Primary Site >> Stomach Cancer

Gene >> PDXK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000291565
Start 43755722:43755722(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145229797
CDS Mutation c.784A>G
AA Mutation p.Thr262Ala(p.T262A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000291565
Start 43741721:43741721(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.197A>G
AA Mutation p.Tyr66Cys(p.Y66C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000291565
Start 43743731:43743731(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144786200
CDS Mutation c.255G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000291565
Start 43749060:43749060(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746984644
CDS Mutation c.444G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence splice_donor_variant
Transcription ID ENST00000291565
Start 43743809:43743809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.331+2T>C
Mutation Classification Splice_Site
Feature Type Transcript