ClinVar Miner

List of variants in gene LYST reported as uncertain significance for not provided

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Gene type:
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Total variants: 33
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HGVS dbSNP
NM_000081.4(LYST):c.10870G>A (p.Val3624Ile) rs776033238
NM_000081.4(LYST):c.1541G>A (p.Arg514Gln) rs564745712
NM_000081.4(LYST):c.440G>A (p.Arg147His) rs759868763
NM_000081.4(LYST):c.4513A>G (p.Ile1505Val) rs756527927
NM_000081.4(LYST):c.4578T>A (p.Asn1526Lys) rs117609949
NM_000081.4(LYST):c.9958C>T (p.Arg3320Trp) rs761351181
NM_001301365.1(LYST):c.10235G>A (p.Arg3412His) rs148409403
NM_001301365.1(LYST):c.10286T>G (p.Ile3429Ser) rs760815034
NM_001301365.1(LYST):c.11354G>A (p.Arg3785His) rs370173269
NM_001301365.1(LYST):c.11362C>T (p.Gln3788Ter) rs1558092244
NM_001301365.1(LYST):c.1686G>C (p.Gln562His) rs77091385
NM_001301365.1(LYST):c.3083C>G (p.Ser1028Cys) rs150636017
NM_001301365.1(LYST):c.3311G>A (p.Arg1104Gln) rs148299757
NM_001301365.1(LYST):c.3461C>G (p.Thr1154Arg) rs756226516
NM_001301365.1(LYST):c.3683A>G (p.Asn1228Ser) rs145553827
NM_001301365.1(LYST):c.3710A>T (p.Asp1237Val) rs1215274878
NM_001301365.1(LYST):c.4705A>C (p.Asn1569His) rs767687843
NM_001301365.1(LYST):c.5620T>A (p.Phe1874Ile) rs757494655
NM_001301365.1(LYST):c.6388G>A (p.Asp2130Asn) rs148371004
NM_001301365.1(LYST):c.6737T>G (p.Leu2246Arg) rs200231136
NM_001301365.1(LYST):c.7070C>G (p.Ala2357Gly) rs199576020
NM_001301365.1(LYST):c.7184G>T (p.Cys2395Phe) rs760878646
NM_001301365.1(LYST):c.7627+6A>T rs749282192
NM_001301365.1(LYST):c.7780+2C>T rs760108842
NM_001301365.1(LYST):c.7862T>C (p.Met2621Thr) rs368500877
NM_001301365.1(LYST):c.7870C>T (p.Arg2624Trp) rs150306354
NM_001301365.1(LYST):c.8806G>A (p.Val2936Ile) rs2753327
NM_001301365.1(LYST):c.8913T>G (p.Asn2971Lys) rs34702903
NM_001301365.1(LYST):c.9017A>G (p.Lys3006Arg) rs140934482
NM_001301365.1(LYST):c.9045-13T>C rs181450025
NM_001301365.1(LYST):c.9520G>A (p.Val3174Ile) rs199672291
NM_001301365.1(LYST):c.9552G>T (p.Leu3184Phe) rs556200563
NM_001301365.1(LYST):c.9628-15C>T rs751859873

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