ClinVar Miner

List of variants in gene LYST reported by PreventionGenetics

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Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP
NM_000081.3(LYST):c.-5C>T rs141317482
NM_000081.3(LYST):c.10110T>C (p.Ala3370=) rs886038227
NM_000081.3(LYST):c.10374+33A>G rs17615059
NM_000081.3(LYST):c.10564+43G>A rs7541057
NM_000081.3(LYST):c.11039-24C>T rs12088737
NM_000081.3(LYST):c.1251A>G (p.Gln417=) rs1063128
NM_000081.3(LYST):c.153A>C (p.Gly51=) rs11464
NM_000081.3(LYST):c.1683A>G (p.Leu561=) rs3820553
NM_000081.3(LYST):c.1686G>C (p.Gln562His) rs77091385
NM_000081.3(LYST):c.2316C>T (p.Asp772=) rs16832868
NM_000081.3(LYST):c.2355T>C (p.Leu785=) rs3768066
NM_000081.3(LYST):c.3050G>A (p.Ser1017Asn) rs10465613
NM_000081.3(LYST):c.3359G>T (p.Ser1120Ile) rs143223086
NM_000081.3(LYST):c.3394-14T>C rs372892911
NM_000081.3(LYST):c.3713-26G>A rs9803890
NM_000081.3(LYST):c.3989A>C (p.Asp1330Ala) rs74641549
NM_000081.3(LYST):c.4392C>T (p.Asn1464=) rs11583387
NM_000081.3(LYST):c.4863-19T>C rs150288597
NM_000081.3(LYST):c.4956A>G (p.Leu1652=) rs6696123
NM_000081.3(LYST):c.5023+41C>T rs72763416
NM_000081.3(LYST):c.5024-43T>G rs7543060
NM_000081.3(LYST):c.5291G>C (p.Gly1764Ala) rs35413645
NM_000081.3(LYST):c.5373G>A (p.Lys1791=) rs2273584
NM_000081.3(LYST):c.5518T>G (p.Ser1840Ala) rs115330112
NM_000081.3(LYST):c.574T>G (p.Leu192Val) rs7524261
NM_000081.3(LYST):c.5847G>C (p.Gln1949His) rs6665568
NM_000081.3(LYST):c.5923-19G>T rs141197189
NM_000081.3(LYST):c.6122-13delA rs201404906
NM_000081.3(LYST):c.6482A>C (p.Glu2161Ala) rs147756847
NM_000081.3(LYST):c.6630A>G (p.Glu2210=) rs34466404
NM_000081.3(LYST):c.6782G>A (p.Arg2261His) rs147791378
NM_000081.3(LYST):c.6812A>G (p.Asp2271Gly) rs112601869
NM_000081.3(LYST):c.6881+44A>G rs3738519
NM_000081.3(LYST):c.6900G>A (p.Leu2300=) rs10926586
NM_000081.3(LYST):c.7059+7G>A rs111764031
NM_000081.3(LYST):c.7137A>C (p.Leu2379=) rs61738992
NM_000081.3(LYST):c.7506A>G (p.Gln2502=) rs140434436
NM_000081.3(LYST):c.7793T>A (p.Phe2598Tyr) rs34642241
NM_000081.3(LYST):c.7857T>C (p.His2619=) rs34160788
NM_000081.3(LYST):c.8411G>A (p.Gly2804Asp) rs35333195
NM_000081.3(LYST):c.9C>T (p.Thr3=) rs33998267

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