Primary Site >> Liver Cancer

Gene >> CHL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397491
Start 383863:383863(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2176A>G
AA Mutation p.Lys726Glu(p.K726E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397491
Start 401676:401676(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3388G>A
AA Mutation p.Asp1130Asn(p.D1130N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000397491
Start 399102:399102(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3291A>T
AA Mutation p.Leu1097Phe(p.L1097F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000397491
Start 366093:366093(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1681A>G
AA Mutation p.Ile561Val(p.I561V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000397491
Start 328274:328274(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.305A>T
AA Mutation p.His102Leu(p.H102L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000397491
Start 382228:382228(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1878G>T
AA Mutation p.Arg626Ser(p.R626S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000397491
Start 319846:319846(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.70G>T
AA Mutation p.Ala24Ser(p.A24S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000397491
Start 341974:341974(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.571G>T
AA Mutation p.Ala191Ser(p.A191S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000397491
Start 361764:361764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1324T>C
AA Mutation p.Phe442Leu(p.F442L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000397491
Start 398245:398245(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3065T>C
AA Mutation p.Ile1022Thr(p.I1022T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000397491
Start 389284:389284(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2232C>G
Mutation Classification Silent
Feature Type Transcript