| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296870 |
| Start |
132060722:132060722(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370114748
|
| CDS Mutation |
c.16G>A |
| AA Mutation |
p.Val6Ile(p.V6I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296870 |
| Start |
132062766:132062766(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs780057953
|
| CDS Mutation |
c.434C>T |
| AA Mutation |
p.Thr145Met(p.T145M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000296870 |
| Start |
132062725:132062725(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750120195
|
| CDS Mutation |
c.393G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |