Gene >> IFNL2
| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000331982 |
| Start |
39269523:39269523(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.306G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000331982 |
| Start |
39268834:39268834(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.168C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |