| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000337714 |
| Start |
57110045:57110045(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1735G>T |
| AA Mutation |
p.Asp579Tyr(p.D579Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000337714 |
| Start |
57106369:57106369(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.905G>A |
| AA Mutation |
p.Gly302Glu(p.G302E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000337714 |
| Start |
57105524:57105524(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.60C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |