ClinVar Miner

List of variants in gene LYST reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 51
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HGVS dbSNP gnomAD frequency
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.3083C>G (p.Ser1028Cys) rs150636017 0.00049
NM_000081.4(LYST):c.10526G>A (p.Arg3509Gln) rs138936105 0.00046
NM_000081.4(LYST):c.143A>G (p.His48Arg) rs200132460 0.00046
NM_000081.4(LYST):c.3208A>G (p.Ile1070Val) rs150321124 0.00043
NM_000081.4(LYST):c.6682G>C (p.Asp2228His) rs150270086 0.00042
NM_000081.4(LYST):c.8214G>C (p.Glu2738Asp) rs140944484 0.00022
NM_000081.4(LYST):c.595G>A (p.Asp199Asn) rs552391792 0.00018
NM_000081.4(LYST):c.6388G>A (p.Asp2130Asn) rs148371004 0.00014
NM_000081.4(LYST):c.3311G>A (p.Arg1104Gln) rs148299757 0.00011
NM_000081.4(LYST):c.4513A>G (p.Ile1505Val) rs756527927 0.00011
NM_000081.4(LYST):c.9520G>A (p.Val3174Ile) rs199672291 0.00008
NM_000081.4(LYST):c.3931A>G (p.Met1311Val) rs376718077 0.00007
NM_000081.4(LYST):c.5612T>C (p.Ile1871Thr) rs559869925 0.00006
NM_000081.4(LYST):c.11354G>A (p.Arg3785His) rs370173269 0.00004
NM_000081.4(LYST):c.1290G>A (p.Met430Ile) rs779163460 0.00004
NM_000081.4(LYST):c.6737T>G (p.Leu2246Arg) rs200231136 0.00004
NM_000081.4(LYST):c.7997T>A (p.Ile2666Asn) rs369246831 0.00003
NM_000081.4(LYST):c.10286T>G (p.Ile3429Ser) rs760815034 0.00002
NM_000081.4(LYST):c.2870T>C (p.Met957Thr) rs201554916 0.00002
NM_000081.4(LYST):c.3461C>G (p.Thr1154Arg) rs756226516 0.00002
NM_000081.4(LYST):c.5833G>A (p.Ala1945Thr) rs750338502 0.00002
NM_000081.4(LYST):c.10976G>T (p.Ser3659Ile) rs1659445104 0.00001
NM_000081.4(LYST):c.11116T>A (p.Cys3706Ser) rs1481260242 0.00001
NM_000081.4(LYST):c.4288C>G (p.Arg1430Gly) rs1468055437 0.00001
NM_000081.4(LYST):c.5578A>G (p.Met1860Val) rs368738466 0.00001
NM_000081.4(LYST):c.5620T>A (p.Phe1874Ile) rs757494655 0.00001
NM_000081.4(LYST):c.7340C>T (p.Ala2447Val) rs766272501 0.00001
NM_000081.4(LYST):c.7780+2C>T rs760108842 0.00001
NM_000081.4(LYST):c.8143G>A (p.Val2715Ile) rs202010795 0.00001
NM_000081.4(LYST):c.10492G>C (p.Ala3498Pro) rs1222770569
NM_000081.4(LYST):c.10598G>C (p.Trp3533Ser)
NM_000081.4(LYST):c.11101T>G (p.Cys3701Gly) rs1658277094
NM_000081.4(LYST):c.2725G>A (p.Val909Ile)
NM_000081.4(LYST):c.285T>G (p.Asp95Glu) rs747965676
NM_000081.4(LYST):c.2909T>C (p.Ile970Thr) rs141758032
NM_000081.4(LYST):c.3137A>G (p.Asp1046Gly)
NM_000081.4(LYST):c.3650AAG[2] (p.Glu1219del) rs770679237
NM_000081.4(LYST):c.3710A>T (p.Asp1237Val) rs1215274878
NM_000081.4(LYST):c.479A>G (p.Lys160Arg) rs2102890869
NM_000081.4(LYST):c.5325C>A (p.Phe1775Leu)
NM_000081.4(LYST):c.5488A>T (p.Thr1830Ser)
NM_000081.4(LYST):c.6781C>T (p.Arg2261Cys)
NM_000081.4(LYST):c.7098A>C (p.Gln2366His) rs1013368289
NM_000081.4(LYST):c.7184G>T (p.Cys2395Phe) rs760878646
NM_000081.4(LYST):c.7485G>T (p.Leu2495Phe)
NM_000081.4(LYST):c.8161A>G (p.Lys2721Glu) rs762099794
NM_000081.4(LYST):c.8306A>G (p.His2769Arg)
NM_000081.4(LYST):c.8818C>T (p.Pro2940Ser) rs375839384
NM_000081.4(LYST):c.9233G>A (p.Arg3078His)

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