Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HJURP

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000411486
Start 233842180:233842180(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.600G>C
AA Mutation p.Lys200Asn(p.K200N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000411486
Start 233841804:233841804(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.976C>T
AA Mutation p.Pro326Ser(p.P326S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000411486
Start 233841129:233841129(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1651A>G
AA Mutation p.Ile551Val(p.I551V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000411486
Start 233840703:233840703(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771833145
CDS Mutation c.2077C>T
AA Mutation p.Arg693Cys(p.R693C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000411486
Start 233842073:233842073(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.707T>G
AA Mutation p.Leu236Arg(p.L236R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000411486
Start 233841702:233841702(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1078C>A
AA Mutation p.Leu360Ile(p.L360I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000411486
Start 233841151:233841151(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs76212469
CDS Mutation c.1629C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000411486
Start 233840701:233840701(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2079C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000411486
Start 233841610:233841610(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749524750
CDS Mutation c.1170C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000411486
Start 233840931:233840931(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765753648
CDS Mutation c.1849C>T
AA Mutation p.Arg617Ter(p.R617*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> HJURP

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000411486
Start 233840996:233840996(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1784C>A
AA Mutation p.Ser595Tyr(p.S595Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000411486
Start 233841702:233841702(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1078C>A
AA Mutation p.Leu360Ile(p.L360I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000411486
Start 233841131:233841131(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1649G>A
AA Mutation p.Gly550Glu(p.G550E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000411486
Start 233841085:233841085(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1695A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000411486
Start 233841817:233841817(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.963G>A
Mutation Classification Silent
Feature Type Transcript