| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000226279 |
| Start |
15778444:15778444(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.30C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000226279 |
| Start |
15840029:15840029(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.666delT |
| AA Mutation |
p.Phe222LeufsTer17(p.F222Lfs*17) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| ID |
8 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000226279 |
| Start |
15848580:15848580(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.881C>A |
| AA Mutation |
p.Ser294Ter(p.S294*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |