Primary Site >> Stomach Cancer

Gene >> LRRC32

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000260061
Start 76661166:76661166(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369688581
CDS Mutation c.427C>T
AA Mutation p.Arg143Trp(p.R143W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000260061
Start 76659638:76659638(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367700341
CDS Mutation c.1955G>A
AA Mutation p.Arg652His(p.R652H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000260061
Start 76660719:76660719(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749558497
CDS Mutation c.874G>A
AA Mutation p.Ala292Thr(p.A292T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000260061
Start 76660688:76660688(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.905T>C
AA Mutation p.Leu302Pro(p.L302P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000260061
Start 76660181:76660181(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1412T>C
AA Mutation p.Leu471Pro(p.L471P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000260061
Start 76665909:76665909(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.46C>A
AA Mutation p.Leu16Met(p.L16M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000260061
Start 76660176:76660176(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1417C>A
AA Mutation p.Leu473Ile(p.L473I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000260061
Start 76660401:76660401(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1192C>A
AA Mutation p.Leu398Met(p.L398M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000260061
Start 76660612:76660612(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.981T>C
Mutation Classification Silent
Feature Type Transcript