Primary Site >> Stomach Cancer

Gene >> HS6ST2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370836
Start 132628920:132628920(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1121C>T
AA Mutation p.Pro374Leu(p.P374L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370836
Start 132628840:132628840(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1201G>T
AA Mutation p.Gly401Cys(p.G401C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370836
Start 132958242:132958242(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.361G>A
AA Mutation p.Ala121Thr(p.A121T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370836
Start 132628570:132628570(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1471G>A
AA Mutation p.Ala491Thr(p.A491T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370836
Start 132957136:132957136(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768825303
CDS Mutation c.619C>T
AA Mutation p.Arg207Cys(p.R207C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000370836
Start 132957100:132957100(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.655G>A
AA Mutation p.Val219Ile(p.V219I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000370836
Start 132956938:132956938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.817C>T
AA Mutation p.Arg273Trp(p.R273W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000370836
Start 132957080:132957080(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.675C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000370836
Start 132628967:132628967(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1074C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000370836
Start 132957136:132957136(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.619delC
AA Mutation p.Arg207AlafsTer13(p.R207Afs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000370836
Start 132628553:132628554(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1487dupT
AA Mutation p.Leu496PhefsTer93(p.L496Ffs*93)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript