| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264335 |
| Start |
1361260:1361260(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.410C>T |
| AA Mutation |
p.Thr137Ile(p.T137I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264335 |
| Start |
1364865:1364865(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.258G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000264335 |
| Start |
1354264:1354266(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.660_662delCAT |
| AA Mutation |
p.Ile220del(p.I220del) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |