| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000271640 |
| Start |
150942988:150942988(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.810T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000271640 |
| Start |
150927801:150927801(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.87G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000271640 |
| Start |
150960947:150960947(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2885C>G |
| AA Mutation |
p.Ser962Ter(p.S962*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |