Primary Site >> Stomach Cancer

Gene >> RTCA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370128
Start 100275687:100275687(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.704C>T
AA Mutation p.Pro235Leu(p.P235L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370128
Start 100285303:100285303(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.875A>G
AA Mutation p.Asp292Gly(p.D292G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370128
Start 100274906:100274906(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.556C>T
AA Mutation p.Arg186Cys(p.R186C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000370128
Start 100291441:100291441(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs533716553
CDS Mutation c.1038C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000370128
Start 100268204:100268204(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.199C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000370128
Start 100274935:100274935(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.585A>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000370128
Start 100270620:100270620(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.354A>G
Mutation Classification Silent
Feature Type Transcript