Gene >> SP1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000327443 |
| Start |
53383331:53383331(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1384G>A |
| AA Mutation |
p.Val462Ile(p.V462I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000327443 |
| Start |
53406688:53406688(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1779C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |