Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ANXA4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000394295
Start 69818625:69818625(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.655C>G
AA Mutation p.Gln219Glu(p.Q219E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000394295
Start 69818650:69818650(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.680A>C
AA Mutation p.Lys227Thr(p.K227T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000394295
Start 69804547:69804547(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376382183
CDS Mutation c.112G>A
AA Mutation p.Ala38Thr(p.A38T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000394295
Start 69820742:69820742(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.827C>T
AA Mutation p.Ser276Phe(p.S276F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence splice_donor_variant
Transcription ID ENST00000394295
Start 69810674:69810674(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.477+1G>A
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> ANXA4

No Mutation Annotation!