Primary Site >> Stomach Cancer

Gene >> OLIG2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000333337
Start 33027124:33027124(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768519339
CDS Mutation c.262T>G
AA Mutation p.Ser88Ala(p.S88A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000333337
Start 33027019:33027019(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.157G>A
AA Mutation p.Ala53Thr(p.A53T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000333337
Start 33027083:33027083(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.221G>A
AA Mutation p.Gly74Asp(p.G74D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000333337
Start 33026952:33026952(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.90C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000333337
Start 33027099:33027099(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.237G>A
Mutation Classification Silent
Feature Type Transcript