| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000423485 |
| Start |
40411151:40411151(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1161C>A |
| AA Mutation |
p.Ser387Arg(p.S387R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000423485 |
| Start |
40390120:40390120(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4312C>T |
| AA Mutation |
p.Pro1438Ser(p.P1438S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000423485 |
| Start |
40406847:40406847(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1722C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |