| Mutation ID |
5 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000262051 |
| Start |
50999216:50999216(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.633delT |
| AA Mutation |
p.Phe211LeufsTer19(p.F211Lfs*19) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000262051 |
| Start |
50995751:50995751(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.868C>T |
| AA Mutation |
p.Arg290Ter(p.R290*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SLC11A2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262051 |
| Start |
51004801:51004801(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368158015
|
| CDS Mutation |
c.416G>A |
| AA Mutation |
p.Arg139His(p.R139H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|