Primary Site >> Liver Cancer

Gene >> TCHH

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368804
Start 152108245:152108245(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749152495
CDS Mutation c.4972G>A
AA Mutation p.Glu1658Lys(p.E1658K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368804
Start 152110875:152110875(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2342G>T
AA Mutation p.Arg781Leu(p.R781L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368804
Start 152111847:152111847(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1370G>T
AA Mutation p.Trp457Leu(p.W457L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368804
Start 152107878:152107878(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199599922
CDS Mutation c.5339G>T
AA Mutation p.Arg1780Leu(p.R1780L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368804
Start 152109828:152109828(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3389A>C
AA Mutation p.Lys1130Thr(p.K1130T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000368804
Start 152108766:152108766(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4451A>G
AA Mutation p.Asp1484Gly(p.D1484G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000368804
Start 152111004:152111004(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2213A>T
AA Mutation p.Lys738Met(p.K738M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000368804
Start 152108161:152108161(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5056C>T
AA Mutation p.Arg1686Cys(p.R1686C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000368804
Start 152111726:152111726(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1491C>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000368804
Start 152114042:152114042(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.39A>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000368804
Start 152111500:152111500(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1717G>T
AA Mutation p.Glu573Ter(p.E573*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence inframe_deletion
Transcription ID ENST00000368804
Start 152107772:152107843(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5374_5445delGAGTCTGACAGAAAATTCCGCGAGGAGGAACAGCTACGCCAGGAGAGGGAAGAACAGCAGCTGCGCCCCCAA
AA Mutation p.Glu1792_Gln1815del(p.E1792_Q1815del)
Mutation Classification In_Frame_Del
Feature Type Transcript
ID 13
Mutation Consequence inframe_deletion
Transcription ID ENST00000368804
Start 152109692:152109781(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3436_3525delGTGCAGCAGGAGGAAGAGCAGCTGCTGAGAGAGGAACCGGAGAAGAGAAGGCGCCAGGAGCTGGAGAGGCAATACCGCGAGGAAGAGGAG
AA Mutation p.Val1146_Glu1175del(p.V1146_E1175del)
Mutation Classification In_Frame_Del
Feature Type Transcript