ClinVar Miner

List of variants in gene NLRP12 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_144687.4(NLRP12):c.910C>T (p.His304Tyr) rs141245482 0.00392
NM_144687.4(NLRP12):c.2701G>C (p.Val901Leu) rs104895568 0.00265
NM_144687.4(NLRP12):c.2227A>C (p.Lys743Gln) rs74373537 0.00180
NM_144687.4(NLRP12):c.1063G>A (p.Glu355Lys) rs143855597 0.00161
NM_144687.4(NLRP12):c.1731G>A (p.Lys577=) rs73608454 0.00126
NM_144687.4(NLRP12):c.2386del (p.His796fs) rs539741111 0.00102
NM_144687.4(NLRP12):c.2579C>G (p.Thr860Ser) rs150671525 0.00069
NM_144687.4(NLRP12):c.559G>A (p.Val187Met) rs147355465 0.00042
NM_144687.4(NLRP12):c.2927+11G>A rs376043494 0.00041
NM_144687.4(NLRP12):c.2384G>A (p.Arg795Gln) rs373954247 0.00040
NM_144687.4(NLRP12):c.1495A>G (p.Ile499Val) rs146903616 0.00038
NM_144687.4(NLRP12):c.629C>T (p.Pro210Leu) rs377594629 0.00021
NM_144687.4(NLRP12):c.1182C>G (p.Asn394Lys) rs201241894 0.00019
NM_144687.4(NLRP12):c.2895G>A (p.Leu965=) rs369220717 0.00013
NM_144687.4(NLRP12):c.3147G>A (p.Ala1049=) rs148506660 0.00008
NM_144687.4(NLRP12):c.78G>A (p.Lys26=) rs148263031 0.00002
NM_144687.4(NLRP12):c.1386C>T (p.Cys462=) rs1369275354 0.00001
NM_144687.4(NLRP12):c.289+14G>A rs777899039 0.00001
NM_144687.4(NLRP12):c.654G>A (p.Ala218=) rs745766441 0.00001
NM_144687.4(NLRP12):c.3015G>A (p.Leu1005=)

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