Primary Site >> Stomach Cancer

Gene >> SIM2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000290399
Start 36726236:36726236(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.661G>A
AA Mutation p.Ala221Thr(p.A221T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000290399
Start 36741819:36741819(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747018347
CDS Mutation c.953G>A
AA Mutation p.Arg318His(p.R318H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000290399
Start 36743432:36743432(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1044C>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000290399
Start 36723074:36723074(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.487C>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000290399
Start 36745045:36745045(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1489delC
AA Mutation p.Leu497Ter(p.L497*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript