Primary Site >> Stomach Cancer

Gene >> TAF1D

ID 1
Mutation Consequence missense_variant;NMD_transcript_variant
Transcription ID ENST00000323981
Start 93738496:93738496(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.72T>A
AA Mutation p.Asp24Glu(p.D24E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;NMD_transcript_variant
Transcription ID ENST00000323981
Start 93736262:93736262(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.736A>G
AA Mutation p.Ser246Gly(p.S246G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;NMD_transcript_variant
Transcription ID ENST00000323981
Start 93738442:93738442(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.126A>C
AA Mutation p.Lys42Asn(p.K42N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant;NMD_transcript_variant
Transcription ID ENST00000323981
Start 93738262:93738262(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.306A>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant;NMD_transcript_variant
Transcription ID ENST00000323981
Start 93737216:93737216(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.483delT
AA Mutation p.Phe161LeufsTer7(p.F161Lfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant;NMD_transcript_variant
Transcription ID ENST00000323981
Start 93738287:93738287(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs746556335
CDS Mutation c.281delA
AA Mutation p.Lys94ArgfsTer26(p.K94Rfs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript