Primary Site >> Stomach Cancer

Gene >> CLDN12

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000287916
Start 90412918:90412918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.242T>C
AA Mutation p.Leu81Pro(p.L81P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000287916
Start 90412698:90412698(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761164855
CDS Mutation c.22G>A
AA Mutation p.Ala8Thr(p.A8T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000287916
Start 90413136:90413136(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.460G>T
AA Mutation p.Val154Phe(p.V154F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000287916
Start 90413379:90413379(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.703A>G
AA Mutation p.Ile235Val(p.I235V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000287916
Start 90413368:90413368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.692C>T
AA Mutation p.Ser231Phe(p.S231F)
Mutation Classification Missense_Mutation
Feature Type Transcript