| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369230 |
| Start |
116466156:116466156(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.915A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369230 |
| Start |
116443129:116443129(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.279A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000369230 |
| Start |
116443175:116443175(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767204004
|
| CDS Mutation |
c.324+1G>C |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |