Primary Site >> Stomach Cancer

Gene >> HELQ

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295488
Start 83426046:83426046(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2723G>A
AA Mutation p.Gly908Glu(p.G908E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295488
Start 83421672:83421672(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2840A>T
AA Mutation p.Glu947Val(p.E947V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295488
Start 83448878:83448878(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1096A>C
AA Mutation p.Thr366Pro(p.T366P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000295488
Start 83453783:83453783(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.460A>G
AA Mutation p.Lys154Glu(p.K154E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000295488
Start 83453646:83453646(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.597G>T
AA Mutation p.Gln199His(p.Q199H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000295488
Start 83429596:83429596(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2446A>T
AA Mutation p.Thr816Ser(p.T816S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000295488
Start 83453824:83453824(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.419C>T
AA Mutation p.Ala140Val(p.A140V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000295488
Start 83446907:83446907(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1320delA
AA Mutation p.Gly441AspfsTer5(p.G441Dfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000295488
Start 83429615:83429615(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2427delA
AA Mutation p.Gly810AspfsTer33(p.G810Dfs*33)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000295488
Start 83453431:83453431(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.812delA
AA Mutation p.Asn271MetfsTer3(p.N271Mfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript