Primary Site >> Stomach Cancer

Gene >> RAB39B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369454
Start 155264201:155264201(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782719018
CDS Mutation c.88G>A
AA Mutation p.Glu30Lys(p.E30K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369454
Start 155261164:155261164(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782363257
CDS Mutation c.281G>A
AA Mutation p.Arg94His(p.R94H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369454
Start 155264261:155264261(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.28C>T
AA Mutation p.Arg10Trp(p.R10W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000369454
Start 155261031:155261031(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.414C>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000369454
Start 155261217:155261217(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.228C>T
Mutation Classification Silent
Feature Type Transcript