| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000244217 |
| Start |
71124378:71124378(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.206T>C |
| AA Mutation |
p.Leu69Pro(p.L69P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000244217 |
| Start |
71124377:71124377(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.207G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> MCEE
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000244217 |
| Start |
71124444:71124444(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs377624743
|
| CDS Mutation |
c.140G>A |
| AA Mutation |
p.Arg47Gln(p.R47Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000244217 |
| Start |
71124462:71124462(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.122C>A |
| AA Mutation |
p.Ser41Tyr(p.S41Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|