| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000343380 |
| Start |
33677291:33677291(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762296081
|
| CDS Mutation |
c.880G>A |
| AA Mutation |
p.Asp294Asn(p.D294N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000343380 |
| Start |
33677529:33677529(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.737T>C |
| AA Mutation |
p.Val246Ala(p.V246A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000343380 |
| Start |
33677157:33677157(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1014C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |