Primary Site >> Stomach Cancer

Gene >> E2F8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000250024
Start 19234921:19234921(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.589G>A
AA Mutation p.Gly197Arg(p.G197R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000250024
Start 19235049:19235049(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.461G>A
AA Mutation p.Arg154His(p.R154H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000250024
Start 19229719:19229719(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1628C>T
AA Mutation p.Thr543Met(p.T543M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000250024
Start 19234750:19234750(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372105528
CDS Mutation c.760C>T
AA Mutation p.Arg254Trp(p.R254W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000250024
Start 19237866:19237866(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.282A>C
AA Mutation p.Lys94Asn(p.K94N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000250024
Start 19234446:19234446(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755274793
CDS Mutation c.842C>T
AA Mutation p.Thr281Met(p.T281M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000250024
Start 19237446:19237446(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.319G>C
AA Mutation p.Glu107Gln(p.E107Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000250024
Start 19230315:19230315(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1284G>T
AA Mutation p.Gln428His(p.Q428H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000250024
Start 19235029:19235029(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.481G>A
AA Mutation p.Val161Met(p.V161M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000250024
Start 19235024:19235024(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.486C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000250024
Start 19238090:19238090(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.58delA
AA Mutation p.Thr20HisfsTer3(p.T20Hfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000250024
Start 19229914:19229914(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1433delC
AA Mutation p.Pro478GlnfsTer2(p.P478Qfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000250024
Start 19230666:19230666(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1235delA
AA Mutation p.Asn412IlefsTer37(p.N412Ifs*37)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000250024
Start 19229679:19229679(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1668delA
AA Mutation p.Asp557ThrfsTer67(p.D557Tfs*67)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000250024
Start 19225807:19225807(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1951G>T
AA Mutation p.Glu651Ter(p.E651*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000250024
Start 19234882:19234882(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.628A>T
AA Mutation p.Lys210Ter(p.K210*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence splice_donor_variant
Transcription ID ENST00000250024
Start 19232232:19232232(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1066+2T>C
Mutation Classification Splice_Site
Feature Type Transcript