Gene >> SEPT9
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000427177 |
| Start |
77482198:77482198(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.776C>T |
| AA Mutation |
p.Ala259Val(p.A259V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000427177 |
| Start |
77402163:77402163(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.181C>T |
| AA Mutation |
p.Gln61Ter(p.Q61*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |