Primary Site >> Liver Cancer

Gene >> SASH1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367467
Start 148525315:148525315(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1234G>C
AA Mutation p.Asp412His(p.D412H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367467
Start 148534782:148534782(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1976A>G
AA Mutation p.Tyr659Cys(p.Y659C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000367467
Start 148525325:148525325(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1244A>G
AA Mutation p.Asn415Ser(p.N415S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000367467
Start 148527474:148527474(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1306T>C
AA Mutation p.Tyr436His(p.Y436H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000367467
Start 148546100:148546100(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3434T>A
AA Mutation p.Met1145Lys(p.M1145K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000367467
Start 148519866:148519866(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1182G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000367467
Start 148543678:148543678(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2210-2A>T
Mutation Classification Splice_Site
Feature Type Transcript