Gene >> SAMHD1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262878 |
| Start |
36911265:36911265(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1223G>C |
| AA Mutation |
p.Arg408Pro(p.R408P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262878 |
| Start |
36905476:36905476(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1298C>G |
| AA Mutation |
p.Ser433Cys(p.S433C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |