Gene >> RGN
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336169 |
| Start |
47089823:47089823(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.394G>T |
| AA Mutation |
p.Gly132Trp(p.G132W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336169 |
| Start |
47081277:47081277(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.133T>A |
| AA Mutation |
p.Phe45Ile(p.F45I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |