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/ Colorectal Cancer-Mutation
Primary Site >> Colorectal Cancer
Overview
Mutation
Expression
Methylation
Prognosis
Literature
Timeline
Colon Cancer: Gene >> NUDT18
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000611621
Start
22107613:22107613(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs375524530
CDS Mutation
c.659G>A
AA Mutation
p.Gly220Asp(p.G220D)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000611621
Start
22107472:22107472(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.800G>A
AA Mutation
p.Gly267Asp(p.G267D)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant
Transcription ID
ENST00000611621
Start
22107663:22107663(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.609G>T
AA Mutation
p.Trp203Cys(p.W203C)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
missense_variant
Transcription ID
ENST00000611621
Start
22107344:22107344(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.928C>T
AA Mutation
p.Leu310Phe(p.L310F)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
missense_variant
Transcription ID
ENST00000611621
Start
22108339:22108339(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.170T>C
AA Mutation
p.Val57Ala(p.V57A)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000611621
Start
22108329:22108329(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.180C>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000611621
Start
22107450:22107450(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.822G>T
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
frameshift_variant
Transcription ID
ENST00000611621
Start
22108302:22108302(version: GRCh38)
Mutation Type
DEL
dbSNP_RS
novel
CDS Mutation
c.207delG
AA Mutation
p.Ser70ArgfsTer23(p.S70Rfs*23)
Mutation Classification
Frame_Shift_Del
Feature Type
Transcript
Rectum Cancer: Gene >> NUDT18
No Mutation Annotation!