| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256078 |
| Start |
25245351:25245351(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs121913530
|
| CDS Mutation |
c.34G>C |
| AA Mutation |
p.Gly12Arg(p.G12R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256078 |
| Start |
25227343:25227343(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs121913238
|
| CDS Mutation |
c.181C>A |
| AA Mutation |
p.Gln61Lys(p.Q61K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000256078 |
| Start |
25227344:25227344(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs397517037
|
| CDS Mutation |
c.180T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |