| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000442267 |
| Start |
140659663:140659663(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1846G>A |
| AA Mutation |
p.Glu616Lys(p.E616K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000442267 |
| Start |
140662053:140662053(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1643A>T |
| AA Mutation |
p.Lys548Met(p.K548M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000442267 |
| Start |
140669637:140669637(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1434A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |