Gene >> FFAR2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000246549 |
| Start |
35450072:35450072(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.358T>G |
| AA Mutation |
p.Ser120Ala(p.S120A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000246549 |
| Start |
35449955:35449955(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.241G>T |
| AA Mutation |
p.Val81Phe(p.V81F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |