Primary Site >> Stomach Cancer

Gene >> IL20RA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000316649
Start 137008674:137008674(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.649C>T
AA Mutation p.His217Tyr(p.H217Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000316649
Start 137002204:137002204(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1016T>G
AA Mutation p.Leu339Arg(p.L339R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000316649
Start 137009318:137009318(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142288648
CDS Mutation c.578C>T
AA Mutation p.Thr193Met(p.T193M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000316649
Start 137008640:137008640(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747471948
CDS Mutation c.683G>A
AA Mutation p.Arg228His(p.R228H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000316649
Start 137008677:137008677(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752578754
CDS Mutation c.646G>A
AA Mutation p.Val216Ile(p.V216I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000316649
Start 137001811:137001811(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1409G>T
AA Mutation p.Gly470Val(p.G470V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000316649
Start 137001891:137001891(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1329G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000316649
Start 137001657:137001657(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1563C>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000316649
Start 137002039:137002039(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1181delC
AA Mutation p.Pro394ArgfsTer64(p.P394Rfs*64)
Mutation Classification Frame_Shift_Del
Feature Type Transcript