Primary Site >> Stomach Cancer

Gene >> XPA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375128
Start 97687238:97687238(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.413T>G
AA Mutation p.Leu138Arg(p.L138R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375128
Start 97693742:97693742(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.190G>A
AA Mutation p.Ala64Thr(p.A64T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375128
Start 97685036:97685036(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.560T>C
AA Mutation p.Val187Ala(p.V187A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000375128
Start 97693753:97693753(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.179C>A
AA Mutation p.Ala60Asp(p.A60D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000375128
Start 97687240:97687240(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.411G>A
Mutation Classification Silent
Feature Type Transcript