Primary Site >> Stomach Cancer

Gene >> STAG2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000371144
Start 124086573:124086573(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3080C>A
AA Mutation p.Thr1027Asn(p.T1027N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371144
Start 124063141:124063141(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1757C>G
AA Mutation p.Thr586Ser(p.T586S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000371144
Start 124031025:124031025(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.188C>A
AA Mutation p.Pro63His(p.P63H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000371144
Start 124051212:124051212(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1109G>A
AA Mutation p.Arg370Gln(p.R370Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000371144
Start 124037567:124037567(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.329G>A
AA Mutation p.Arg110Gln(p.R110Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000371144
Start 124086656:124086656(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3163G>A
AA Mutation p.Asp1055Asn(p.D1055N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000371144
Start 124071281:124071281(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2491G>A
AA Mutation p.Asp831Asn(p.D831N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000371144
Start 124086710:124086710(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3217A>G
AA Mutation p.Lys1073Glu(p.K1073E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000371144
Start 124083456:124083456(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768937075
CDS Mutation c.2960C>A
AA Mutation p.Pro987Gln(p.P987Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000371144
Start 124062981:124062981(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1718A>G
AA Mutation p.Gln573Arg(p.Q573R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000371144
Start 124095429:124095429(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3652G>A
AA Mutation p.Ala1218Thr(p.A1218T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000371144
Start 124037577:124037577(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.339A>C
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000371144
Start 124068584:124068584(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2286G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000371144
Start 124083532:124083532(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3036A>G
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000371144
Start 124051180:124051180(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1077G>A
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000371144
Start 124030967:124030967(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.135delA
AA Mutation p.Gly46AlafsTer25(p.G46Afs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000371144
Start 124045223:124045223(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.526delT
AA Mutation p.Cys176ValfsTer7(p.C176Vfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000371144
Start 124042624:124042625(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.441_442insG
AA Mutation p.Met148AspfsTer3(p.M148Dfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript