List of variants in gene LYST reported as likely benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_000081.4(LYST):c.5518T>G (p.Ser1840Ala)	rs115330112	0.00485
NM_000081.4(LYST):c.6482A>C (p.Glu2161Ala)	rs147756847	0.00416
NM_000081.4(LYST):c.5223T>C (p.Leu1741=)	rs7530527	0.00277
NM_000081.4(LYST):c.8487C>T (p.Ile2829=)	rs144597913	0.00126
NM_000081.4(LYST):c.4548C>T (p.Ser1516=)	rs116551057	0.00108
NM_000081.4(LYST):c.7506A>G (p.Gln2502=)	rs140434436	0.00106
NM_000081.4(LYST):c.6588A>G (p.Gly2196=)	rs34423788	0.00093
NM_000081.4(LYST):c.2769A>C (p.Ser923=)	rs112739986	0.00086
NM_000081.4(LYST):c.3507C>T (p.Leu1169=)	rs74861744	0.00083
NM_000081.4(LYST):c.2363+10dup	rs760632806	0.00058
NM_000081.4(LYST):c.143A>G (p.His48Arg)	rs200132460	0.00046
NM_000081.4(LYST):c.2946T>C (p.Tyr982=)	rs145892183	0.00034
NM_000081.4(LYST):c.2313G>A (p.Gln771=)	rs147220685	0.00031
NM_000081.4(LYST):c.3898A>G (p.Ile1300Val)	rs199855658	0.00021
NM_000081.4(LYST):c.4006+8G>A	rs369153654	0.00021
NM_000081.4(LYST):c.6432A>G (p.Ser2144=)	rs145080654	0.00011
NM_000081.4(LYST):c.3030A>G (p.Gly1010=)	rs751511204	0.00006
NM_000081.4(LYST):c.6258G>A (p.Glu2086=)	rs771882274	0.00006
NM_000081.4(LYST):c.8607A>G (p.Gln2869=)	rs369484787	0.00004
NM_000081.4(LYST):c.9804A>G (p.Pro3268=)	rs368740409	0.00004
NM_000081.4(LYST):c.3177T>C (p.Ala1059=)	rs371576746	0.00003
NM_000081.4(LYST):c.2757G>A (p.Ser919=)	rs753541871	0.00002
NM_000081.4(LYST):c.9834T>C (p.Thr3278=)	rs901343967	0.00002
NM_000081.4(LYST):c.11085C>T (p.Leu3695=)	rs767062870	0.00001
NM_000081.4(LYST):c.5037T>C (p.Gly1679=)	rs753293453	0.00001
NM_000081.4(LYST):c.9045-4A>G	rs769310836	0.00001
NM_000081.4(LYST):c.11268-5del	rs36014994
NM_000081.4(LYST):c.5922+10A>G	rs375422713
NM_000081.4(LYST):c.6570C>T (p.Val2190=)	rs1572170906
NM_000081.4(LYST):c.8358+7A>T	rs752173624

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