Primary Site >> Stomach Cancer

Gene >> ZNF165

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000377325
Start 28089388:28089388(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1376G>T
AA Mutation p.Ser459Ile(p.S459I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000377325
Start 28088701:28088701(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.689C>T
AA Mutation p.Ala230Val(p.A230V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000377325
Start 28089378:28089378(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1366T>A
AA Mutation p.Tyr456Asn(p.Y456N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000377325
Start 28088782:28088782(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.770A>G
AA Mutation p.Lys257Arg(p.K257R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000377325
Start 28085867:28085867(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.387A>C
AA Mutation p.Arg129Ser(p.R129S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000377325
Start 28089140:28089140(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1128A>T
AA Mutation p.Glu376Asp(p.E376D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000377325
Start 28088829:28088829(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774158679
CDS Mutation c.817G>A
AA Mutation p.Asp273Asn(p.D273N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000377325
Start 28085793:28085793(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.313T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000377325
Start 28089290:28089290(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1278A>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000377325
Start 28088605:28088605(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.597delT
AA Mutation p.Phe199LeufsTer35(p.F199Lfs*35)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence inframe_deletion
Transcription ID ENST00000377325
Start 28088984:28089019(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.973_1008delTCTTTCAAGAGCCCAAAACTTGCTAAACATGCAGCA
AA Mutation p.Ser325_Ala336del(p.S325_A336del)
Mutation Classification In_Frame_Del
Feature Type Transcript