Primary Site >> Stomach Cancer

Gene >> RAB33B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000305626
Start 139473037:139473037(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.601A>G
AA Mutation p.Ser201Gly(p.S201G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000305626
Start 139472944:139472944(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.508C>T
AA Mutation p.His170Tyr(p.H170Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000305626
Start 139454390:139454390(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.195G>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000305626
Start 139473064:139473064(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.632delC
AA Mutation p.Pro211LeufsTer7(p.P211Lfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence inframe_deletion
Transcription ID ENST00000305626
Start 139454213:139454251(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.21_59delGTCGCTCGAGGCAAGCTTTTCGTCCAGCGGGGCAGTGTC
AA Mutation p.Ser8_Ser20del(p.S8_S20del)
Mutation Classification In_Frame_Del
Feature Type Transcript