ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 23
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NM_000086.2(CLN3):c.-80G>T rs796052334
NM_000086.2(CLN3):c.1197+13C>T rs370103287
NM_000086.2(CLN3):c.1197+8T>C rs587780895
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.1230G>A (p.Ala410=) rs201206239
NM_000086.2(CLN3):c.174C>T (p.Ala58=) rs138433617
NM_000086.2(CLN3):c.240G>A (p.Thr80=) rs373911322
NM_000086.2(CLN3):c.264A>C (p.Ser88=) rs751321507
NM_000086.2(CLN3):c.270T>C (p.Phe90=) rs145520962
NM_000086.2(CLN3):c.295-17C>T rs375311626
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.45G>A (p.Glu15=) rs201824641
NM_000086.2(CLN3):c.516C>T (p.Leu172=) rs148846795
NM_000086.2(CLN3):c.677+8G>A rs368568189
NM_000086.2(CLN3):c.678-18C>A rs370158185
NM_000086.2(CLN3):c.768C>T (p.Thr256=) rs145967477
NM_000086.2(CLN3):c.771G>A (p.Glu257=) rs73533466
NM_000086.2(CLN3):c.790+16C>A rs200731769
NM_000086.2(CLN3):c.831G>A (p.Val277=) rs1142183
NM_000086.2(CLN3):c.963-16C>G rs200023908
NM_000086.2(CLN3):c.975G>A (p.Leu325=) rs150174473

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