Primary Site >> Stomach Cancer

Gene >> UGT2B15

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000338206
Start 68647374:68647374(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1323G>T
AA Mutation p.Glu441Asp(p.E441D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000338206
Start 68647211:68647211(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1486G>T
AA Mutation p.Ala496Ser(p.A496S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000338206
Start 68647190:68647190(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370288795
CDS Mutation c.1507G>A
AA Mutation p.Ala503Thr(p.A503T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000338206
Start 68654195:68654195(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1155C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000338206
Start 68670439:68670439(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.180T>C
Mutation Classification Silent
Feature Type Transcript