ClinVar Miner

List of variants in gene LYST reported by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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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.3354A>G (p.Arg1118=) rs777471673
NM_000081.4(LYST):c.440G>A (p.Arg147His) rs759868763
NM_000081.4(LYST):c.4479A>G (p.Lys1493=) rs1572269872
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.9468C>T (p.Ser3156=)
NM_000081.4(LYST):c.9958C>T (p.Arg3320Trp) rs761351181
NM_001301365.1(LYST):c.-5C>T rs141317482
NM_001301365.1(LYST):c.1655T>C (p.Val552Ala) rs199617821
NM_001301365.1(LYST):c.1686G>C (p.Gln562His) rs77091385
NM_001301365.1(LYST):c.5518T>G (p.Ser1840Ala) rs115330112
NM_001301365.1(LYST):c.6482A>C (p.Glu2161Ala) rs147756847
NM_001301365.1(LYST):c.7627+6A>T rs749282192
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.8913T>G (p.Asn2971Lys) rs34702903
NM_001301365.1(LYST):c.9017A>G (p.Lys3006Arg) rs140934482

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