| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000270218 |
| Start |
206841021:206841021(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.381T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000270218 |
| Start |
206836731:206836731(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs374799009
|
| CDS Mutation |
c.69C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000270218 |
| Start |
206836807:206836807(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776351317
|
| CDS Mutation |
c.144+1G>A |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |