Primary Site >> Stomach Cancer

Gene >> LRRC4C

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000278198
Start 40116058:40116058(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754463669
CDS Mutation c.235C>T
AA Mutation p.Arg79Trp(p.R79W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000278198
Start 40115167:40115167(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749582918
CDS Mutation c.1126C>T
AA Mutation p.Arg376Trp(p.R376W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000278198
Start 40116106:40116106(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.187G>T
AA Mutation p.Val63Phe(p.V63F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000278198
Start 40115956:40115956(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.337A>G
AA Mutation p.Arg113Gly(p.R113G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000278198
Start 40114827:40114827(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1466T>C
AA Mutation p.Val489Ala(p.V489A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000278198
Start 40114937:40114937(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1356T>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000278198
Start 40115363:40115363(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.930G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000278198
Start 40114463:40114463(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1830A>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000278198
Start 40115156:40115156(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1137A>G
Mutation Classification Silent
Feature Type Transcript