Primary Site >> Stomach Cancer

Gene >> WNT11

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000322563
Start 76187168:76187168(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.962A>G
AA Mutation p.Tyr321Cys(p.Y321C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000322563
Start 76196623:76196623(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201232636
CDS Mutation c.179G>A
AA Mutation p.Arg60His(p.R60H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000322563
Start 76194784:76194784(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.380C>T
AA Mutation p.Ala127Val(p.A127V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000322563
Start 76191848:76191848(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371219834
CDS Mutation c.606C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000322563
Start 76187089:76187089(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779203205
CDS Mutation c.1041C>T
Mutation Classification Silent
Feature Type Transcript