Primary Site >> Stomach Cancer

Gene >> IPP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000396478
Start 45727640:45727640(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767500416
CDS Mutation c.1039G>A
AA Mutation p.Ala347Thr(p.A347T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000396478
Start 45746314:45746314(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.98G>A
AA Mutation p.Gly33Glu(p.G33E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000396478
Start 45741247:45741247(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.378C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000396478
Start 45741316:45741316(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.309T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000396478
Start 45740915:45740915(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.710delT
AA Mutation p.Leu237Ter(p.L237*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript