Primary Site >> Stomach Cancer

Gene >> TOP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361337
Start 41114019:41114019(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1502C>T
AA Mutation p.Thr501Ile(p.T501I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361337
Start 41084538:41084538(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.584C>T
AA Mutation p.Pro195Leu(p.P195L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361337
Start 41122079:41122079(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2119G>C
AA Mutation p.Asp707His(p.D707H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361337
Start 41100164:41100164(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1084C>T
AA Mutation p.Arg362Cys(p.R362C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000361337
Start 41081188:41081188(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.455T>A
AA Mutation p.Ile152Asn(p.I152N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000361337
Start 41061465:41061465(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751834546
CDS Mutation c.130C>T
AA Mutation p.Arg44Trp(p.R44W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000361337
Start 41112855:41112855(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1382A>G
AA Mutation p.Tyr461Cys(p.Y461C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000361337
Start 41097315:41097315(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.830delA
AA Mutation p.Asn277IlefsTer10(p.N277Ifs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000361337
Start 41092540:41092540(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.686delC
AA Mutation p.Pro229HisfsTer19(p.P229Hfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000361337
Start 41100206:41100206(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1126C>T
AA Mutation p.Arg376Ter(p.R376*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence splice_donor_variant
Transcription ID ENST00000361337
Start 41098339:41098339(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.975+2T>C
Mutation Classification Splice_Site
Feature Type Transcript