Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> UHMK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000489294
Start 162512513:162512513(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.862G>A
AA Mutation p.Asp288Asn(p.D288N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000489294
Start 162498020:162498020(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.20C>T
AA Mutation p.Ala7Val(p.A7V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000489294
Start 162500005:162500005(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777113900
CDS Mutation c.319C>T
AA Mutation p.Arg107Cys(p.R107C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000489294
Start 162522504:162522504(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1214C>T
AA Mutation p.Pro405Leu(p.P405L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000489294
Start 162500157:162500157(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767610803
CDS Mutation c.471G>A
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> UHMK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000489294
Start 162499988:162499988(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.302C>A
AA Mutation p.Ser101Tyr(p.S101Y)
Mutation Classification Missense_Mutation
Feature Type Transcript