Primary Site >> Stomach Cancer

Gene >> RND3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263895
Start 150470225:150470225(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 2
Mutation Consequence missense_variant
Transcription ID ENST00000263895
Start 150474972:150474972(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.251A>G
AA Mutation p.Tyr84Cys(p.Y84C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000263895
Start 150470167:150470167(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs564593926
CDS Mutation c.555C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000263895
Start 150470041:150470041(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769148948
CDS Mutation c.681G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000263895
Start 150474955:150474955(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.268delC
AA Mutation p.Leu90SerfsTer10(p.L90Sfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript