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/ Colorectal Cancer-Mutation
Primary Site >> Colorectal Cancer
Overview
Mutation
Expression
Methylation
Prognosis
Literature
Timeline
Colon Cancer: Gene >> BSG
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000333511
Start
577944:577944(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.238C>T
AA Mutation
p.His80Tyr(p.H80Y)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000333511
Start
572642:572642(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.8C>T
AA Mutation
p.Ala3Val(p.A3V)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant
Transcription ID
ENST00000333511
Start
581490:581490(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.968C>T
AA Mutation
p.Ala323Val(p.A323V)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
missense_variant
Transcription ID
ENST00000333511
Start
578092:578092(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs780701101
CDS Mutation
c.386G>A
AA Mutation
p.Arg129His(p.R129H)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000333511
Start
577880:577880(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.174T>C
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000333511
Start
579609:579609(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs752283788
CDS Mutation
c.525C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000333511
Start
581473:581473(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs770815368
CDS Mutation
c.951C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
frameshift_variant
Transcription ID
ENST00000333511
Start
579603:579603(version: GRCh38)
Mutation Type
DEL
dbSNP_RS
null
CDS Mutation
c.524delG
AA Mutation
p.Gly175AlafsTer4(p.G175Afs*4)
Mutation Classification
Frame_Shift_Del
Feature Type
Transcript
Rectum Cancer: Gene >> BSG
No Mutation Annotation!