ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 126
Download table as spreadsheet
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.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.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.7870C>T (p.Arg2624Trp) rs150306354 0.00280
NM_000081.4(LYST):c.8913T>G (p.Asn2971Lys) rs34702903 0.00276
NM_000081.4(LYST):c.3683A>G (p.Asn1228Ser) rs145553827 0.00171
NM_000081.4(LYST):c.6710A>C (p.Gln2237Pro) rs138443479 0.00148
NM_000081.4(LYST):c.6632C>G (p.Pro2211Arg) rs138972355 0.00140
NM_000081.4(LYST):c.4337G>A (p.Arg1446Gln) rs111722949 0.00135
NM_000081.4(LYST):c.7506A>G (p.Gln2502=) rs140434436 0.00106
NM_000081.4(LYST):c.11382C>T (p.Phe3794=) rs111770759 0.00102
NM_000081.4(LYST):c.2769A>C (p.Ser923=) rs112739986 0.00086
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.4637C>T (p.Ala1546Val) rs142983846 0.00054
NM_000081.4(LYST):c.11086G>A (p.Val3696Ile) rs147221131 0.00052
NM_000081.4(LYST):c.692A>G (p.Gln231Arg) rs147433918 0.00043
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.595G>A (p.Asp199Asn) rs552391792 0.00018
NM_000081.4(LYST):c.2700A>G (p.Leu900=) rs111463684 0.00017
NM_000081.4(LYST):c.6291C>T (p.Ala2097=) rs199857997 0.00016
NM_000081.4(LYST):c.6388G>A (p.Asp2130Asn) rs148371004 0.00014
NM_000081.4(LYST):c.8151T>C (p.Ile2717=) rs201045270 0.00012
NM_000081.4(LYST):c.5374A>G (p.Asn1792Asp) rs143696500 0.00010
NM_000081.4(LYST):c.3834G>A (p.Leu1278=) rs148542548 0.00006
NM_000081.4(LYST):c.6258G>A (p.Glu2086=) rs771882274 0.00006
NM_000081.4(LYST):c.3465A>G (p.Gln1155=) rs142982293 0.00004
NM_000081.4(LYST):c.4705A>C (p.Asn1569His) rs767687843 0.00004
NM_000081.4(LYST):c.6737T>G (p.Leu2246Arg) rs200231136 0.00004
NM_000081.4(LYST):c.4566A>C (p.Ala1522=) rs142344106 0.00003
NM_000081.4(LYST):c.8259G>A (p.Ser2753=) rs116017878 0.00003
NM_000081.4(LYST):c.8497G>A (p.Ala2833Thr) rs200813210 0.00003
NM_000081.4(LYST):c.8535+9A>G rs781747413 0.00001
NM_000081.4(LYST):c.*5G>A
NM_000081.4(LYST):c.10170A>G (p.Ala3390=)
NM_000081.4(LYST):c.10203A>G (p.Glu3401=)
NM_000081.4(LYST):c.10222G>A (p.Gly3408Arg)
NM_000081.4(LYST):c.10374+20A>G
NM_000081.4(LYST):c.10459C>T (p.Gln3487Ter)
NM_000081.4(LYST):c.10468G>A (p.Gly3490Arg)
NM_000081.4(LYST):c.10848A>G (p.Thr3616=)
NM_000081.4(LYST):c.10965G>A (p.Ala3655=) rs762254542
NM_000081.4(LYST):c.11229A>G (p.Arg3743=)
NM_000081.4(LYST):c.1481C>T (p.Ser494Leu)
NM_000081.4(LYST):c.1722A>G (p.Leu574=)
NM_000081.4(LYST):c.1758_1761dup (p.Pro588fs)
NM_000081.4(LYST):c.2058G>C (p.Leu686Phe)
NM_000081.4(LYST):c.2310T>C (p.Pro770=)
NM_000081.4(LYST):c.2319G>A (p.Val773=)
NM_000081.4(LYST):c.2455G>A (p.Ala819Thr)
NM_000081.4(LYST):c.2465C>T (p.Thr822Ile)
NM_000081.4(LYST):c.2720del (p.Leu907fs)
NM_000081.4(LYST):c.2844C>T (p.Ser948=)
NM_000081.4(LYST):c.285T>G (p.Asp95Glu) rs747965676
NM_000081.4(LYST):c.2914A>T (p.Met972Leu)
NM_000081.4(LYST):c.297G>A (p.Pro99=)
NM_000081.4(LYST):c.3144A>G (p.Ile1048Met)
NM_000081.4(LYST):c.3223G>A (p.Val1075Met)
NM_000081.4(LYST):c.3249C>T (p.Ala1083=)
NM_000081.4(LYST):c.3644T>C (p.Leu1215Ser)
NM_000081.4(LYST):c.4053A>G (p.Ser1351=)
NM_000081.4(LYST):c.4221C>T (p.Asn1407=)
NM_000081.4(LYST):c.42C>T (p.Thr14=)
NM_000081.4(LYST):c.4433G>A (p.Trp1478Ter)
NM_000081.4(LYST):c.45T>C (p.Asp15=) rs1675833748
NM_000081.4(LYST):c.4670A>G (p.Asn1557Ser)
NM_000081.4(LYST):c.4779A>G (p.Gln1593=)
NM_000081.4(LYST):c.5229T>C (p.Val1743=)
NM_000081.4(LYST):c.5531A>G (p.Tyr1844Cys)
NM_000081.4(LYST):c.5923-4dup
NM_000081.4(LYST):c.5973A>G (p.Ser1991=)
NM_000081.4(LYST):c.6122-13del rs201404906
NM_000081.4(LYST):c.6192C>T (p.Ser2064=)
NM_000081.4(LYST):c.6454A>C (p.Ser2152Arg)
NM_000081.4(LYST):c.6570C>T (p.Val2190=) rs1572170906
NM_000081.4(LYST):c.6791G>C (p.Ser2264Thr)
NM_000081.4(LYST):c.7017C>T (p.Leu2339=)
NM_000081.4(LYST):c.7032A>G (p.Ser2344=)
NM_000081.4(LYST):c.7035A>G (p.Pro2345=)
NM_000081.4(LYST):c.7562G>C (p.Arg2521Thr)
NM_000081.4(LYST):c.7689C>T (p.Thr2563=)
NM_000081.4(LYST):c.8549A>G (p.Tyr2850Cys)
NM_000081.4(LYST):c.8623C>T (p.Arg2875Cys)
NM_000081.4(LYST):c.8624G>A (p.Arg2875His)
NM_000081.4(LYST):c.8657T>C (p.Ile2886Thr)
NM_000081.4(LYST):c.9319C>T (p.Arg3107Cys)
NM_000081.4(LYST):c.9387C>T (p.Thr3129=)
NM_000081.4(LYST):c.9541A>C (p.Asn3181His)
NM_000081.4(LYST):c.9702C>T (p.Gly3234=)
NM_000081.4(LYST):c.981C>A (p.Leu327=)
NM_000081.4(LYST):c.9825A>C (p.Thr3275=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.