| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000221476 |
| Start |
45311876:45311876(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.526C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000221476 |
| Start |
45306909:45306909(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.987C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000221476 |
| Start |
45307528:45307528(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs538248814
|
| CDS Mutation |
c.900G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |