| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000392213 |
| Start |
35309956:35309956(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1314G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000392213 |
| Start |
35299828:35299828(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.690C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000392213 |
| Start |
35310007:35310016(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1368_1377delCGAGCGGGAG |
| AA Mutation |
p.Glu457SerfsTer50(p.E457Sfs*50) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |