Gene >> RBM4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310092 |
| Start |
66639760:66639760(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.49G>C |
| AA Mutation |
p.Glu17Gln(p.E17Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310092 |
| Start |
66643630:66643630(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs577949918
|
| CDS Mutation |
c.593G>A |
| AA Mutation |
p.Arg198His(p.R198H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |