| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261233 |
| Start |
66245175:66245175(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1227C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000261233 |
| Start |
66211466:66211467(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.457_458delAT |
| AA Mutation |
p.Ile153GlnfsTer10(p.I153Qfs*10) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000261233 |
| Start |
66217236:66217236(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.653+1G>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |