| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000259938 |
| Start |
35795241:35795241(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs755023217
|
| CDS Mutation |
c.244C>T |
| AA Mutation |
p.Arg82Cys(p.R82C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000259938 |
| Start |
35797258:35797258(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs529464575
|
| CDS Mutation |
c.31G>A |
| AA Mutation |
p.Ala11Thr(p.A11T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000259938 |
| Start |
35795159:35795159(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs780396671
|
| CDS Mutation |
c.326G>A |
| AA Mutation |
p.Arg109His(p.R109H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |