Gene >> CERS2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000271688 |
| Start |
150966161:150966161(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs779228104
|
| CDS Mutation |
c.1130G>A |
| AA Mutation |
p.Arg377His(p.R377H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000271688 |
| Start |
150968442:150968442(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.244G>A |
| AA Mutation |
p.Ala82Thr(p.A82T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |