Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CLDN12

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000287916
Start 90413232:90413232(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.556T>C
AA Mutation p.Phe186Leu(p.F186L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000287916
Start 90413227:90413227(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.551G>A
AA Mutation p.Gly184Asp(p.G184D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000287916
Start 90412924:90412924(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.248T>C
AA Mutation p.Leu83Pro(p.L83P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000287916
Start 90413157:90413157(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.481C>A
AA Mutation p.Leu161Met(p.L161M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000287916
Start 90413021:90413021(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.345C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000287916
Start 90412730:90412730(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374340236
CDS Mutation c.54C>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> CLDN12

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000287916
Start 90413278:90413278(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767199576
CDS Mutation c.602C>A
AA Mutation p.Ser201Tyr(p.S201Y)
Mutation Classification Missense_Mutation
Feature Type Transcript