Primary Site >> Stomach Cancer

Gene >> LILRB2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000391749
Start 54279608:54279608(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.395C>A
AA Mutation p.Pro132His(p.P132H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000391749
Start 54278436:54278436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138762759
CDS Mutation c.1082C>T
AA Mutation p.Ala361Val(p.A361V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000391749
Start 54279546:54279546(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.457T>C
AA Mutation p.Phe153Leu(p.F153L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000391749
Start 54276394:54276394(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1546G>A
AA Mutation p.Gly516Ser(p.G516S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000391749
Start 54278270:54278270(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759753568
CDS Mutation c.1248C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000391749
Start 54279424:54279424(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370713732
CDS Mutation c.579G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000391749
Start 54279837:54279837(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs541426329
CDS Mutation c.309C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000391749
Start 54279580:54279580(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780942118
CDS Mutation c.423C>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000391749
Start 54278488:54278488(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1030C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000391749
Start 54279084:54279087(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.680_683delTCTC
AA Mutation p.Leu227GlnfsTer14(p.L227Qfs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript