Gene >> ALX4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000329255 |
| Start |
44264949:44264949(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768153687
|
| CDS Mutation |
c.1141G>C |
| AA Mutation |
p.Glu381Gln(p.E381Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000329255 |
| Start |
44275404:44275404(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750798110
|
| CDS Mutation |
c.721G>A |
| AA Mutation |
p.Val241Met(p.V241M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |