Primary Site >> Stomach Cancer

Gene >> PBX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000420696
Start 164807619:164807619(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.779A>G
AA Mutation p.Tyr260Cys(p.Y260C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000420696
Start 164799799:164799799(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.611T>C
AA Mutation p.Ile204Thr(p.I204T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000420696
Start 164799735:164799735(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.547C>A
AA Mutation p.Leu183Met(p.L183M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000420696
Start 164846587:164846587(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1204A>G
AA Mutation p.Asn402Asp(p.N402D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000420696
Start 164799886:164799886(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.698C>T
AA Mutation p.Ala233Val(p.A233V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000420696
Start 164792732:164792732(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143132748
CDS Mutation c.504C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000420696
Start 164846595:164846595(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1212T>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000420696
Start 164792627:164792627(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.399G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000420696
Start 164792493:164792493(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.266-1G>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 10
Mutation Consequence inframe_insertion;splice_region_variant
Transcription ID ENST00000420696
Start 164563311:164563312(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.265_265+1insTTTTGA
AA Mutation p.Leu90_Ser91insIleLeu(p.L90_S91insIL)
Mutation Classification In_Frame_Ins
Feature Type Transcript