281043 |
| Start |
15945607:15945607(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs140581169
|
| CDS Mutation |
c.905G>A |
| AA Mutation |
p.Arg302His(p.R302H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000281043 |
| Start |
15945833:15945833(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs753698437
|
| CDS Mutation |
c.1131G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |