ClinVar Miner

List of variants in gene CLN3 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP
NM_000086.2(CLN3):c.-17G>A rs770428655
NM_000086.2(CLN3):c.-249A>C rs1555469548
NM_000086.2(CLN3):c.-274T>C rs1362294732
NM_000086.2(CLN3):c.-275C>G rs946396606
NM_000086.2(CLN3):c.-33C>A rs368494637
NM_000086.2(CLN3):c.-41C>A rs370217726
NM_000086.2(CLN3):c.-90G>A rs368542813
NM_000086.2(CLN3):c.1022G>A (p.Arg341His) rs201271341
NM_000086.2(CLN3):c.1056+8A>C rs991918245
NM_000086.2(CLN3):c.1057-11C>T rs189498501
NM_000086.2(CLN3):c.1135C>T (p.Leu379=) rs890026046
NM_000086.2(CLN3):c.1150C>T (p.Leu384=) rs1057521416
NM_000086.2(CLN3):c.1167C>T (p.Tyr389=) rs371025471
NM_000086.2(CLN3):c.1197+13C>A rs370103287
NM_000086.2(CLN3):c.1198-14C>G rs757911107
NM_000086.2(CLN3):c.1198-17G>A rs749612121
NM_000086.2(CLN3):c.1210C>A (p.His404Asn) rs146610181
NM_000086.2(CLN3):c.1211A>G (p.His404Arg) rs77595156
NM_000086.2(CLN3):c.1213C>A (p.Arg405=) rs139842473
NM_000086.2(CLN3):c.125+3G>A rs775577824
NM_000086.2(CLN3):c.180C>T (p.His60=) rs150120797
NM_000086.2(CLN3):c.207G>A (p.Ser69=) rs551476103
NM_000086.2(CLN3):c.222+9CT[2] rs1064794997
NM_000086.2(CLN3):c.240G>A (p.Thr80=) rs373911322
NM_000086.2(CLN3):c.243G>A (p.Pro81=) rs779165392
NM_000086.2(CLN3):c.288T>A (p.Ser96=) rs1555469051
NM_000086.2(CLN3):c.295-13T>A rs796052333
NM_000086.2(CLN3):c.295-17C>G rs375311626
NM_000086.2(CLN3):c.304C>T (p.Leu102=) rs1167562278
NM_000086.2(CLN3):c.309G>A (p.Ala103=) rs774996613
NM_000086.2(CLN3):c.313A>G (p.Ile105Val) rs11552531
NM_000086.2(CLN3):c.318C>T (p.Leu106=) rs148248159
NM_000086.2(CLN3):c.33T>C (p.Phe11=) rs1555469504
NM_000086.2(CLN3):c.375-19_375-4dup rs755313503
NM_000086.2(CLN3):c.447G>T (p.Gly149=) rs779918787
NM_000086.2(CLN3):c.47-11C>A rs561083322
NM_000086.2(CLN3):c.47-4C>T rs1555469480
NM_000086.2(CLN3):c.533+18G>A rs376160790
NM_000086.2(CLN3):c.534-18C>T rs1310342698
NM_000086.2(CLN3):c.615C>T (p.Ala205=) rs145631076
NM_000086.2(CLN3):c.677+19G>A rs367594758
NM_000086.2(CLN3):c.768C>T (p.Thr256=) rs145967477
NM_000086.2(CLN3):c.777G>A (p.Pro259=) rs751443804
NM_000086.2(CLN3):c.791-6C>T rs1057523421
NM_000086.2(CLN3):c.831G>A (p.Val277=) rs1142183
NM_000086.2(CLN3):c.837+12G>A rs763812265
NM_000086.2(CLN3):c.861C>T (p.Pro287=) rs1057524528
NM_000086.2(CLN3):c.870A>G (p.Val290=) rs1555468214
NM_000086.2(CLN3):c.882C>T (p.Ala294=) rs766972077
NM_000086.2(CLN3):c.963-16C>A rs200023908

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