Primary Site >> Stomach Cancer

Gene >> PLA2G4A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367466
Start 186893146:186893146(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.251A>C
AA Mutation p.Glu84Ala(p.E84A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367466
Start 186979414:186979414(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2060A>G
AA Mutation p.Asn687Ser(p.N687S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000367466
Start 186911265:186911265(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.434G>A
AA Mutation p.Arg145Gln(p.R145Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000367466
Start 186950678:186950678(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1286T>C
AA Mutation p.Ile429Thr(p.I429T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000367466
Start 186950703:186950703(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1311T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000367466
Start 186893096:186893096(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.203delA
AA Mutation p.Asn68ThrfsTer24(p.N68Tfs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000367466
Start 186946717:186946717(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1119delT
AA Mutation p.Phe373LeufsTer17(p.F373Lfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000367466
Start 186939080:186939081(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.773dupA
AA Mutation p.Asn258LysfsTer3(p.N258Kfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript