Primary Site >> Liver Cancer

Gene >> LOXL4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000260702
Start 98253736:98253736(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375427147
CDS Mutation c.1652G>A
AA Mutation p.Arg551His(p.R551H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000260702
Start 98253730:98253730(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1658T>A
AA Mutation p.Leu553His(p.L553H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000260702
Start 98262084:98262084(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377758453
CDS Mutation c.407G>A
AA Mutation p.Arg136His(p.R136H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000260702
Start 98257796:98257796(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs11189525
CDS Mutation c.1114C>A
AA Mutation p.Pro372Thr(p.P372T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000260702
Start 98257770:98257770(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771955268
CDS Mutation c.1140C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000260702
Start 98251683:98251683(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1971A>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence inframe_deletion
Transcription ID ENST00000260702
Start 98251618:98251638(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2016_2036delCACCTACCGGCATGACATTGA
AA Mutation p.Thr673_Asp679del(p.T673_D679del)
Mutation Classification In_Frame_Del
Feature Type Transcript