Primary Site >> Stomach Cancer

Gene >> SUV39H2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000354919
Start 14896973:14896973(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.305C>A
AA Mutation p.Ser102Tyr(p.S102Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000354919
Start 14899633:14899633(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.944T>C
AA Mutation p.Phe315Ser(p.F315S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000354919
Start 14897018:14897018(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.350A>G
AA Mutation p.Lys117Arg(p.K117R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000354919
Start 14899680:14899680(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.991C>T
AA Mutation p.His331Tyr(p.H331Y)
Mutation Classification Missense_Mutation
Feature Type Transcript