| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000301887 |
| Start |
64989783:64989783(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs754654435
|
| CDS Mutation |
c.171C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000301887 |
| Start |
64989729:64989729(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.225G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000301887 |
| Start |
64996898:64996898(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.17delG |
| AA Mutation |
p.Gly6AlafsTer5(p.G6Afs*5) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |