| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000234111 |
| Start |
10442151:10442151(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs114981547
|
| CDS Mutation |
c.774G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000234111 |
| Start |
10441844:10441844(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs530654829
|
| CDS Mutation |
c.999C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000234111 |
| Start |
10440829:10440829(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370233699
|
| CDS Mutation |
c.1281C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |