Gene >> CLSTN1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377298 |
| Start |
9743912:9743912(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1328C>T |
| AA Mutation |
p.Pro443Leu(p.P443L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000377298 |
| Start |
9730571:9730571(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs746014551
|
| CDS Mutation |
c.2883C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |