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/ Colorectal Cancer-Mutation
Primary Site >> Colorectal Cancer
Overview
Mutation
Expression
Methylation
Prognosis
Literature
Timeline
Colon Cancer: Gene >> OSBP2
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000332585
Start
30887582:30887582(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.1264G>A
AA Mutation
p.Gly422Ser(p.G422S)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000332585
Start
30870641:30870641(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs773995691
CDS Mutation
c.1066C>T
AA Mutation
p.Arg356Trp(p.R356W)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant
Transcription ID
ENST00000332585
Start
30741351:30741351(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs753497112
CDS Mutation
c.835G>A
AA Mutation
p.Val279Met(p.V279M)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000332585
Start
30695047:30695047(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.138C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000332585
Start
30905984:30905984(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.2523G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000332585
Start
30741332:30741332(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.816C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000332585
Start
30870556:30870556(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs34660027
CDS Mutation
c.981C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000332585
Start
30905843:30905843(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.2382C>T
Mutation Classification
Silent
Feature Type
Transcript
Rectum Cancer: Gene >> OSBP2
No Mutation Annotation!