Colon Cancer: Gene >> LIN28B
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000345080 |
| Start |
105078680:105078680(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs76912525
|
| CDS Mutation |
c.650G>A |
| AA Mutation |
p.Arg217Gln(p.R217Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> LIN28B
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000345080 |
| Start |
105078754:105078754(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.724C>T |
| AA Mutation |
p.Pro242Ser(p.P242S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000345080 |
| Start |
105026408:105026409(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.312dupG |
| AA Mutation |
p.Ser105GlufsTer7(p.S105Efs*7) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
|