Primary Site >> Liver Cancer

Gene >> EMILIN2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000254528
Start 2909796:2909796(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2801G>T
AA Mutation p.Gly934Val(p.G934V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000254528
Start 2885056:2885056(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773279293
CDS Mutation c.350A>G
AA Mutation p.Asp117Gly(p.D117G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000254528
Start 2890916:2890916(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.789G>T
AA Mutation p.Lys263Asn(p.K263N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000254528
Start 2891714:2891714(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1587G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000254528
Start 2891531:2891531(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1404C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000254528
Start 2885114:2885114(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.408T>A
Mutation Classification Silent
Feature Type Transcript