| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229268 |
| Start |
6865223:6865223(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs782621306
|
| CDS Mutation |
c.2458G>A |
| AA Mutation |
p.Val820Ile(p.V820I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229268 |
| Start |
6864864:6864864(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2387A>T |
| AA Mutation |
p.Asp796Val(p.D796V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000229268 |
| Start |
6864120:6864120(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2169T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |