Primary Site >> Stomach Cancer

Gene >> LBP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000217407
Start 38369130:38369130(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1117T>A
AA Mutation p.Ser373Thr(p.S373T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000217407
Start 38369099:38369099(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1086G>A
AA Mutation p.Met362Ile(p.M362I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000217407
Start 38364032:38364032(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764270327
CDS Mutation c.710G>A
AA Mutation p.Arg237Gln(p.R237Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000217407
Start 38371320:38371320(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1258A>G
AA Mutation p.Asn420Asp(p.N420D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000217407
Start 38349598:38349598(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.175C>A
AA Mutation p.Leu59Met(p.L59M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000217407
Start 38346621:38346621(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.105C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant;start_lost
Transcription ID ENST00000217407
Start 38346519:38346519(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7delG
AA Mutation p.Ala3ProfsTer46(p.A3Pfs*46)
Mutation Classification Frame_Shift_Del
Feature Type Transcript