Primary Site >> Stomach Cancer

Gene >> DPPA2

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000478945
Start 109304668:109304668(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199811743
CDS Mutation c.661G>A
AA Mutation p.Val221Ile(p.V221I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000478945
Start 109309051:109309051(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.371G>T
AA Mutation p.Arg124Met(p.R124M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000478945
Start 109309325:109309325(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.187C>A
AA Mutation p.Leu63Ile(p.L63I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000478945
Start 109308242:109308242(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779719606
CDS Mutation c.448C>T
AA Mutation p.Arg150Cys(p.R150C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000478945
Start 109304613:109304613(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.716T>C
AA Mutation p.Val239Ala(p.V239A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000478945
Start 109309308:109309308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.204G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000478945
Start 109312676:109312677(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.49dupG
AA Mutation p.Glu17GlyfsTer4(p.E17Gfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript