| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265028 |
| Start |
186582001:186582001(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.606G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265028 |
| Start |
186572245:186572245(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.219T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000265028 |
| Start |
186575928:186575928(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.319delT |
| AA Mutation |
p.Ser107HisfsTer30(p.S107Hfs*30) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |