| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358273 |
| Start |
31261795:31261795(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4662G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000358273 |
| Start |
31337876:31337876(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.6700C>T |
| AA Mutation |
p.Gln2234Ter(p.Q2234*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000358273 |
| Start |
31235963:31235963(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3916C>T |
| AA Mutation |
p.Arg1306Ter(p.R1306*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |