| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371116 |
| Start |
63324153:63324153(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1095G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371116 |
| Start |
63323226:63323226(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.168C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000371116 |
| Start |
63323334:63323334(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.281delG |
| AA Mutation |
p.Gly94AlafsTer46(p.G94Afs*46) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |