Primary Site >> Stomach Cancer

Gene >> ITGB1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302278
Start 32929906:32929906(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.292C>T
AA Mutation p.Arg98Cys(p.R98C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302278
Start 32920002:32920002(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201228879
CDS Mutation c.1352C>T
AA Mutation p.Thr451Met(p.T451M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302278
Start 32908406:32908406(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2293A>G
AA Mutation p.Lys765Glu(p.K765E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302278
Start 32920382:32920382(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1132C>A
AA Mutation p.Leu378Ile(p.L378I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000302278
Start 32912000:32912000(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202115007
CDS Mutation c.1594G>A
AA Mutation p.Val532Ile(p.V532I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000302278
Start 32925938:32925938(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371485643
CDS Mutation c.719G>A
AA Mutation p.Arg240His(p.R240H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000302278
Start 32911657:32911657(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1722C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence splice_donor_variant
Transcription ID ENST00000302278
Start 32925869:32925869(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.786+2T>C
Mutation Classification Splice_Site
Feature Type Transcript