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Mutation
Expression
Methylation
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Timeline
Colon Cancer: Gene >> ZBTB4
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000311403
Start
7463589:7463589(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.1393C>T
AA Mutation
p.Pro465Ser(p.P465S)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000311403
Start
7466261:7466261(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.541G>A
AA Mutation
p.Gly181Arg(p.G181R)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant
Transcription ID
ENST00000311403
Start
7462928:7462928(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.2054G>T
AA Mutation
p.Gly685Val(p.G685V)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
missense_variant
Transcription ID
ENST00000311403
Start
7462962:7462962(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs17854295
CDS Mutation
c.2020C>T
AA Mutation
p.Arg674Cys(p.R674C)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
missense_variant
Transcription ID
ENST00000311403
Start
7465883:7465883(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs775889094
CDS Mutation
c.919G>A
AA Mutation
p.Val307Met(p.V307M)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
missense_variant
Transcription ID
ENST00000311403
Start
7463762:7463762(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.1220C>A
AA Mutation
p.Pro407His(p.P407H)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
missense_variant
Transcription ID
ENST00000311403
Start
7462155:7462155(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs754134000
CDS Mutation
c.2827G>A
AA Mutation
p.Ala943Thr(p.A943T)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
missense_variant
Transcription ID
ENST00000311403
Start
7463068:7463068(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.1914G>T
AA Mutation
p.Glu638Asp(p.E638D)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
9
Mutation Consequence
missense_variant
Transcription ID
ENST00000311403
Start
7463828:7463828(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.1154G>A
AA Mutation
p.Arg385Gln(p.R385Q)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
10
Mutation Consequence
missense_variant
Transcription ID
ENST00000311403
Start
7466282:7466282(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.520C>T
AA Mutation
p.Arg174Cys(p.R174C)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
11
Mutation Consequence
missense_variant
Transcription ID
ENST00000311403
Start
7463720:7463720(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs747744082
CDS Mutation
c.1262G>A
AA Mutation
p.Arg421Gln(p.R421Q)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
12
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000311403
Start
7463677:7463677(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.1305G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
13
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000311403
Start
7466772:7466772(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs753337722
CDS Mutation
c.30G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
14
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000311403
Start
7466508:7466508(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.294C>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
15
Mutation Consequence
frameshift_variant
Transcription ID
ENST00000311403
Start
7462925:7462925(version: GRCh38)
Mutation Type
DEL
dbSNP_RS
null
CDS Mutation
c.2057delG
AA Mutation
p.Gly686AlafsTer53(p.G686Afs*53)
Mutation Classification
Frame_Shift_Del
Feature Type
Transcript
Rectum Cancer: Gene >> ZBTB4
No Mutation Annotation!