Primary Site >> Stomach Cancer

Gene >> RHNO1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000489288
Start 2887978:2887978(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs539902874
CDS Mutation c.236C>T
AA Mutation p.Ala79Val(p.A79V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000489288
Start 2887981:2887981(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.239G>A
AA Mutation p.Arg80Lys(p.R80K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000489288
Start 2888080:2888080(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367602600
CDS Mutation c.338G>A
AA Mutation p.Arg113Gln(p.R113Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000489288
Start 2885528:2885528(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.162T>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000489288
Start 2885378:2885378(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.18delA
AA Mutation p.Lys6AsnfsTer89(p.K6Nfs*89)
Mutation Classification Frame_Shift_Del
Feature Type Transcript