Primary Site >> Stomach Cancer

Gene >> BVES

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000314641
Start 105115793:105115793(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.851G>A
AA Mutation p.Cys284Tyr(p.C284Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000314641
Start 105125433:105125433(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.497A>G
AA Mutation p.Lys166Arg(p.K166R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000314641
Start 105129399:105129399(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760966564
CDS Mutation c.331C>A
AA Mutation p.Leu111Ile(p.L111I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000314641
Start 105125544:105125544(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148128379
CDS Mutation c.386G>A
AA Mutation p.Arg129Gln(p.R129Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000314641
Start 105101134:105101134(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1038delT
AA Mutation p.Phe346LeufsTer9(p.F346Lfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000314641
Start 105129468:105129468(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs796206315
CDS Mutation c.262C>T
AA Mutation p.Arg88Ter(p.R88*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript