Primary Site >> Stomach Cancer

Gene >> SELENBP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368868
Start 151365806:151365806(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781731476
CDS Mutation c.884C>T
AA Mutation p.Pro295Leu(p.P295L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368868
Start 151365777:151365777(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs571013649
CDS Mutation c.913G>A
AA Mutation p.Glu305Lys(p.E305K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368868
Start 151364565:151364565(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1397G>A
AA Mutation p.Cys466Tyr(p.C466Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368868
Start 151365791:151365791(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757948741
CDS Mutation c.899G>A
AA Mutation p.Gly300Asp(p.G300D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368868
Start 151366430:151366430(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750981873
CDS Mutation c.688G>A
AA Mutation p.Val230Ile(p.V230I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000368868
Start 151369459:151369459(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.157T>C
AA Mutation p.Ser53Pro(p.S53P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000368868
Start 151364645:151364645(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1317C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000368868
Start 151369089:151369092(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.272_275delGCAC
AA Mutation p.Arg91ProfsTer56(p.R91Pfs*56)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained;protein_altering_variant
Transcription ID ENST00000368868
Start 151365603:151365604(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1003_1004insCTGCTTTAAATGGGAAAACAACGTAGGAGC
AA Mutation p.Tyr335delinsSerAlaLeuAsnGlyLysThrThrTerGluHis(p.Y335delinsSALNGKTT*EH)
Mutation Classification Nonsense_Mutation
Feature Type Transcript