Primary Site >> Stomach Cancer

Gene >> LAP3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000226299
Start 17577553:17577553(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759168500
CDS Mutation c.88G>A
AA Mutation p.Ala30Thr(p.A30T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000226299
Start 17588868:17588868(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.754G>A
AA Mutation p.Ala252Thr(p.A252T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000226299
Start 17585100:17585100(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.668T>A
AA Mutation p.Leu223His(p.L223H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000226299
Start 17607571:17607571(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1542C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000226299
Start 17606930:17606930(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1362A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000226299
Start 17583603:17583603(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.506delA
AA Mutation p.Lys169ArgfsTer34(p.K169Rfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript