ClinVar Miner

List of variants in gene LYST reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_000081.3(LYST):c.10110T>C (p.Ala3370=) rs886038227
NM_000081.3(LYST):c.10800+4G>T rs41308172
NM_000081.3(LYST):c.1686G>C (p.Gln562His) rs77091385
NM_000081.3(LYST):c.2769A>C (p.Ser923=) rs112739986
NM_000081.3(LYST):c.3394-14T>C rs372892911
NM_000081.3(LYST):c.368A>G (p.His123Arg)
NM_000081.3(LYST):c.3713-26G>A rs9803890
NM_000081.3(LYST):c.3989A>C (p.Asp1330Ala) rs74641549
NM_000081.3(LYST):c.463G>C (p.Val155Leu) rs769942827
NM_000081.3(LYST):c.4863-4G>A rs201382097
NM_000081.3(LYST):c.5024-43T>G rs7543060
NM_000081.3(LYST):c.5223T>C (p.Leu1741=) rs7530527
NM_000081.3(LYST):c.5461-13dup rs557545474
NM_000081.3(LYST):c.5945C>T (p.Thr1982Ile) rs146591126
NM_000081.3(LYST):c.6812A>G (p.Asp2271Gly) rs112601869
NM_000081.3(LYST):c.7059+7G>A rs111764031
NM_000081.3(LYST):c.7368T>C (p.Asn2456=) rs199631995
NM_000081.3(LYST):c.7506A>G (p.Gln2502=) rs140434436
NM_000081.3(LYST):c.7761A>G (p.Gln2587=) rs139917441
NM_000081.3(LYST):c.7870C>T (p.Arg2624Trp) rs150306354
NM_000081.3(LYST):c.9926-12C>T rs762744969

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