Primary Site >> Stomach Cancer

Gene >> RBBP4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000373493
Start 32668826:32668826(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.572G>T
AA Mutation p.Gly191Val(p.G191V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000373493
Start 32668332:32668332(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.418A>G
AA Mutation p.Ile140Val(p.I140V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000373493
Start 32668799:32668799(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.545G>A
AA Mutation p.Gly182Glu(p.G182E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000373493
Start 32669015:32669015(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs77147900
CDS Mutation c.644A>G
AA Mutation p.Lys215Arg(p.K215R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000373493
Start 32668850:32668850(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.596A>G
AA Mutation p.Asp199Gly(p.D199G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000373493
Start 32652006:32652006(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.109A>G
AA Mutation p.Thr37Ala(p.T37A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence splice_donor_variant;splice_acceptor_variant;intron_variant
Transcription ID ENST00000373493
Start 32669133:32669230(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.762-1_761+1delGTGAGTAGAATCCATTCAGAGTTTCTAAATATCTTGTCTAAGTTTTATGTTTAGTCACCATTTCAAGGTTTTTTTCCTTTGTTTTTTTTTCACTGAAG
Mutation Classification Splice_Site
Feature Type Transcript