Primary Site >> Liver Cancer

Gene >> DLG5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000372391
Start 77841928:77841928(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1390A>G
AA Mutation p.Thr464Ala(p.T464A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000372391
Start 77794089:77794089(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5575G>A
AA Mutation p.Asp1859Asn(p.D1859N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000372391
Start 77796571:77796571(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775531975
CDS Mutation c.5188C>T
AA Mutation p.Arg1730Trp(p.R1730W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000372391
Start 77817783:77817783(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3778C>G
AA Mutation p.Arg1260Gly(p.R1260G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000372391
Start 77821338:77821338(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3146G>T
AA Mutation p.Ser1049Ile(p.S1049I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000372391
Start 77809679:77809679(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4515C>T
Mutation Classification Silent
Feature Type Transcript