Primary Site >> Stomach Cancer

Gene >> LSR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35250357:35250357(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.296A>G
AA Mutation p.His99Arg(p.H99R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35250327:35250327(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.266C>T
AA Mutation p.Ala89Val(p.A89V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35266367:35266367(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755518851
CDS Mutation c.931G>A
AA Mutation p.Ala311Thr(p.A311T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000361790
Start 35250394:35250394(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.333T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000361790
Start 35262556:35262556(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.786C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000361790
Start 35267641:35267641(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1821C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000361790
Start 35261944:35261944(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.738T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000361790
Start 35266942:35266942(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1269delC
AA Mutation p.Ser424ValfsTer8(p.S424Vfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000361790
Start 35267393:35267393(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1577delC
AA Mutation p.Pro526ArgfsTer70(p.P526Rfs*70)
Mutation Classification Frame_Shift_Del
Feature Type Transcript