Primary Site >> Stomach Cancer

Gene >> TUBB2A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000333628
Start 3154459:3154459(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.742G>A
AA Mutation p.Ala248Thr(p.A248T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000333628
Start 3154563:3154563(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.638G>A
AA Mutation p.Arg213His(p.R213H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000333628
Start 3154564:3154564(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.637C>T
AA Mutation p.Arg213Cys(p.R213C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000333628
Start 3154521:3154521(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.680A>G
AA Mutation p.His227Arg(p.H227R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000333628
Start 3157450:3157450(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.14T>C
AA Mutation p.Val5Ala(p.V5A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000333628
Start 3154583:3154583(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.618C>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000333628
Start 3153908:3153908(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1293C>T
Mutation Classification Silent
Feature Type Transcript