| Mutation ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256593 |
| Start |
109717372:109717372(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.603C>G |
| AA Mutation |
p.Ser201Arg(p.S201R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000256593 |
| Start |
109715130:109715130(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.457A>T |
| AA Mutation |
p.Ile153Phe(p.I153F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> GSTM5
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256593 |
| Start |
109713712:109713712(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs766842191
|
| CDS Mutation |
c.311T>C |
| AA Mutation |
p.Val104Ala(p.V104A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|