| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262461 |
| Start |
128151334:128151334(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2201C>G |
| AA Mutation |
p.Ala734Gly(p.A734G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262461 |
| Start |
128152769:128152769(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs373411636
|
| CDS Mutation |
c.2327G>A |
| AA Mutation |
p.Arg776His(p.R776H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262461 |
| Start |
128161710:128161710(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2526T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |