ClinVar Miner

List of variants in gene LYST reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_000081.4(LYST):c.5945C>T (p.Thr1982Ile) rs146591126 0.00669
NM_000081.4(LYST):c.10941-7C>A rs72761794 0.00614
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.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.8913T>G (p.Asn2971Lys) rs34702903 0.00276
NM_000081.4(LYST):c.2363+4T>C rs201398337 0.00252
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.8487C>T (p.Ile2829=) rs144597913 0.00126
NM_000081.4(LYST):c.7506A>G (p.Gln2502=) rs140434436 0.00106
NM_000081.4(LYST):c.6588A>G (p.Gly2196=) rs34423788 0.00093
NM_000081.4(LYST):c.3507C>T (p.Leu1169=) rs74861744 0.00083
NM_000081.4(LYST):c.11086G>A (p.Val3696Ile) rs147221131 0.00052
NM_000081.4(LYST):c.8806G>A (p.Val2936Ile) rs2753327 0.00052
NM_000081.4(LYST):c.9017A>G (p.Lys3006Arg) rs140934482 0.00047
NM_000081.4(LYST):c.143A>G (p.His48Arg) rs200132460 0.00046
NM_000081.4(LYST):c.1655T>C (p.Val552Ala) rs199617821 0.00038
NM_000081.4(LYST):c.8960C>G (p.Pro2987Arg) rs147899661 0.00032
NM_000081.4(LYST):c.6782G>A (p.Arg2261His) rs147791378 0.00031
NM_000081.4(LYST):c.8268C>T (p.His2756=) rs141534829 0.00029
NM_000081.4(LYST):c.6487G>A (p.Ala2163Thr) rs201513511 0.00026
NM_000081.4(LYST):c.4578T>A (p.Asn1526Lys) rs117609949 0.00025
NM_000081.4(LYST):c.2754G>A (p.Glu918=) rs373577384 0.00022
NM_000081.4(LYST):c.6291C>T (p.Ala2097=) rs199857997 0.00016
NM_000081.4(LYST):c.7806A>G (p.Gln2602=) rs372754364 0.00014
NM_000081.4(LYST):c.4513A>G (p.Ile1505Val) rs756527927 0.00011
NM_000081.4(LYST):c.7627+6A>T rs749282192 0.00008
NM_000081.4(LYST):c.7862T>C (p.Met2621Thr) rs368500877 0.00006
NM_000081.4(LYST):c.1541G>A (p.Arg514Gln) rs564745712 0.00004
NM_000081.4(LYST):c.3876A>G (p.Val1292=) rs144664809 0.00004
NM_000081.4(LYST):c.5061T>C (p.Tyr1687=) rs80338658 0.00004
NM_000081.4(LYST):c.8607A>G (p.Gln2869=) rs369484787 0.00004
NM_000081.4(LYST):c.10870G>A (p.Val3624Ile) rs776033238 0.00003
NM_000081.4(LYST):c.3354A>G (p.Arg1118=) rs777471673 0.00002
NM_000081.4(LYST):c.7631T>C (p.Met2544Thr) rs1371610729 0.00002
NM_000081.4(LYST):c.9834T>C (p.Thr3278=) rs901343967 0.00002
NM_000081.4(LYST):c.440G>A (p.Arg147His) rs759868763 0.00001
NM_000081.4(LYST):c.463G>C (p.Val155Leu) rs769942827 0.00001
NM_000081.4(LYST):c.*1295T>C
NM_000081.4(LYST):c.*1831A>C
NM_000081.4(LYST):c.*891G>C
NM_000081.4(LYST):c.10669G>T (p.Val3557Leu)
NM_000081.4(LYST):c.11355C>G (p.Arg3785=)
NM_000081.4(LYST):c.1836G>A (p.Leu612=)
NM_000081.4(LYST):c.1995A>G (p.Ser665=)
NM_000081.4(LYST):c.244C>T (p.Leu82=)
NM_000081.4(LYST):c.42C>T (p.Thr14=)
NM_000081.4(LYST):c.4479A>G (p.Lys1493=) rs1572269872
NM_000081.4(LYST):c.4893T>C (p.Leu1631=)
NM_000081.4(LYST):c.6898T>C (p.Leu2300=)
NM_000081.4(LYST):c.7677del (p.Phe2559fs) rs2103306487
NM_000081.4(LYST):c.8033C>G (p.Thr2678Ser)
NM_000081.4(LYST):c.9468C>T (p.Ser3156=) rs1663290633
NM_000081.4(LYST):c.9699T>C (p.Tyr3233=)

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