| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000324602 |
| Start |
54631571:54631571(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.142A>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000324602 |
| Start |
54636529:54636529(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752672185
|
| CDS Mutation |
c.1689G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000324602 |
| Start |
54631616:54631617(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.191dupA |
| AA Mutation |
p.Lys65GlufsTer38(p.K65Efs*38) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |