Primary Site >> Stomach Cancer

Gene >> GATA3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000346208
Start 8073953:8073953(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1262C>A
AA Mutation p.Pro421Gln(p.P421Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000346208
Start 8058445:8058445(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.382G>A
AA Mutation p.Gly128Arg(p.G128R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000346208
Start 8073874:8073874(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200935603
CDS Mutation c.1183G>A
AA Mutation p.Ala395Thr(p.A395T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000346208
Start 8058745:8058745(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774889150
CDS Mutation c.682G>A
AA Mutation p.Glu228Lys(p.E228K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000346208
Start 8073950:8073950(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374919553
CDS Mutation c.1259C>T
AA Mutation p.Thr420Met(p.T420M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000346208
Start 8058678:8058678(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.615G>A
AA Mutation p.Met205Ile(p.M205I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000346208
Start 8073844:8073844(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1153T>G
AA Mutation p.Phe385Val(p.F385V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000346208
Start 8058388:8058388(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776412274
CDS Mutation c.325G>A
AA Mutation p.Ala109Thr(p.A109T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000346208
Start 8074012:8074012(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1321G>A
AA Mutation p.Ala441Thr(p.A441T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000346208
Start 8064129:8064129(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760084913
CDS Mutation c.912G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000346208
Start 8058600:8058600(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.537C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000346208
Start 8058507:8058507(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.444G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000346208
Start 8055886:8055886(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.231G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000346208
Start 8058765:8058765(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs776668722
CDS Mutation c.708delC
AA Mutation p.Ser237AlafsTer28(p.S237Afs*28)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000346208
Start 8058783:8058783(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.722delG
AA Mutation p.Gly241AlafsTer24(p.G241Afs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000346208
Start 8073817:8073817(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1131delA
AA Mutation p.Val378CysfsTer26(p.V378Cfs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000346208
Start 8058462:8058462(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.404delC
AA Mutation p.Pro135ArgfsTer60(p.P135Rfs*60)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000346208
Start 8064130:8064130(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.913C>T
AA Mutation p.Arg305Ter(p.R305*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript