| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368033 |
| Start |
160841410:160841410(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.470G>A |
| AA Mutation |
p.Cys157Tyr(p.C157Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368033 |
| Start |
160841392:160841392(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs771548413
|
| CDS Mutation |
c.488G>A |
| AA Mutation |
p.Gly163Asp(p.G163D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368033 |
| Start |
160841439:160841439(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.441C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |