ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 65
Download table as spreadsheet
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.7059+7G>A rs111764031 0.00582
NM_000081.4(LYST):c.6812A>G (p.Asp2271Gly) rs112601869 0.00580
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.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.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.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.8151T>C (p.Ile2717=) rs201045270 0.00012
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.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.10374+20A>G
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.1722A>G (p.Leu574=)
NM_000081.4(LYST):c.2310T>C (p.Pro770=)
NM_000081.4(LYST):c.2319G>A (p.Val773=)
NM_000081.4(LYST):c.2844C>T (p.Ser948=)
NM_000081.4(LYST):c.297G>A (p.Pro99=)
NM_000081.4(LYST):c.3249C>T (p.Ala1083=)
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.45T>C (p.Asp15=) rs1675833748
NM_000081.4(LYST):c.4779A>G (p.Gln1593=)
NM_000081.4(LYST):c.5229T>C (p.Val1743=)
NM_000081.4(LYST):c.5923-4dup
NM_000081.4(LYST):c.5973A>G (p.Ser1991=)
NM_000081.4(LYST):c.6192C>T (p.Ser2064=)
NM_000081.4(LYST):c.6570C>T (p.Val2190=) rs1572170906
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.8624G>A (p.Arg2875His)
NM_000081.4(LYST):c.8657T>C (p.Ile2886Thr)
NM_000081.4(LYST):c.9387C>T (p.Thr3129=)
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.