List of variants in gene CSTB reported as not provided for Unverricht-Lundborg syndrome

Minimum submission review status:		Collection method:
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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000100.4(CSTB):c.67-1G>C	rs147484110	0.00027
NM_000100.4(CSTB):c.202C>T (p.Arg68Ter)	rs74315442	0.00002
NM_000100.4(CSTB):c.125C>A (p.Ser42Ter)	rs386833439	0.00001
NM_000100.4(CSTB):c.136C>T (p.Gln46Ter)	rs545986367	0.00001
NM_000100.4(CSTB):c.149G>A (p.Gly50Glu)	rs312262708	0.00001
NM_000100.4(CSTB):c.168+2_168+19del	rs312262707
NM_000100.4(CSTB):c.168+2_168+21delinsAA	rs864309482
NM_000100.4(CSTB):c.168G>A (p.Lys56=)	rs386833440
NM_000100.4(CSTB):c.169-2A>G	rs386833441
NM_000100.4(CSTB):c.212A>C (p.Gln71Pro)	rs121909346
NM_000100.4(CSTB):c.218_219del (p.Leu73fs)	rs796943858

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