Primary Site >> Stomach Cancer

Gene >> ATF6B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375203
Start 32128204:32128204(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778902783
CDS Mutation c.4G>A
AA Mutation p.Ala2Thr(p.A2T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375203
Start 32119934:32119934(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.856G>T
AA Mutation p.Gly286Cys(p.G286C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375203
Start 32119935:32119935(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.855G>T
AA Mutation p.Gln285His(p.Q285H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000375203
Start 32126220:32126220(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.375G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000375203
Start 32119925:32119925(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759543441
CDS Mutation c.865C>T
AA Mutation p.Arg289Ter(p.R289*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript