| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309988 |
| Start |
95048101:95048101(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.236G>T |
| AA Mutation |
p.Gly79Val(p.G79V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309988 |
| Start |
95048059:95048059(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.194C>G |
| AA Mutation |
p.Ala65Gly(p.A65G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000309988 |
| Start |
95049703:95049703(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs149416032
|
| CDS Mutation |
c.384C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |