Primary Site >> Stomach Cancer

Gene >> FRZB

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295113
Start 182866174:182866174(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.379C>T
AA Mutation p.Arg127Cys(p.R127C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295113
Start 182866170:182866170(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.383A>G
AA Mutation p.His128Arg(p.H128R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295113
Start 182866213:182866213(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755911189
CDS Mutation c.340C>T
AA Mutation p.Arg114Trp(p.R114W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000295113
Start 182866274:182866274(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.279G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000295113
Start 182866127:182866127(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.426C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000295113
Start 182866217:182866217(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.336C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000295113
Start 182866301:182866301(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.252G>A
Mutation Classification Silent
Feature Type Transcript