Primary Site >> Stomach Cancer

Gene >> GSTO2

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000338595
Start 104279371:104279371(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.368T>C
AA Mutation p.Val123Ala(p.V123A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000338595
Start 104278102:104278102(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.352G>A
AA Mutation p.Glu118Lys(p.E118K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000338595
Start 104299261:104299261(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753712668
CDS Mutation c.709G>A
AA Mutation p.Ala237Thr(p.A237T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000338595
Start 104299171:104299171(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.619A>T
AA Mutation p.Met207Leu(p.M207L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000338595
Start 104299175:104299175(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.623A>C
AA Mutation p.Lys208Thr(p.K208T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000338595
Start 104299276:104299276(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.724C>T
Mutation Classification Silent
Feature Type Transcript