Primary Site >> Liver Cancer

Gene >> KMT2C

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262189
Start 152152875:152152875(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745808781
CDS Mutation c.12356C>T
AA Mutation p.Pro4119Leu(p.P4119L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262189
Start 152145280:152145280(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.14047G>C
AA Mutation p.Ala4683Pro(p.A4683P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262189
Start 152163609:152163609(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778241763
CDS Mutation c.9968A>C
AA Mutation p.His3323Pro(p.H3323P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262189
Start 152176443:152176443(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9010C>G
AA Mutation p.Leu3004Val(p.L3004V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262189
Start 152176926:152176926(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8527G>A
AA Mutation p.Asp2843Asn(p.D2843N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000262189
Start 152248064:152248064(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2370C>A
AA Mutation p.Asp790Glu(p.D790E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000262189
Start 152435762:152435762(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.25G>A
AA Mutation p.Val9Met(p.V9M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000262189
Start 152181850:152181850(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6010A>T
AA Mutation p.Ser2004Cys(p.S2004C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000262189
Start 152176507:152176507(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760077828
CDS Mutation c.8946T>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000262189
Start 152163326:152163326(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10251G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000262189
Start 152230007:152230007(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2892delC
AA Mutation p.Ser965ValfsTer66(p.S965Vfs*66)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000262189
Start 152187403:152187403(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4867G>T
AA Mutation p.Glu1623Ter(p.E1623*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence stop_lost
Transcription ID ENST00000262189
Start 152136833:152136833(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.14735G>T
AA Mutation p.Ter4912LeuextTer36(p.*4912Lext*36)
Mutation Classification Nonstop_Mutation
Feature Type Transcript