Primary Site >> Stomach Cancer

Gene >> CUL2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374748
Start 35010339:35010339(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202046289
CDS Mutation c.2210C>T
AA Mutation p.Ser737Leu(p.S737L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374748
Start 35029556:35029556(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1471A>C
AA Mutation p.Asn491His(p.N491H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000374748
Start 35011928:35011928(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2026C>T
AA Mutation p.Arg676Trp(p.R676W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000374748
Start 35028880:35028880(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1547C>A
AA Mutation p.Ala516Glu(p.A516E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000374748
Start 35062988:35062988(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.194delT
AA Mutation p.Leu65TrpfsTer54(p.L65Wfs*54)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000374748
Start 35029557:35029558(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1469_1470insAGGACTTTAGAAG
AA Mutation p.Phe490LeufsTer4(p.F490Lfs*4)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000374748
Start 35062987:35062988(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.194dupT
AA Mutation p.Leu65PhefsTer10(p.L65Ffs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript