| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000240100 |
| Start |
29338391:29338391(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750209222
|
| CDS Mutation |
c.690G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000240100 |
| Start |
29337134:29337134(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1077C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000240100 |
| Start |
29337341:29337342(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.868_869dupAT |
| AA Mutation |
p.Cys291SerfsTer6(p.C291Sfs*6) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |