Gene >> EGR1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000239938 |
| Start |
138467007:138467007(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.558G>T |
| AA Mutation |
p.Gln186His(p.Q186H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000239938 |
| Start |
138468064:138468064(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1615A>G |
| AA Mutation |
p.Thr539Ala(p.T539A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |