| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000482890 |
| Start |
10404612:10404612(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.660C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000482890 |
| Start |
10406804:10406805(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.520_521delGT |
| AA Mutation |
p.Val174AsnfsTer2(p.V174Nfs*2) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000482890 |
| Start |
10402495:10402495(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.880G>T |
| AA Mutation |
p.Glu294Ter(p.E294*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |