Gene >> LCN2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000277480 |
| Start |
128149657:128149657(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.132C>A |
| AA Mutation |
p.Asp44Glu(p.D44E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000277480 |
| Start |
128150303:128150303(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775328996
|
| CDS Mutation |
c.204G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |