| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000571995 |
| Start |
82658062:82658062(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.638C>T |
| AA Mutation |
p.Pro213Leu(p.P213L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000571995 |
| Start |
82657910:82657910(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
rs750486067
|
| CDS Mutation |
c.790delC |
| AA Mutation |
p.Gln264ArgfsTer88(p.Q264Rfs*88) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RAB40B
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000571995 |
| Start |
82657872:82657872(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.828A>C |
| AA Mutation |
p.Lys276Asn(p.K276N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|