| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361566 |
| Start |
41523803:41523803(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1143C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000361566 |
| Start |
41528068:41528068(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.180delC |
| AA Mutation |
p.Tyr61ThrfsTer9(p.Y61Tfs*9) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| ID |
8 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000361566 |
| Start |
41523818:41523820(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1126_1128delGAG |
| AA Mutation |
p.Glu376del(p.E376del) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |