Colon Cancer: Gene >> TMEM97
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226230 |
| Start |
28326749:28326749(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs782802077
|
| CDS Mutation |
c.487C>T |
| AA Mutation |
p.Arg163Trp(p.R163W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000226230 |
| Start |
28326781:28326782(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.527_528delAA |
| AA Mutation |
p.Lys176MetfsTer10(p.K176Mfs*10) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TMEM97
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226230 |
| Start |
28325642:28325642(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.266T>A |
| AA Mutation |
p.Leu89His(p.L89H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000226230 |
| Start |
28325643:28325643(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.267C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|