| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376694 |
| Start |
30172214:30172214(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1263C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376694 |
| Start |
30163966:30163966(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs143039782
|
| CDS Mutation |
c.282C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000376694 |
| Start |
30163881:30163882(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.201_202dupGA |
| AA Mutation |
p.Thr68ArgfsTer71(p.T68Rfs*71) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |