Primary Site >> Liver Cancer

Gene >> SETD2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000409792
Start 47088127:47088127(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5263C>G
AA Mutation p.Leu1755Val(p.L1755V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000409792
Start 47057431:47057431(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6353C>T
AA Mutation p.Thr2118Ile(p.T2118I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000409792
Start 47124316:47124316(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.320C>T
AA Mutation p.Pro107Leu(p.P107L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000409792
Start 47120905:47120905(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768083138
CDS Mutation c.3731C>T
AA Mutation p.Pro1244Leu(p.P1244L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000409792
Start 47046618:47046618(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6967T>G
AA Mutation p.Tyr2323Asp(p.Y2323D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000409792
Start 47121569:47121569(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3067A>G
AA Mutation p.Ser1023Gly(p.S1023G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000409792
Start 47114003:47114003(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4588T>A
AA Mutation p.Ser1530Thr(p.S1530T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000409792
Start 47123735:47123735(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.901A>T
AA Mutation p.Ser301Cys(p.S301C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000409792
Start 47123239:47123239(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1397A>G
AA Mutation p.Lys466Arg(p.K466R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000409792
Start 47056881:47056881(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774810866
CDS Mutation c.6903A>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000409792
Start 47120376:47120376(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4260G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000409792
Start 47120571:47120571(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4065A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000409792
Start 47121858:47121858(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2778delA
AA Mutation p.Glu927LysfsTer3(p.E927Kfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000409792
Start 47120260:47120261(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4375_4376insAATGG
AA Mutation p.Arg1459GlnfsTer26(p.R1459Qfs*26)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 15
Mutation Consequence splice_donor_variant
Transcription ID ENST00000409792
Start 47120180:47120180(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4454+2T>G
Mutation Classification Splice_Site
Feature Type Transcript
ID 16
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000409792
Start 47042701:47042701(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7099-1G>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 17
Mutation Consequence splice_donor_variant
Transcription ID ENST00000409792
Start 47113875:47113875(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4715+1G>A
Mutation Classification Splice_Site
Feature Type Transcript