Gene >> RCAN2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330430 |
| Start |
46248865:46248865(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.119A>G |
| AA Mutation |
p.Asp40Gly(p.D40G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330430 |
| Start |
46223239:46223239(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs556179069
|
| CDS Mutation |
c.496G>A |
| AA Mutation |
p.Asp166Asn(p.D166N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |