Mutation

Primary Site >> Liver Cancer

Gene >> ARID1A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324856
Start	26780158:26780158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6260G>A
AA Mutation	p.Gly2087Glu(p.G2087E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324856
Start	26780101:26780101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6203C>G
AA Mutation	p.Ser2068Trp(p.S2068W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324856
Start	26767881:26767881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3080A>G
AA Mutation	p.Tyr1027Cys(p.Y1027C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324856
Start	26696809:26696809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406C>A
AA Mutation	p.Pro136Thr(p.P136T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324856
Start	26774651:26774651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4424A>C
AA Mutation	p.Asn1475Thr(p.N1475T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324856
Start	26780538:26780538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6640A>T
AA Mutation	p.Ser2214Cys(p.S2214C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324856
Start	26767803:26767803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3002C>G
AA Mutation	p.Ser1001Cys(p.S1001C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324856
Start	26775623:26775623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5040C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324856
Start	26763199:26763199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149901342
CDS Mutation	c.2646G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26696897:26696897(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.494delC
AA Mutation	p.Ala165GlyfsTer67(p.A165Gfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26696727:26696731(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.324_328delCCCTA
AA Mutation	p.Pro109AlafsTer6(p.P109Afs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26775643:26775643(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5060delC
AA Mutation	p.Ala1687AspfsTer2(p.A1687Dfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26771309:26771318(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3389_3398delTCCAGCCTCC
AA Mutation	p.Ile1130ThrfsTer28(p.I1130Tfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26779685:26779685(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5788delT
AA Mutation	p.Ser1930GlnfsTer26(p.S1930Qfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26761403:26761407(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2181_2185delGCCAC
AA Mutation	p.Pro728GlnfsTer87(p.P728Qfs*87)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000324856
Start	26772517:26772517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3424C>T
AA Mutation	p.Gln1142Ter(p.Q1142*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000324856
Start	26774722:26774722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4495C>T
AA Mutation	p.Gln1499Ter(p.Q1499*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000324856
Start	26774851:26774851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4624G>T
AA Mutation	p.Glu1542Ter(p.E1542*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000324856
Start	26771305:26771305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3385A>T
AA Mutation	p.Lys1129Ter(p.K1129*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26779090:26779091(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5195dupA
AA Mutation	p.Glu1733GlyfsTer3(p.E1733Gfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26779808:26779809(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5915_5919dupACTGG
AA Mutation	p.Gln1974ThrfsTer43(p.Q1974Tfs*43)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26780593:26780594(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6697_6698dupCG
AA Mutation	p.Ala2234GlyfsTer34(p.A2234Gfs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26780014:26780015(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6116_6117insT
AA Mutation	p.Gln2039HisfsTer60(p.Q2039Hfs*60)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26780402:26780403(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6504_6505insT
AA Mutation	p.Val2169CysfsTer56(p.V2169Cfs*56)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26731210:26731211(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1411dupT
AA Mutation	p.Tyr471LeufsTer152(p.Y471Lfs*152)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	26
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000324856
Start	26775575:26775575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4994-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	27
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000324856
Start	26775625:26775648(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5042_5065delTGGCAGAGAGCACATGGGCATTAG
AA Mutation	p.Leu1681_Asp1689delinsHis(p.L1681_D1689delinsH)
Mutation Classification	In_Frame_Del
Feature Type	Transcript