| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336458 |
| Start |
7311417:7311417(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.338G>A |
| AA Mutation |
p.Arg113His(p.R113H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336458 |
| Start |
7311630:7311630(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.455T>C |
| AA Mutation |
p.Met152Thr(p.M152T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000336458 |
| Start |
7311355:7311355(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.276T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |