Gene >> LPO
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262290 |
| Start |
58267876:58267876(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2021C>T |
| AA Mutation |
p.Thr674Ile(p.T674I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262290 |
| Start |
58264904:58264904(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1449G>T |
| AA Mutation |
p.Gln483His(p.Q483H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |