Primary Site >> Liver Cancer

Gene >> SLX4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3584827:3584827(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4681A>G
AA Mutation p.Thr1561Ala(p.T1561A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3591075:3591075(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2563T>G
AA Mutation p.Tyr855Asp(p.Y855D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3584808:3584808(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4700C>G
AA Mutation p.Ser1567Cys(p.S1567C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3608811:3608811(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.154A>G
AA Mutation p.Lys52Glu(p.K52E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3583141:3583141(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777602041
CDS Mutation c.5109G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3597562:3597562(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1500G>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3601152:3601152(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.990G>T
Mutation Classification Silent
Feature Type Transcript