| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000451237 |
| Start |
33278372:33278372(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.953C>T |
| AA Mutation |
p.Pro318Leu(p.P318L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000451237 |
| Start |
33278139:33278139(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.725delG |
| AA Mutation |
p.Gly242AlafsTer48(p.G242Afs*48) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> B3GALT4
| Mutation ID |
1 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000451237 |
| Start |
33278138:33278139(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
rs779828300
|
| CDS Mutation |
c.725dupG |
| AA Mutation |
p.Arg243GlnfsTer108(p.R243Qfs*108) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
|