| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000317775 |
| Start |
117280797:117280797(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1452C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000317775 |
| Start |
117234677:117234677(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3123C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
8 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000317775 |
| Start |
117265391:117265391(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2061delC |
| AA Mutation |
p.Met688CysfsTer52(p.M688Cfs*52) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |