ClinVar Miner

List of variants in gene LYST reported by Preventiongenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_000081.4(LYST):c.10564+43G>A rs7541057 0.55363
NM_000081.4(LYST):c.1251A>G (p.Gln417=) rs1063128 0.41864
NM_000081.4(LYST):c.1683A>G (p.Leu561=) rs3820553 0.41844
NM_000081.4(LYST):c.4956A>G (p.Leu1652=) rs6696123 0.41826
NM_000081.4(LYST):c.5373G>A (p.Lys1791=) rs2273584 0.41769
NM_000081.4(LYST):c.6881+44A>G rs3738519 0.30798
NM_000081.4(LYST):c.153A>C (p.Gly51=) rs11464 0.13219
NM_000081.4(LYST):c.2355T>C (p.Leu785=) rs3768066 0.10928
NM_000081.4(LYST):c.5023+41C>T rs72763416 0.10897
NM_000081.4(LYST):c.4392C>T (p.Asn1464=) rs11583387 0.09239
NM_000081.4(LYST):c.11039-24C>T rs12088737 0.08504
NM_000081.4(LYST):c.2316C>T (p.Asp772=) rs16832868 0.05899
NM_000081.4(LYST):c.5847G>C (p.Gln1949His) rs6665568 0.05891
NM_000081.4(LYST):c.6630A>G (p.Glu2210=) rs34466404 0.05877
NM_000081.4(LYST):c.574T>G (p.Leu192Val) rs7524261 0.04386
NM_000081.4(LYST):c.5024-43T>G rs7543060 0.04336
NM_000081.4(LYST):c.8411G>A (p.Gly2804Asp) rs35333195 0.04044
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.3050G>A (p.Ser1017Asn) rs10465613 0.03661
NM_000081.4(LYST):c.5923-19G>T rs141197189 0.03063
NM_000081.4(LYST):c.7857T>C (p.His2619=) rs34160788 0.02966
NM_000081.4(LYST):c.6900G>A (p.Leu2300=) rs10926586 0.02954
NM_000081.4(LYST):c.7137A>C (p.Leu2379=) rs61738992 0.02884
NM_000081.4(LYST):c.7793T>A (p.Phe2598Tyr) rs34642241 0.02388
NM_000081.4(LYST):c.10374+33A>G rs17615059 0.02070
NM_000081.4(LYST):c.9C>T (p.Thr3=) rs33998267 0.01172
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.5518T>G (p.Ser1840Ala) rs115330112 0.00485
NM_000081.4(LYST):c.-5C>T rs141317482 0.00475
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.4863-19T>C rs150288597 0.00393
NM_000081.4(LYST):c.5291G>C (p.Gly1764Ala) rs35413645 0.00350
NM_000081.4(LYST):c.3359G>T (p.Ser1120Ile) rs143223086 0.00302
NM_000081.4(LYST):c.7506A>G (p.Gln2502=) rs140434436 0.00106
NM_000081.4(LYST):c.8027G>T (p.Ser2676Ile) rs113209379 0.00086
NM_000081.4(LYST):c.10235G>A (p.Arg3412His) rs148409403 0.00073
NM_000081.4(LYST):c.6782G>A (p.Arg2261His) rs147791378 0.00031
NM_000081.4(LYST):c.3394-14T>C rs372892911 0.00029
NM_000081.4(LYST):c.5374A>G (p.Asn1792Asp) rs143696500 0.00010
NM_000081.4(LYST):c.6737T>G (p.Leu2246Arg) rs200231136 0.00004
NM_000081.4(LYST):c.10459C>T (p.Gln3487Ter)
NM_000081.4(LYST):c.10468G>A (p.Gly3490Arg)
NM_000081.4(LYST):c.1481C>T (p.Ser494Leu)
NM_000081.4(LYST):c.2058G>C (p.Leu686Phe)
NM_000081.4(LYST):c.2465C>T (p.Thr822Ile)
NM_000081.4(LYST):c.2720del (p.Leu907fs)
NM_000081.4(LYST):c.285T>G (p.Asp95Glu) rs747965676
NM_000081.4(LYST):c.3223G>A (p.Val1075Met)
NM_000081.4(LYST):c.3644T>C (p.Leu1215Ser)
NM_000081.4(LYST):c.4670A>G (p.Asn1557Ser)
NM_000081.4(LYST):c.6122-13del rs201404906
NM_000081.4(LYST):c.6454A>C (p.Ser2152Arg)
NM_000081.4(LYST):c.6791G>C (p.Ser2264Thr)
NM_000081.4(LYST):c.8623C>T (p.Arg2875Cys)
NM_000081.4(LYST):c.9319C>T (p.Arg3107Cys)
NM_000081.4(LYST):c.9541A>C (p.Asn3181His)

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