Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EZR

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000337147
Start 158785535:158785535(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369743003
CDS Mutation c.241C>T
AA Mutation p.Arg81Trp(p.R81W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000337147
Start 158785396:158785396(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.380C>T
AA Mutation p.Ser127Phe(p.S127F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000337147
Start 158787121:158787121(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.179A>T
AA Mutation p.Lys60Met(p.K60M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000337147
Start 158767418:158767418(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1439C>A
AA Mutation p.Pro480Gln(p.P480Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000337147
Start 158769872:158769872(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs571220845
CDS Mutation c.1163G>A
AA Mutation p.Arg388His(p.R388H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000337147
Start 158767075:158767075(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1600C>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> EZR

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000337147
Start 158769815:158769815(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1220C>T
AA Mutation p.Ala407Val(p.A407V)
Mutation Classification Missense_Mutation
Feature Type Transcript