ClinVar Miner

List of variants in gene CLN3 reported as uncertain significance for not provided

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Gene type:
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Total variants: 64
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HGVS dbSNP
NM_000086.2(CLN3):c.-1G>T rs201274333
NM_000086.2(CLN3):c.1012C>T (p.Arg338Cys) rs776725094
NM_000086.2(CLN3):c.1028G>A (p.Arg343His) rs771305783
NM_000086.2(CLN3):c.1033A>T (p.Thr345Ser) rs150986176
NM_000086.2(CLN3):c.1086C>G (p.Asp362Glu) rs376907245
NM_000086.2(CLN3):c.1087G>A (p.Val363Met) rs370963882
NM_000086.2(CLN3):c.1117C>G (p.Leu373Val) rs752700529
NM_000086.2(CLN3):c.1120G>A (p.Val374Ile) rs759049027
NM_000086.2(CLN3):c.1163C>T (p.Ala388Val) rs148514847
NM_000086.2(CLN3):c.1168G>A (p.Val390Met) rs777383109
NM_000086.2(CLN3):c.1198-5C>T rs764999720
NM_000086.2(CLN3):c.1210C>T (p.His404Tyr) rs146610181
NM_000086.2(CLN3):c.1225A>G (p.Met409Val) rs776443981
NM_000086.2(CLN3):c.1230G>A (p.Ala410=) rs201206239
NM_000086.2(CLN3):c.1234A>G (p.Thr412Ala) rs1064795206
NM_000086.2(CLN3):c.1240A>G (p.Ile414Val)
NM_000086.2(CLN3):c.125+3G>A rs775577824
NM_000086.2(CLN3):c.1262C>T (p.Ser421Phe) rs778225078
NM_000086.2(CLN3):c.1285C>T (p.Pro429Ser) rs1433950864
NM_000086.2(CLN3):c.1309C>T (p.Leu437Phe) rs1085307617
NM_000086.2(CLN3):c.152C>T (p.Ser51Phe) rs780151271
NM_000086.2(CLN3):c.206C>T (p.Ser69Leu) rs769840061
NM_000086.2(CLN3):c.239C>T (p.Thr80Met) rs775999656
NM_000086.2(CLN3):c.242C>T (p.Pro81Leu) rs137906617
NM_000086.2(CLN3):c.250C>A (p.His84Asn) rs201329358
NM_000086.2(CLN3):c.266G>A (p.Arg89Gln) rs766287694
NM_000086.2(CLN3):c.270T>G (p.Phe90Leu) rs145520962
NM_000086.2(CLN3):c.308C>T (p.Ala103Val) rs760039703
NM_000086.2(CLN3):c.32T>C (p.Phe11Ser) rs752205710
NM_000086.2(CLN3):c.361C>G (p.Leu121Val) rs752282954
NM_000086.2(CLN3):c.380G>A (p.Arg127Gln) rs780776829
NM_000086.2(CLN3):c.388G>A (p.Val130Ile) rs764261700
NM_000086.2(CLN3):c.392G>A (p.Ser131Asn) rs144770450
NM_000086.2(CLN3):c.393T>C (p.Ser131=) rs794727850
NM_000086.2(CLN3):c.399T>C (p.Ile133=) rs775739498
NM_000086.2(CLN3):c.418G>A (p.Val140Ile) rs373034150
NM_000086.2(CLN3):c.461-3C>A rs181995380
NM_000086.2(CLN3):c.461-3C>G rs181995380
NM_000086.2(CLN3):c.472G>A (p.Ala158Thr) rs386833723
NM_000086.2(CLN3):c.49G>A (p.Glu17Lys) rs386833726
NM_000086.2(CLN3):c.537C>G (p.Ala179=) rs147667964
NM_000086.2(CLN3):c.575G>A (p.Gly192Glu) rs386833733
NM_000086.2(CLN3):c.586G>T (p.Ala196Ser) rs796052339
NM_000086.2(CLN3):c.616G>A (p.Gly206Ser) rs370603922
NM_000086.2(CLN3):c.649C>A (p.Leu217Met) rs150913606
NM_000086.2(CLN3):c.665T>A (p.Leu222Gln) rs781613318
NM_000086.2(CLN3):c.676A>G (p.Ser226Gly) rs1555468695
NM_000086.2(CLN3):c.707C>T (p.Ala236Val) rs754906598
NM_000086.2(CLN3):c.734_736del (p.Ala245del) rs776966610
NM_000086.2(CLN3):c.754C>T (p.Pro252Ser) rs769104531
NM_000086.2(CLN3):c.764G>A (p.Arg255Lys) rs1064795604
NM_000086.2(CLN3):c.767C>T (p.Thr256Ile) rs1064796298
NM_000086.2(CLN3):c.769G>A (p.Glu257Lys) rs771303379
NM_000086.2(CLN3):c.771G>C (p.Glu257Asp) rs73533466
NM_000086.2(CLN3):c.776C>T (p.Pro259Leu) rs137858807
NM_000086.2(CLN3):c.790+3A>C rs386833738
NM_000086.2(CLN3):c.814C>T (p.Arg272Trp) rs113041302
NM_000086.2(CLN3):c.831G>A (p.Val277=) rs1142183
NM_000086.2(CLN3):c.849G>T (p.Trp283Cys) rs1064795226
NM_000086.2(CLN3):c.859C>T (p.Pro287Ser) rs796052341
NM_000086.2(CLN3):c.868G>T (p.Val290Leu) rs369008702
NM_000086.2(CLN3):c.87C>A (p.Asp29Glu) rs1131691496
NM_000086.2(CLN3):c.938T>C (p.Leu313Pro) rs141816714
NM_000086.2(CLN3):c.976T>C (p.Tyr326His) rs796052337

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