Gene >> EGR3
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317216 |
| Start |
22691093:22691093(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.544G>T |
| AA Mutation |
p.Ala182Ser(p.A182S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000317216 |
| Start |
22690767:22690767(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.870C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |