Primary Site >> Liver Cancer

Gene >> KMT2B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35722668:35722668(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2672C>G
AA Mutation p.Pro891Arg(p.P891R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35725512:35725512(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3676C>T
AA Mutation p.His1226Tyr(p.H1226Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35725498:35725498(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3662G>T
AA Mutation p.Cys1221Phe(p.C1221F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35729216:35729216(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4837A>G
AA Mutation p.Ile1613Val(p.I1613V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35728134:35728134(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4534G>A
AA Mutation p.Asp1512Asn(p.D1512N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35720266:35720266(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs540162147
CDS Mutation c.919T>C
AA Mutation p.Phe307Leu(p.F307L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35737145:35737145(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7432C>A
AA Mutation p.Gln2478Lys(p.Q2478K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35723199:35723199(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2927A>G
AA Mutation p.Gln976Arg(p.Q976R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000420124
Start 35732091:35732091(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5621G>T
AA Mutation p.Arg1874Leu(p.R1874L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35733317:35733317(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6768A>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000420124
Start 35730116:35730116(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5067G>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000420124
Start 35732101:35732101(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5636delG
AA Mutation p.Gly1879ValfsTer16(p.G1879Vfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000420124
Start 35732060:35732060(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5590C>T
AA Mutation p.Arg1864Ter(p.R1864*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000420124
Start 35723998:35723998(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3325C>T
AA Mutation p.Arg1109Ter(p.R1109*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000420124
Start 35728149:35728149(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4549C>T
AA Mutation p.Arg1517Ter(p.R1517*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000420124
Start 35730764:35730764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5334C>A
AA Mutation p.Cys1778Ter(p.C1778*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence splice_donor_variant
Transcription ID ENST00000420124
Start 35738192:35738192(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7872+1G>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 18
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000420124
Start 35725219:35725219(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3529-1G>C
Mutation Classification Splice_Site
Feature Type Transcript