Primary Site >> Stomach Cancer

Gene >> CPB2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000181383
Start 46064654:46064654(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.790T>C
AA Mutation p.Trp264Arg(p.W264R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000181383
Start 46064707:46064707(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374776365
CDS Mutation c.737C>T
AA Mutation p.Ala246Val(p.A246V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000181383
Start 46064737:46064737(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.707G>A
AA Mutation p.Arg236Gln(p.R236Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000181383
Start 46053709:46053709(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773350527
CDS Mutation c.1177G>A
AA Mutation p.Gly393Arg(p.G393R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000181383
Start 46078811:46078811(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.475T>C
AA Mutation p.Tyr159His(p.Y159H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000181383
Start 46104963:46104963(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.47G>A
AA Mutation p.Cys16Tyr(p.C16Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000181383
Start 46058324:46058324(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.854C>T
AA Mutation p.Ser285Leu(p.S285L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000181383
Start 46082471:46082471(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs191429775
CDS Mutation c.354G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000181383
Start 46064682:46064682(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.762C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000181383
Start 46084281:46084281(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.213delT
AA Mutation p.Phe71LeufsTer2(p.F71Lfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000181383
Start 46084296:46084296(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.198delA
AA Mutation p.Lys66AsnfsTer7(p.K66Nfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000181383
Start 46084280:46084281(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.213dupT
AA Mutation p.Val72CysfsTer5(p.V72Cfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 13
Mutation Consequence splice_donor_variant
Transcription ID ENST00000181383
Start 46087743:46087743(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.150+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 14
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000181383
Start 46087821:46087821(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.75-1G>A
Mutation Classification Splice_Site
Feature Type Transcript
ID 15
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000181383
Start 46058382:46058382(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.797-1G>A
Mutation Classification Splice_Site
Feature Type Transcript