| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000597629 |
| Start |
39408687:39408688(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.988_989delGT |
| AA Mutation |
p.Val330PhefsTer2(p.V330Ffs*2) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000597629 |
| Start |
39408431:39408431(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.736delC |
| AA Mutation |
p.Leu246TrpfsTer126(p.L246Wfs*126) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> ZFP36
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000597629 |
| Start |
39408658:39408658(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.958C>G |
| AA Mutation |
p.Arg320Gly(p.R320G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000597629 |
| Start |
39408414:39408414(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.714C>A |
| AA Mutation |
p.Phe238Leu(p.F238L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|