| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367851 |
| Start |
167823027:167823027(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4149G>T |
| AA Mutation |
p.Leu1383Phe(p.L1383F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367851 |
| Start |
167845806:167845806(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs772519958
|
| CDS Mutation |
c.2764G>A |
| AA Mutation |
p.Glu922Lys(p.E922K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367851 |
| Start |
167875159:167875159(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1434C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |