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/ Colorectal Cancer-Mutation
Primary Site >> Colorectal Cancer
Overview
Mutation
Expression
Methylation
Prognosis
Literature
Timeline
Colon Cancer: Gene >> BEAN1
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000536005
Start
66480893:66480893(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.748G>A
AA Mutation
p.Ala250Thr(p.A250T)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000536005
Start
66477670:66477670(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.400G>A
AA Mutation
p.Ala134Thr(p.A134T)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant
Transcription ID
ENST00000536005
Start
66480744:66480744(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.599C>T
AA Mutation
p.Pro200Leu(p.P200L)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
missense_variant
Transcription ID
ENST00000536005
Start
66480756:66480756(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.611G>A
AA Mutation
p.Gly204Asp(p.G204D)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
missense_variant
Transcription ID
ENST00000536005
Start
66480857:66480857(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.712C>A
AA Mutation
p.Pro238Thr(p.P238T)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
missense_variant
Transcription ID
ENST00000536005
Start
66477584:66477584(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.314G>A
AA Mutation
p.Arg105His(p.R105H)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000536005
Start
66477567:66477567(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.297C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
frameshift_variant
Transcription ID
ENST00000536005
Start
66477631:66477631(version: GRCh38)
Mutation Type
DEL
dbSNP_RS
novel
CDS Mutation
c.365delC
AA Mutation
p.Pro122HisfsTer50(p.P122Hfs*50)
Mutation Classification
Frame_Shift_Del
Feature Type
Transcript
Rectum Cancer: Gene >> BEAN1
No Mutation Annotation!