Primary Site >> Stomach Cancer

Gene >> OGG1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302036
Start 9765896:9765896(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1036G>A
AA Mutation p.Gly346Arg(p.G346R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000344629
Start 9756577:9756577(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750447639
CDS Mutation c.854C>T
AA Mutation p.Thr285Met(p.T285M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000344629
Start 9754741:9754741(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.603G>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000302036
Start 9765904:9765904(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1044G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000344629
Start 9750981:9750981(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.174A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000344629
Start 9750328:9750332(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.44_48delCTCTA
AA Mutation p.Thr15SerfsTer16(p.T15Sfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript