ClinVar Miner

List of variants in gene TARDBP reported as likely benign for Amyotrophic lateral sclerosis type 10; FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, TARDBP-RELATED

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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_007375.4(TARDBP):c.239-15G>A rs200066188 0.00034
NM_007375.4(TARDBP):c.945G>A (p.Ala315=) rs145364830 0.00010
NM_007375.4(TARDBP):c.975C>T (p.Ala325=) rs777072801 0.00009
NM_007375.4(TARDBP):c.36C>T (p.Asn12=) rs565091566 0.00008
NM_007375.4(TARDBP):c.1101C>T (p.Phe367=) rs377531374 0.00007
NM_007375.4(TARDBP):c.669C>G (p.Pro223=) rs149517613 0.00007
NM_007375.4(TARDBP):c.330T>G (p.Gly110=) rs199804130 0.00005
NM_007375.4(TARDBP):c.642C>T (p.Tyr214=) rs138201492 0.00005
NM_007375.4(TARDBP):c.714+17C>T rs374054081 0.00005
NM_007375.4(TARDBP):c.87C>T (p.Ser29=) rs201693535 0.00005
NM_007375.4(TARDBP):c.1122T>C (p.Tyr374=) rs147795017 0.00004
NM_007375.4(TARDBP):c.57A>G (p.Pro19=) rs532319219 0.00004
NM_007375.4(TARDBP):c.720G>A (p.Ala240=) rs765175133 0.00004
NM_007375.4(TARDBP):c.239-11G>A rs200694980 0.00003
NM_007375.4(TARDBP):c.312C>T (p.Ser104=) rs774307145 0.00003
NM_007375.4(TARDBP):c.403-14A>G rs370601916 0.00003
NM_007375.4(TARDBP):c.403-5T>C rs372872536 0.00003
NM_007375.4(TARDBP):c.714+18G>A rs772366877 0.00003
NM_007375.4(TARDBP):c.900A>G (p.Gly300=) rs146402671 0.00003
NM_007375.4(TARDBP):c.1056T>C (p.Asn352=) rs561479675 0.00002
NM_007375.4(TARDBP):c.239-12C>T rs753108059 0.00002
NM_007375.4(TARDBP):c.544-15T>C rs753859058 0.00002
NM_007375.4(TARDBP):c.1179G>A (p.Ser393=) rs543149287 0.00001
NM_007375.4(TARDBP):c.12T>C (p.Tyr4=) rs1179641429 0.00001
NM_007375.4(TARDBP):c.162C>T (p.Val54=) rs751073315 0.00001
NM_007375.4(TARDBP):c.189C>T (p.Ala63=) rs1399738284 0.00001
NM_007375.4(TARDBP):c.273A>G (p.Ser91=) rs369009972 0.00001
NM_007375.4(TARDBP):c.360G>A (p.Leu120=) rs1333754120 0.00001
NM_007375.4(TARDBP):c.402+19A>G rs200818944 0.00001
NM_007375.4(TARDBP):c.411A>G (p.Lys137=) rs766028449 0.00001
NM_007375.4(TARDBP):c.465T>C (p.Tyr155=) rs1207947256 0.00001
NM_007375.4(TARDBP):c.543+20G>T rs2521310503 0.00001
NM_007375.4(TARDBP):c.543+9G>A rs370342366 0.00001
NM_007375.4(TARDBP):c.622C>A (p.Arg208=) rs1643615862 0.00001
NM_007375.4(TARDBP):c.715-11A>G rs767002230 0.00001
NM_007375.4(TARDBP):c.780C>T (p.Ala260=) rs945279656 0.00001
NM_007375.4(TARDBP):c.930G>A (p.Gly310=) rs552576600 0.00001
NM_007375.4(TARDBP):c.963C>T (p.Ala321=) rs547979470 0.00001
NM_007375.4(TARDBP):c.990A>G (p.Leu330=) rs1469816236 0.00001
NM_007375.4(TARDBP):c.1005T>A (p.Gly335=) rs998379166
NM_007375.4(TARDBP):c.1050G>C (p.Ser350=)
NM_007375.4(TARDBP):c.111G>A (p.Gly37=) rs1553158651
NM_007375.4(TARDBP):c.114G>A (p.Ala38=) rs535276506
NM_007375.4(TARDBP):c.1173A>G (p.Ala391=) rs2521343663
NM_007375.4(TARDBP):c.238+16G>T rs373450963
NM_007375.4(TARDBP):c.348C>T (p.Thr116=)
NM_007375.4(TARDBP):c.495A>G (p.Arg165=) rs2521309907
NM_007375.4(TARDBP):c.543+15G>A rs749471636
NM_007375.4(TARDBP):c.543+16C>G rs1643580863
NM_007375.4(TARDBP):c.544-6G>C rs2100852266
NM_007375.4(TARDBP):c.609T>G (p.Thr203=) rs2521324563
NM_007375.4(TARDBP):c.636T>G (p.Ser212=) rs2521324781
NM_007375.4(TARDBP):c.699A>G (p.Thr233=) rs745343269
NM_007375.4(TARDBP):c.715-18A>G rs2521340219
NM_007375.4(TARDBP):c.774C>G (p.Ser258=) rs763180944
NM_007375.4(TARDBP):c.909A>G (p.Gln303=) rs1375684772
NM_007375.4(TARDBP):c.939T>C (p.Phe313=) rs2100856402

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