| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226284 |
| Start |
87811378:87811378(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.422A>T |
| AA Mutation |
p.Asn141Ile(p.N141I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000226284 |
| Start |
87811451:87811451(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.495C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000226284 |
| Start |
87806149:87806149(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.211G>T |
| AA Mutation |
p.Gly71Ter(p.G71*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |