| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000366553 |
| Start |
241634482:241634482(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs753456268
|
| CDS Mutation |
c.1285A>G |
| AA Mutation |
p.Ile429Val(p.I429V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000366553 |
| Start |
241635091:241635091(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.676G>A |
| AA Mutation |
p.Gly226Ser(p.G226S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000366553 |
| Start |
241635746:241635746(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs369552093
|
| CDS Mutation |
c.21A>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |