Primary Site >> Stomach Cancer

Gene >> FPR3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000339223
Start 51824635:51824635(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.887G>A
AA Mutation p.Cys296Tyr(p.C296Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000339223
Start 51824627:51824627(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776156120
CDS Mutation c.879T>A
AA Mutation p.Phe293Leu(p.F293L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000339223
Start 51824668:51824668(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746950422
CDS Mutation c.920G>A
AA Mutation p.Arg307His(p.R307H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000339223
Start 51824692:51824692(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781059093
CDS Mutation c.944G>A
AA Mutation p.Arg315His(p.R315H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000339223
Start 51824792:51824792(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1044G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000339223
Start 51824324:51824324(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147264707
CDS Mutation c.576C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000339223
Start 51824030:51824030(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.282C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000339223
Start 51824465:51824481(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.719_735delTACGTGTCTTCGCTGCT
AA Mutation p.Leu240CysfsTer13(p.L240Cfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000339223
Start 51824622:51824622(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.879delT
AA Mutation p.Phe293LeufsTer21(p.F293Lfs*21)
Mutation Classification Frame_Shift_Del
Feature Type Transcript