| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262101 |
| Start |
16168825:16168825(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.263C>T |
| AA Mutation |
p.Thr88Ile(p.T88I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262101 |
| Start |
16168584:16168584(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776045116
|
| CDS Mutation |
c.504A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262101 |
| Start |
16110121:16110121(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1320A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |