| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375749 |
| Start |
32234584:32234584(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1090C>T |
| AA Mutation |
p.Arg364Trp(p.R364W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
inframe_deletion |
| Transcription ID |
ENST00000375749 |
| Start |
32216706:32216708(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.529_531delCAA |
| AA Mutation |
p.Gln177del(p.Q177del) |
| Mutation Classification |
In_Frame_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> POFUT1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375749 |
| Start |
32228340:32228340(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.620C>T |
| AA Mutation |
p.Pro207Leu(p.P207L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|