Gene >> KLHL2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226725 |
| Start |
165299538:165299538(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs751575614
|
| CDS Mutation |
c.803G>A |
| AA Mutation |
p.Ser268Asn(p.S268N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000226725 |
| Start |
165228819:165228819(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.165G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |