Gene >> NR1I3
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367982 |
| Start |
161235959:161235959(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.126C>G |
| AA Mutation |
p.Ser42Arg(p.S42R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367982 |
| Start |
161231141:161231141(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.799G>C |
| AA Mutation |
p.Ala267Pro(p.A267P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |