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

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000081.4(LYST):c.5024-43T>G	rs7543060	0.04336
NM_000081.4(LYST):c.3989A>C (p.Asp1330Ala)	rs74641549	0.04030
NM_000081.4(LYST):c.3713-26G>A	rs9803890	0.04021
NM_000081.4(LYST):c.5945C>T (p.Thr1982Ile)	rs146591126	0.00669
NM_000081.4(LYST):c.7059+7G>A	rs111764031	0.00582
NM_000081.4(LYST):c.6812A>G (p.Asp2271Gly)	rs112601869	0.00580
NM_000081.4(LYST):c.10800+4G>T	rs41308172	0.00441
NM_000081.4(LYST):c.6482A>C (p.Glu2161Ala)	rs147756847	0.00416
NM_000081.4(LYST):c.1686G>C (p.Gln562His)	rs77091385	0.00394
NM_000081.4(LYST):c.7870C>T (p.Arg2624Trp)	rs150306354	0.00280
NM_000081.4(LYST):c.5223T>C (p.Leu1741=)	rs7530527	0.00277
NM_000081.4(LYST):c.597C>G (p.Asp199Glu)	rs112127610	0.00238
NM_000081.4(LYST):c.6710A>C (p.Gln2237Pro)	rs138443479	0.00148
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.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.11086G>A (p.Val3696Ile)	rs147221131	0.00052
NM_000081.4(LYST):c.4863-4G>A	rs201382097	0.00032
NM_000081.4(LYST):c.3394-14T>C	rs372892911	0.00029
NM_000081.4(LYST):c.368A>G (p.His123Arg)	rs3768067	0.00027
NM_000081.4(LYST):c.6487G>A (p.Ala2163Thr)	rs201513511	0.00026
NM_000081.4(LYST):c.7368T>C (p.Asn2456=)	rs199631995	0.00026
NM_000081.4(LYST):c.281C>T (p.Thr94Ile)	rs777389303	0.00009
NM_000081.4(LYST):c.2553T>C (p.Ser851=)	rs769690916	0.00001
NM_000081.4(LYST):c.463G>C (p.Val155Leu)	rs769942827	0.00001
NM_000081.4(LYST):c.7761A>G (p.Gln2587=)	rs139917441	0.00001
NM_000081.4(LYST):c.5461-3dup	rs557545474
NM_000081.4(LYST):c.8612+13A>G
NM_000081.4(LYST):c.8801+14G>T

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