| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000204549 |
| Start |
65118749:65118749(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1426G>A |
| AA Mutation |
p.Asp476Asn(p.D476N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000204549 |
| Start |
65129117:65129117(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.924delA |
| AA Mutation |
p.Lys308AsnfsTer18(p.K308Nfs*18) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PDCD7
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000204549 |
| Start |
65119880:65119880(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768472715
|
| CDS Mutation |
c.1084C>T |
| AA Mutation |
p.Arg362Cys(p.R362C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000204549 |
| Start |
65119740:65119740(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1224G>C |
| AA Mutation |
p.Glu408Asp(p.E408D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|