Gene >> CALCR
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000359558 |
| Start |
93426570:93426570(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1313G>A |
| AA Mutation |
p.Arg438His(p.R438H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000359558 |
| Start |
93443714:93443714(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.794C>T |
| AA Mutation |
p.Ala265Val(p.A265V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |