Primary Site >> Stomach Cancer

Gene >> E2F5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000416274
Start 85213836:85213836(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1015T>G
AA Mutation p.Phe339Val(p.F339V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000416274
Start 85203172:85203172(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.423A>G
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000416274
Start 85209201:85209201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.675T>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000416274
Start 85202226:85202226(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs761281897
CDS Mutation c.320delA
AA Mutation p.Lys107SerfsTer11(p.K107Sfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000416274
Start 85202172:85202172(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.265delA
AA Mutation p.Arg89GlyfsTer10(p.R89Gfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript