Gene >> FGF21
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222157 |
| Start |
48756390:48756390(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.154G>A |
| AA Mutation |
p.Asp52Asn(p.D52N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000222157 |
| Start |
48758046:48758046(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.456A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |