Gene >> BBC3
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000449228 |
| Start |
47221904:47221904(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs751834949
|
| CDS Mutation |
c.583G>A |
| AA Mutation |
p.Ala195Thr(p.A195T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000449228 |
| Start |
47221752:47221752(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.735C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |