Primary Site >> Colorectal Cancer

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!