Primary Site >> Stomach Cancer

Gene >> TP53BP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000343537
Start 223802191:223802191(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1150A>G
AA Mutation p.Ile384Val(p.I384V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000343537
Start 223802323:223802323(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1018C>T
AA Mutation p.Pro340Ser(p.P340S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000343537
Start 223800807:223800807(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1229C>A
AA Mutation p.Ser410Tyr(p.S410Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000343537
Start 223798506:223798506(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1657G>A
AA Mutation p.Ala553Thr(p.A553T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000343537
Start 223796260:223796260(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2279A>G
AA Mutation p.Tyr760Cys(p.Y760C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000343537
Start 223800002:223800002(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762131208
CDS Mutation c.1382G>A
AA Mutation p.Arg461His(p.R461H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000343537
Start 223821360:223821360(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.35T>C
AA Mutation p.Leu12Pro(p.L12P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000343537
Start 223796301:223796301(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2238G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000343537
Start 223789150:223789150(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3021A>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000343537
Start 223804229:223804229(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.594delA
AA Mutation p.Val199Ter(p.V199*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000343537
Start 223814254:223814254(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.275delC
AA Mutation p.Pro92LeufsTer6(p.P92Lfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000343537
Start 223784219:223784219(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3259G>T
AA Mutation p.Gly1087Ter(p.G1087*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000343537
Start 223798279:223798280(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1883dupA
AA Mutation p.Asn628LysfsTer26(p.N628Kfs*26)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript