Primary Site >> Stomach Cancer

Gene >> PAK2

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000327134
Start 196820567:196820567(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1350G>T
AA Mutation p.Arg450Ser(p.R450S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000327134
Start 196827281:196827281(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759691640
CDS Mutation c.1436G>A
AA Mutation p.Arg479Gln(p.R479Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000327134
Start 196803086:196803086(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.358C>T
AA Mutation p.Pro120Ser(p.P120S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000327134
Start 196820502:196820502(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1285C>A
AA Mutation p.Leu429Met(p.L429M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000327134
Start 196806629:196806629(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs565026135
CDS Mutation c.519T>G
AA Mutation p.Asp173Glu(p.D173E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000327134
Start 196827236:196827236(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1391A>G
AA Mutation p.Gln464Arg(p.Q464R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000327134
Start 196812238:196812238(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.793A>G
AA Mutation p.Thr265Ala(p.T265A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000327134
Start 196820415:196820415(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1198C>T
AA Mutation p.Arg400Cys(p.R400C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000327134
Start 196807826:196807826(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758114223
CDS Mutation c.621T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000327134
Start 196810638:196810638(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.763delA
AA Mutation p.Ile255LeufsTer36(p.I255Lfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000327134
Start 196814497:196814497(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.987delG
AA Mutation p.Ser330HisfsTer6(p.S330Hfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000327134
Start 196827308:196827308(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1466delG
AA Mutation p.Gly489ValfsTer12(p.G489Vfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000327134
Start 196812218:196812218(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.774-1G>A
Mutation Classification Splice_Site
Feature Type Transcript