Primary Site >> Stomach Cancer

Gene >> POTEF

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357462
Start 130075023:130075023(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2449G>A
AA Mutation p.Glu817Lys(p.E817K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357462
Start 130075361:130075361(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2111A>T
AA Mutation p.Asp704Val(p.D704V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357462
Start 130074842:130074842(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757139860
CDS Mutation c.2630G>A
AA Mutation p.Arg877His(p.R877H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000357462
Start 130075089:130075089(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2383C>T
AA Mutation p.Arg795Cys(p.R795C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000357462
Start 130075007:130075007(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2465T>G
AA Mutation p.Ile822Ser(p.I822S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000357462
Start 130074394:130074394(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3078G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000357462
Start 130110578:130110578(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1020G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000357462
Start 130120162:130120162(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747331658
CDS Mutation c.354C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000357462
Start 130074477:130074477(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2995C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000357462
Start 130120336:130120336(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.180G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000357462
Start 130075416:130075416(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2056delA
AA Mutation p.Arg686GlyfsTer6(p.R686Gfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000357462
Start 130075289:130075290(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2182dupC
AA Mutation p.Arg728ProfsTer54(p.R728Pfs*54)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript