Gene >> MCM2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265056 |
| Start |
127620767:127620767(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763364817
|
| CDS Mutation |
c.2335C>T |
| AA Mutation |
p.Arg779Cys(p.R779C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265056 |
| Start |
127606649:127606649(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.933G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |