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/ Colorectal Cancer-Mutation
Primary Site >> Colorectal Cancer
Overview
Mutation
Expression
Methylation
Prognosis
Literature
Timeline
Colon Cancer: Gene >> WTAP
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000358372
Start
159755342:159755342(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.922G>T
AA Mutation
p.Gly308Trp(p.G308W)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000358372
Start
159753492:159753492(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.485G>A
AA Mutation
p.Arg162Gln(p.R162Q)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant
Transcription ID
ENST00000358372
Start
159748299:159748299(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.382C>G
AA Mutation
p.Leu128Val(p.L128V)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000358372
Start
159753484:159753484(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.477G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000358372
Start
159748229:159748229(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs779533624
CDS Mutation
c.312C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000358372
Start
159755113:159755113(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.693G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
stop_gained
Transcription ID
ENST00000358372
Start
159738993:159738993(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.34C>T
AA Mutation
p.Arg12Ter(p.R12*)
Mutation Classification
Nonsense_Mutation
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
stop_gained
Transcription ID
ENST00000358372
Start
159743754:159743754(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.235C>T
AA Mutation
p.Arg79Ter(p.R79*)
Mutation Classification
Nonsense_Mutation
Feature Type
Transcript
Rectum Cancer: Gene >> WTAP
No Mutation Annotation!