Primary Site >> Stomach Cancer

Gene >> PTPN4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263708
Start 119885842:119885842(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779166189
CDS Mutation c.635G>A
AA Mutation p.Arg212His(p.R212H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263708
Start 119900733:119900733(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.691G>A
AA Mutation p.Glu231Lys(p.E231K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263708
Start 119920112:119920112(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.872A>G
AA Mutation p.Tyr291Cys(p.Y291C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263708
Start 119955261:119955261(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770341394
CDS Mutation c.1918C>T
AA Mutation p.Arg640Trp(p.R640W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263708
Start 119934891:119934891(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140214166
CDS Mutation c.1288G>A
AA Mutation p.Glu430Lys(p.E430K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000263708
Start 119932535:119932535(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140598634
CDS Mutation c.1182G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000263708
Start 119920197:119920197(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.963delT
AA Mutation p.Phe321LeufsTer7(p.F321Lfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000263708
Start 119920190:119920190(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.953delA
AA Mutation p.Lys318ArgfsTer10(p.K318Rfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000263708
Start 119960881:119960881(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2212delT
AA Mutation p.Trp738GlyfsTer3(p.W738Gfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000263708
Start 119915190:119915191(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.781dupA
AA Mutation p.Ile261AsnfsTer4(p.I261Nfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000263708
Start 119920196:119920197(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.963dupT
AA Mutation p.Ala322CysfsTer17(p.A322Cfs*17)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript