Primary Site >> Liver Cancer

Gene >> SCEL

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000349847
Start 77637193:77637193(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1837A>T
AA Mutation p.Arg613Trp(p.R613W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000349847
Start 77589205:77589205(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.607C>A
AA Mutation p.Gln203Lys(p.Q203K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000349847
Start 77559822:77559822(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.180G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000349847
Start 77627977:77627977(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1659A>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000349847
Start 77640782:77640782(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1945A>T
AA Mutation p.Lys649Ter(p.K649*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript