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/ Colorectal Cancer-Mutation
Primary Site >> Colorectal Cancer
Overview
Mutation
Expression
Methylation
Prognosis
Literature
Timeline
Colon Cancer: Gene >> RNH1
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000354420
Start
498026:498026(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs746696140
CDS Mutation
c.1072G>A
AA Mutation
p.Val358Met(p.V358M)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000354420
Start
498878:498878(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.670G>A
AA Mutation
p.Ala224Thr(p.A224T)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant
Transcription ID
ENST00000354420
Start
499857:499857(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.415G>T
AA Mutation
p.Asp139Tyr(p.D139Y)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
missense_variant
Transcription ID
ENST00000354420
Start
499102:499102(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs762505688
CDS Mutation
c.527C>T
AA Mutation
p.Thr176Met(p.T176M)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
missense_variant
Transcription ID
ENST00000354420
Start
500566:500566(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs200324639
CDS Mutation
c.190C>T
AA Mutation
p.Arg64Cys(p.R64C)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000354420
Start
499028:499028(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.601C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000354420
Start
494900:494900(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.1281C>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
frameshift_variant
Transcription ID
ENST00000354420
Start
500507:500507(version: GRCh38)
Mutation Type
DEL
dbSNP_RS
null
CDS Mutation
c.249delC
AA Mutation
p.Ser84ProfsTer7(p.S84Pfs*7)
Mutation Classification
Frame_Shift_Del
Feature Type
Transcript
Rectum Cancer: Gene >> RNH1
No Mutation Annotation!