| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000337138 |
| Start |
61720523:61720523(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.177G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000337138 |
| Start |
61721783:61721783(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.417T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
8 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000337138 |
| Start |
61740629:61740629(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1659+2T>C |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |