Primary Site >> Stomach Cancer

Gene >> PPARG

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000287820
Start 12416869:12416869(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.985A>G
AA Mutation p.Lys329Glu(p.K329E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000287820
Start 12417074:12417074(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1190A>G
AA Mutation p.Glu397Gly(p.E397G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000287820
Start 12379798:12379798(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.177C>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000287820
Start 12392683:12392683(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.556delA
AA Mutation p.Ser186ValfsTer47(p.S186Vfs*47)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000287820
Start 12392752:12392753(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.619_619+1insCCATCAGGTTTGGGCGGATGCCACA
AA Mutation p.Gln215HisfsTer22(p.Q215Hfs*22)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript