Primary Site >> Stomach Cancer

Gene >> DPEP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261615
Start 89636280:89636280(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762596549
CDS Mutation c.254C>T
AA Mutation p.Thr85Met(p.T85M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261615
Start 89638206:89638206(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1220G>A
AA Mutation p.Cys407Tyr(p.C407Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261615
Start 89637277:89637277(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.665C>T
AA Mutation p.Ala222Val(p.A222V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000261615
Start 89635977:89635977(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.174G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000261615
Start 89630473:89630473(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371346042
CDS Mutation c.63C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000261615
Start 89637288:89637288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.676C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000261615
Start 89637230:89637230(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.622delG
AA Mutation p.Val208SerfsTer13(p.V208Sfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript