Gene >> MCM8
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000378896 |
| Start |
5993585:5993585(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2320T>C |
| AA Mutation |
p.Ser774Pro(p.S774P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000378896 |
| Start |
5955248:5955248(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.483T>A |
| AA Mutation |
p.His161Gln(p.H161Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |