| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000394820 |
| Start |
102593546:102593546(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1185G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000394820 |
| Start |
102612525:102612525(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs568273802
|
| CDS Mutation |
c.2508G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000394820 |
| Start |
102529915:102529915(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.118+1G>C |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |