| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000527636 |
| Start |
12764244:12764244(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.12C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000527636 |
| Start |
12879839:12879839(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.465+1delG |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000527636 |
| Start |
12924949:12924950(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.916dupT |
| AA Mutation |
p.Tyr306LeufsTer11(p.Y306Lfs*11) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |