| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303714 |
| Start |
69077428:69077428(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.582T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303714 |
| Start |
69181857:69181857(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762651259
|
| CDS Mutation |
c.1161C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303714 |
| Start |
69152204:69152204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs749173652
|
| CDS Mutation |
c.987C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |