Primary Site >> Stomach Cancer

Gene >> MNX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000252971
Start 157006520:157006520(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.811C>T
AA Mutation p.Arg271Cys(p.R271C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000252971
Start 157005696:157005696(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1030A>G
AA Mutation p.Ser344Gly(p.S344G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000252971
Start 157005657:157005657(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1069G>A
AA Mutation p.Glu357Lys(p.E357K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000252971
Start 157005832:157005832(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.894C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000252971
Start 157005607:157005607(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772480927
CDS Mutation c.1119C>T
Mutation Classification Silent
Feature Type Transcript