Primary Site >> Stomach Cancer

Gene >> NES

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368223
Start 156669887:156669887(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4301C>A
AA Mutation p.Ala1434Asp(p.A1434D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368223
Start 156671822:156671822(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2366A>C
AA Mutation p.Lys789Thr(p.K789T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368223
Start 156672472:156672472(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1716T>A
AA Mutation p.Asn572Lys(p.N572K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368223
Start 156671806:156671806(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2382G>T
AA Mutation p.Glu794Asp(p.E794D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368223
Start 156671574:156671574(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2614G>A
AA Mutation p.Glu872Lys(p.E872K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000368223
Start 156670432:156670432(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3756G>T
AA Mutation p.Arg1252Ser(p.R1252S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000368223
Start 156671133:156671133(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3055C>T
AA Mutation p.Pro1019Ser(p.P1019S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000368223
Start 156671420:156671420(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2768T>C
AA Mutation p.Leu923Pro(p.L923P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000368223
Start 156670836:156670836(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3352G>C
AA Mutation p.Glu1118Gln(p.E1118Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000368223
Start 156673463:156673463(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.973A>G
AA Mutation p.Ser325Gly(p.S325G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000368223
Start 156670921:156670921(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3267C>G
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000368223
Start 156672049:156672049(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2139T>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000368223
Start 156675281:156675281(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.843C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000368223
Start 156673012:156673012(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs759081520
CDS Mutation c.1176delC
AA Mutation p.Thr393HisfsTer9(p.T393Hfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000368223
Start 156670443:156670443(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3745delG
AA Mutation p.Val1249CysfsTer11(p.V1249Cfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000368223
Start 156677139:156677139(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.126delG
AA Mutation p.Leu43SerfsTer67(p.L43Sfs*67)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000368223
Start 156671901:156671901(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2287C>T
AA Mutation p.Gln763Ter(p.Q763*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000368223
Start 156672861:156672861(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1327G>T
AA Mutation p.Gly443Ter(p.G443*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript