Primary Site >> Stomach Cancer

Gene >> WT1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000332351
Start 32392028:32392028(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1376A>C
AA Mutation p.Lys459Thr(p.K459T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000332351
Start 32417648:32417648(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.879T>G
AA Mutation p.Asn293Lys(p.N293K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000332351
Start 32428005:32428005(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.823G>A
AA Mutation p.Asp275Asn(p.D275N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000332351
Start 32389135:32389135(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1477T>C
AA Mutation p.Phe493Leu(p.F493L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000332351
Start 32428585:32428585(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs9332974
CDS Mutation c.681C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000332351
Start 32396324:32396324(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1182T>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000332351
Start 32434935:32434935(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.411C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000332351
Start 32399972:32399972(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1074G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000332351
Start 32428031:32428031(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.797delC
AA Mutation p.Pro266ArgfsTer20(p.P266Rfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript