Primary Site >> Stomach Cancer

Gene >> WASL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000223023
Start 123748715:123748715(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779588397
CDS Mutation c.20A>C
AA Mutation p.Gln7Pro(p.Q7P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000223023
Start 123706817:123706817(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.262C>T
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000223023
Start 123692431:123692431(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1263delA
AA Mutation p.Val422TrpfsTer17(p.V422Wfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000223023
Start 123706326:123706326(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.387delA
AA Mutation p.Lys129AsnfsTer36(p.K129Nfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000223023
Start 123709108:123709108(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.233delT
AA Mutation p.Leu78Ter(p.L78*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000223023
Start 123692530:123692531(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1163dupC
AA Mutation p.Pro389AlafsTer6(p.P389Afs*6)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000223023
Start 123692430:123692431(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1263dupA
AA Mutation p.Val422SerfsTer31(p.V422Sfs*31)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000223023
Start 123694756:123694757(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.784dupA
AA Mutation p.Thr262AsnfsTer5(p.T262Nfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript