Primary Site >> Pancreatic Cancer

Gene >> CTNNA2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000402739
Start 79858033:79858033(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.319T>G
AA Mutation p.Ser107Ala(p.S107A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000402739
Start 79874190:79874190(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371032975
CDS Mutation c.700G>A
AA Mutation p.Ala234Thr(p.A234T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000402739
Start 80647802:80647802(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs529691509
CDS Mutation c.2792G>A
AA Mutation p.Arg931Gln(p.R931Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000402739
Start 79909753:79909753(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1012G>A
AA Mutation p.Val338Met(p.V338M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000402739
Start 80419589:80419589(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1278C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000402739
Start 80619201:80619201(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2547C>T
Mutation Classification Silent
Feature Type Transcript