List of variants in gene CLN3 reported as likely benign for Neuronal ceroid lipofuscinosis 3

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001042432.2(CLN3):c.1211A>G (p.His404Arg)	rs77595156	0.11421
NM_001042432.2(CLN3):c.*155A>C	rs113112766	0.00886
NM_001042432.2(CLN3):c.318C>T (p.Leu106=)	rs148248159	0.00115
NM_001042432.2(CLN3):c.831G>A (p.Val277=)	rs1142183	0.00045
NM_001042432.2(CLN3):c.1230G>A (p.Ala410=)	rs201206239	0.00040
NM_001042432.2(CLN3):c.677+8G>A	rs368568189	0.00015
NM_001042432.2(CLN3):c.615C>T (p.Ala205=)	rs145631076	0.00005
NM_001042432.2(CLN3):c.516C>T (p.Leu172=)	rs148846795	0.00004
NM_001042432.2(CLN3):c.240G>A (p.Thr80=)	rs373911322	0.00002
NM_001042432.2(CLN3):c.447G>T (p.Gly149=)	rs779918787	0.00002
NM_001042432.2(CLN3):c.309G>A (p.Ala103=)	rs774996613	0.00001
NM_001042432.2(CLN3):c.1210C>A (p.His404Asn)	rs146610181
NM_001042432.2(CLN3):c.223-8C>T	rs973448262
NM_001042432.2(CLN3):c.537C>G (p.Ala179=)	rs147667964
NM_001042432.2(CLN3):c.582G>T (p.Leu194=)	rs386833734
NM_001042432.2(CLN3):c.963-63_963-44dup	rs1555468153

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