Primary Site >> Stomach Cancer

Gene >> RGMB

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000513185
Start 98793338:98793338(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.899C>T
AA Mutation p.Ala300Val(p.A300V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000513185
Start 98793163:98793163(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749896271
CDS Mutation c.724G>A
AA Mutation p.Ala242Thr(p.A242T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000513185
Start 98779799:98779799(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.356G>T
AA Mutation p.Arg119Met(p.R119M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000513185
Start 98793299:98793299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.860G>A
AA Mutation p.Arg287His(p.R287H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000513185
Start 98779587:98779587(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.144C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000513185
Start 98793084:98793084(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.646-1G>C
Mutation Classification Splice_Site
Feature Type Transcript