| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000278968 |
| Start |
117203124:117203124(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs140777664
|
| CDS Mutation |
c.111G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000278968 |
| Start |
117203082:117203082(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.69C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
start_lost |
| Transcription ID |
ENST00000278968 |
| Start |
117203015:117203015(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2T>C |
| AA Mutation |
p.Met1?(p.M1?) |
| Mutation Classification |
Translation_Start_Site |
| Feature Type |
Transcript |