| Mutation ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000395473 |
| Start |
27640657:27640657(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.217G>A |
| AA Mutation |
p.Val73Met(p.V73M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000395473 |
| Start |
27648946:27648946(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1037delG |
| AA Mutation |
p.Gly346AlafsTer5(p.G346Afs*5) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> LGALS9
| Mutation ID |
1 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000395473 |
| Start |
27640725:27640725(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.288delG |
| AA Mutation |
p.Met97CysfsTer16(p.M97Cfs*16) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
|