Primary Site >> Liver Cancer

Gene >> ARID2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45852625:45852625(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4502C>T
AA Mutation p.Ser1501Phe(p.S1501F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45836893:45836893(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.925A>T
AA Mutation p.Asn309Tyr(p.N309Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45852368:45852368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4245T>G
AA Mutation p.Ile1415Met(p.I1415M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45850839:45850839(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2716G>C
AA Mutation p.Val906Leu(p.V906L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45836939:45836939(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.971T>G
AA Mutation p.Phe324Cys(p.F324C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000334344
Start 45860949:45860949(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4922A>C
AA Mutation p.Lys1641Thr(p.K1641T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45850500:45850500(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2377C>A
AA Mutation p.Gln793Lys(p.Q793K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000334344
Start 45839454:45839454(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370535448
CDS Mutation c.1456A>G
AA Mutation p.Ile486Val(p.I486V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000334344
Start 45837520:45837520(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1143T>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45730119:45730119(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.170delT
AA Mutation p.Leu57Ter(p.L57*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45852716:45852716(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4595delA
AA Mutation p.Asn1532IlefsTer3(p.N1532Ifs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45821464:45821464(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.683delA
AA Mutation p.Lys228ArgfsTer64(p.K228Rfs*64)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45852581:45852593(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4460_4472delCCGACTCAGGATC
AA Mutation p.Pro1487GlnfsTer25(p.P1487Qfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45850563:45850564(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2441_2442delCA
AA Mutation p.Thr814SerfsTer26(p.T814Sfs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45891858:45891858(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5001T>A
AA Mutation p.Cys1667Ter(p.C1667*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45850158:45850158(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2035C>T
AA Mutation p.Gln679Ter(p.Q679*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45837406:45837406(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1109T>G
AA Mutation p.Leu370Ter(p.L370*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45811433:45811433(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.300C>G
AA Mutation p.Tyr100Ter(p.Y100*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45851940:45851940(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3817C>T
AA Mutation p.Arg1273Ter(p.R1273*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence stop_gained
Transcription ID ENST00000334344
Start 45836765:45836765(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.797G>A
AA Mutation p.Trp266Ter(p.W266*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence frameshift_variant
Transcription ID ENST00000334344
Start 45850666:45850667(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2544dupA
AA Mutation p.Ala849SerfsTer102(p.A849Sfs*102)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 22
Mutation Consequence splice_donor_variant
Transcription ID ENST00000334344
Start 45852897:45852897(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4773+1G>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 23
Mutation Consequence splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000334344
Start 45836735:45836762(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.773-3_797delTAGAAGGTACATCAGGAGAATGGATTTG
Mutation Classification Splice_Site
Feature Type Transcript
ID 24
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000334344
Start 45860799:45860799(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4774-2A>G
Mutation Classification Splice_Site
Feature Type Transcript