| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000220763 |
| Start |
97066140:97066140(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1185C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000220763 |
| Start |
96785149:96785149(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.252A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000220763 |
| Start |
96879868:96879878(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.716_726delCAGAAATGATG |
| AA Mutation |
p.Ala239ValfsTer25(p.A239Vfs*25) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |