Gene >> BNC1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000345382 |
| Start |
83257668:83257668(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2759C>T |
| AA Mutation |
p.Ala920Val(p.A920V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000345382 |
| Start |
83257922:83257922(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2505G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |