| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000382496 |
| Start |
9197261:9197261(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs765586378
|
| CDS Mutation |
c.975C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000382496 |
| Start |
9379920:9379920(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.27G>A |
| AA Mutation |
p.Trp9Ter(p.W9*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000382496 |
| Start |
9066532:9066532(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2188C>T |
| AA Mutation |
p.Arg730Ter(p.R730*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |