Primary Site >> Stomach Cancer

Gene >> BBOX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263182
Start 27093329:27093329(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.496G>T
AA Mutation p.Gly166Trp(p.G166W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263182
Start 27127337:27127337(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1048C>T
AA Mutation p.Arg350Cys(p.R350C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263182
Start 27127337:27127337(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781597328
CDS Mutation c.1048C>G
AA Mutation p.Arg350Gly(p.R350G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000263182
Start 27093226:27093226(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.393A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000263182
Start 27119822:27119822(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.813A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000263182
Start 27125799:27125800(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.986_987insAAGTTAC
AA Mutation p.Phe330SerfsTer9(p.F330Sfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000263182
Start 27127292:27127292(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1004-1G>T
Mutation Classification Splice_Site
Feature Type Transcript