| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000409257 |
| Start |
78202527:78202527(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.183G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000409257 |
| Start |
78187421:78187421(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs745962259
|
| CDS Mutation |
c.51G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
start_lost |
| Transcription ID |
ENST00000409257 |
| Start |
78187371:78187371(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1A>G |
| AA Mutation |
p.Met1?(p.M1?) |
| Mutation Classification |
Translation_Start_Site |
| Feature Type |
Transcript |