Primary Site >> Stomach Cancer

Gene >> ADRA1B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306675
Start 159917842:159917842(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.937G>T
AA Mutation p.Ala313Ser(p.A313S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000306675
Start 159917348:159917348(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758643818
CDS Mutation c.443G>A
AA Mutation p.Arg148His(p.R148H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000306675
Start 159972001:159972001(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1072G>A
AA Mutation p.Ala358Thr(p.A358T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000306675
Start 159972034:159972034(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1105G>A
AA Mutation p.Gly369Ser(p.G369S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000306675
Start 159917134:159917134(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs571519472
CDS Mutation c.229C>T
AA Mutation p.Arg77Trp(p.R77W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000306675
Start 159971979:159971979(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1050C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000306675
Start 159917841:159917841(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.936C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000306675
Start 159917082:159917082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.177C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000306675
Start 159971902:159971902(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.978delC
AA Mutation p.Asp327ThrfsTer88(p.D327Tfs*88)
Mutation Classification Frame_Shift_Del
Feature Type Transcript