Gene >> FGF22
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000215530 |
| Start |
643536:643536(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.445C>G |
| AA Mutation |
p.Pro149Ala(p.P149A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000215530 |
| Start |
643528:643528(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
rs760964028
|
| CDS Mutation |
c.444delG |
| AA Mutation |
p.Arg150GlyfsTer?(p.R150Gfs*?) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |