Primary Site >> Stomach Cancer

Gene >> DPP4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360534
Start 162018755:162018755(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1394C>T
AA Mutation p.Ala465Val(p.A465V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360534
Start 162017117:162017117(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1459A>C
AA Mutation p.Asn487His(p.N487H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360534
Start 162018783:162018783(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1366T>C
AA Mutation p.Tyr456His(p.Y456H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360534
Start 162035181:162035181(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs182689048
CDS Mutation c.757C>T
AA Mutation p.Arg253Trp(p.R253W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360534
Start 162035280:162035280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.658G>A
AA Mutation p.Gly220Ser(p.G220S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360534
Start 162035250:162035250(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.688G>A
AA Mutation p.Asp230Asn(p.D230N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000360534
Start 162073448:162073448(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.45T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000360534
Start 162039000:162039000(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.441G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000360534
Start 162035269:162035270(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.668dupT
AA Mutation p.Leu223PhefsTer7(p.L223Ffs*7)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript