| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000322611 |
| Start |
17275468:17275468(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.252G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000322611 |
| Start |
17275414:17275414(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.198C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000322611 |
| Start |
17275293:17275294(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.80_87dupAGGGCGCG |
| AA Mutation |
p.Ala30ArgfsTer197(p.A30Rfs*197) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |