Primary Site >> Stomach Cancer

Gene >> DENND2D

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357640
Start 111192288:111192288(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769717736
CDS Mutation c.824C>T
AA Mutation p.Ala275Val(p.A275V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357640
Start 111194620:111194620(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145056723
CDS Mutation c.752C>T
AA Mutation p.Ala251Val(p.A251V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000357640
Start 111192287:111192287(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs187119617
CDS Mutation c.825C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000357640
Start 111194625:111194625(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.747C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000357640
Start 111187615:111187616(version: GRCh38)
Mutation Type INS
dbSNP_RS rs765960547
CDS Mutation c.1405dupA
AA Mutation p.Thr469AsnfsTer13(p.T469Nfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript