| Mutation ID |
5 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000323963 |
| Start |
186786269:186786270(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.623_624insACTGTCATTTCTAGATCTAC |
| AA Mutation |
p.Gln209LeufsTer23(p.Q209Lfs*23) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000323963 |
| Start |
186785996:186785998(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
rs767682413
|
| CDS Mutation |
c.463_465delATT |
| AA Mutation |
p.Ile155del(p.I155del) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> EIF4A2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000323963 |
| Start |
186789141:186789141(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1096C>G |
| AA Mutation |
p.Arg366Gly(p.R366G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|