Primary Site >> Stomach Cancer

Gene >> WNT6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000233948
Start 218871590:218871590(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.407C>T
AA Mutation p.Ala136Val(p.A136V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000233948
Start 218871512:218871512(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.329C>T
AA Mutation p.Ala110Val(p.A110V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000233948
Start 218873666:218873666(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.919G>A
AA Mutation p.Gly307Ser(p.G307S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000233948
Start 218871704:218871704(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.521A>G
AA Mutation p.Asp174Gly(p.D174G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000233948
Start 218873663:218873663(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.916C>T
AA Mutation p.Arg306Cys(p.R306C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000233948
Start 218871680:218871680(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.497C>T
AA Mutation p.Ala166Val(p.A166V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000233948
Start 218871507:218871507(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.324G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000233948
Start 218871780:218871780(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.597C>T
Mutation Classification Silent
Feature Type Transcript