Gene >> EPX
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000225371 |
| Start |
58199051:58199051(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1132T>C |
| AA Mutation |
p.Ser378Pro(p.S378P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000225371 |
| Start |
58204281:58204281(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2006T>C |
| AA Mutation |
p.Ile669Thr(p.I669T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |