Primary Site >> Stomach Cancer

Gene >> RHOJ

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000316754
Start 63290894:63290894(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779493646
CDS Mutation c.515A>G
AA Mutation p.Tyr172Cys(p.Y172C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000316754
Start 63283215:63283215(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.497C>T
AA Mutation p.Ala166Val(p.A166V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000316754
Start 63204918:63204918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.49G>A
AA Mutation p.Asp17Asn(p.D17N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000316754
Start 63269160:63269160(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.229G>A
AA Mutation p.Ala77Thr(p.A77T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000316754
Start 63269162:63269162(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148425776
CDS Mutation c.231G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000316754
Start 63204902:63204902(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.33C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000316754
Start 63290996:63290997(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.620dupG
AA Mutation p.His208SerfsTer21(p.H208Sfs*21)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript