Primary Site >> Liver Cancer

Gene >> SIM2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000290399
Start 36743469:36743469(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745663760
CDS Mutation c.1081T>C
AA Mutation p.Ser361Pro(p.S361P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000290399
Start 36726294:36726294(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.719T>C
AA Mutation p.Leu240Pro(p.L240P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000290399
Start 36744741:36744741(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1181T>C
AA Mutation p.Phe394Ser(p.F394S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000290399
Start 36726219:36726219(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.644A>G
AA Mutation p.Gln215Arg(p.Q215R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000290399
Start 36745027:36745027(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1467C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000290399
Start 36723109:36723109(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.522C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_donor_variant
Transcription ID ENST00000290399
Start 36743557:36743557(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1167+2T>C
Mutation Classification Splice_Site
Feature Type Transcript