Gene >> REM1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000201979 |
| Start |
31476533:31476533(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.88C>A |
| AA Mutation |
p.Pro30Thr(p.P30T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000201979 |
| Start |
31476547:31476547(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.102C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |