| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367580 |
| Start |
181053637:181053637(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.945G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367580 |
| Start |
181052452:181052452(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.822C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
8 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000367580 |
| Start |
181052314:181052314(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.689delC |
| AA Mutation |
p.Pro230GlnfsTer5(p.P230Qfs*5) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |