Primary Site >> Stomach Cancer

Gene >> LCN2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000277480
Start 128149605:128149605(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.80T>C
AA Mutation p.Leu27Pro(p.L27P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000277480
Start 128149602:128149602(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.77A>G
AA Mutation p.Asp26Gly(p.D26G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000277480
Start 128151653:128151653(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.291C>A
AA Mutation p.Asp97Glu(p.D97E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000277480
Start 128151701:128151701(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777669542
CDS Mutation c.339G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000277480
Start 128151689:128151689(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767897190
CDS Mutation c.327C>T
Mutation Classification Silent
Feature Type Transcript