| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000312648 |
| Start |
82316757:82316757(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs149247674
|
| CDS Mutation |
c.307C>T |
| AA Mutation |
p.Arg103Cys(p.R103C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000312648 |
| Start |
82315367:82315367(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs751672673
|
| CDS Mutation |
c.677C>T |
| AA Mutation |
p.Ser226Leu(p.S226L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CD7
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000312648 |
| Start |
82316842:82316842(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.222C>A |
| AA Mutation |
p.Asp74Glu(p.D74E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|