| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265678 |
| Start |
166451229:166451229(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1080T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265678 |
| Start |
166488903:166488903(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.837G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265678 |
| Start |
166498586:166498586(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769744713
|
| CDS Mutation |
c.669C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |