Primary Site >> Stomach Cancer

Gene >> WNT3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000225512
Start 46769844:46769844(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.527G>A
AA Mutation p.Arg176His(p.R176H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000225512
Start 46768379:46768379(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1009T>C
AA Mutation p.Cys337Arg(p.C337R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000225512
Start 46769886:46769886(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.485C>T
AA Mutation p.Ala162Val(p.A162V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000225512
Start 46768495:46768495(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.893G>A
AA Mutation p.Arg298Gln(p.R298Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000225512
Start 46768720:46768720(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754298042
CDS Mutation c.668C>T
AA Mutation p.Ala223Val(p.A223V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000225512
Start 46773820:46773820(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.170G>A
AA Mutation p.Arg57His(p.R57H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000225512
Start 46768557:46768557(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.831C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000225512
Start 46769903:46769903(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.468C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000225512
Start 46768719:46768719(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.669G>A
Mutation Classification Silent
Feature Type Transcript