Primary Site >> Stomach Cancer

Gene >> C5AR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000355085
Start 47320687:47320687(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201031420
CDS Mutation c.910G>A
AA Mutation p.Gly304Ser(p.G304S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000355085
Start 47319979:47319979(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201947994
CDS Mutation c.202C>T
AA Mutation p.Arg68Trp(p.R68W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000355085
Start 47320171:47320171(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200066829
CDS Mutation c.394G>A
AA Mutation p.Ala132Thr(p.A132T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000355085
Start 47320736:47320736(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200226809
CDS Mutation c.959G>A
AA Mutation p.Arg320Gln(p.R320Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000355085
Start 47320494:47320494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.717G>T
AA Mutation p.Lys239Asn(p.K239N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000355085
Start 47320093:47320093(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750171124
CDS Mutation c.316G>A
AA Mutation p.Gly106Arg(p.G106R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000355085
Start 47320099:47320099(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.322G>A
AA Mutation p.Ala108Thr(p.A108T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000355085
Start 47319867:47319867(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.90T>C
Mutation Classification Silent
Feature Type Transcript