Primary Site >> Stomach Cancer

Gene >> CRADD

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000332896
Start 93850167:93850167(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779660963
CDS Mutation c.496C>T
AA Mutation p.Arg166Cys(p.R166C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000332896
Start 93850174:93850174(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs563879626
CDS Mutation c.503G>A
AA Mutation p.Arg168Gln(p.R168Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000332896
Start 93678811:93678811(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759429176
CDS Mutation c.37C>T
AA Mutation p.Arg13Cys(p.R13C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000332896
Start 93850217:93850217(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs544159440
CDS Mutation c.546C>T
Mutation Classification Silent
Feature Type Transcript