Gene >> FOXL2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330315 |
| Start |
138946089:138946089(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750300712
|
| CDS Mutation |
c.634C>G |
| AA Mutation |
p.Pro212Ala(p.P212A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330315 |
| Start |
138946068:138946068(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.655C>G |
| AA Mutation |
p.Gln219Glu(p.Q219E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |