Colon Cancer: Gene >> MAFB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373313 |
| Start |
40688478:40688478(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.373G>A |
| AA Mutation |
p.Asp125Asn(p.D125N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373313 |
| Start |
40688555:40688555(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.296C>T |
| AA Mutation |
p.Ala99Val(p.A99V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> MAFB
| Mutation ID |
1 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000373313 |
| Start |
40687968:40687969(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.882dupC |
| AA Mutation |
p.Lys295GlnfsTer51(p.K295Qfs*51) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
|