ClinVar Miner

List of variants in gene NLRP12 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_144687.4(NLRP12):c.-12C>T rs4539722 0.44990
NM_144687.4(NLRP12):c.116G>T (p.Gly39Val) rs34436714 0.22387
NM_144687.4(NLRP12):c.1206C>G (p.Phe402Leu) rs34971363 0.05162
NM_144687.4(NLRP12):c.289+18C>T rs116129563 0.03610
NM_144687.4(NLRP12):c.969T>G (p.Leu323=) rs142063194 0.00814
NM_144687.4(NLRP12):c.2754G>C (p.Leu918=) rs61741347 0.00692
NM_144687.4(NLRP12):c.3046C>T (p.Arg1016Ter) rs35064500 0.00470
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.1063G>A (p.Glu355Lys) rs143855597 0.00161
NM_144687.4(NLRP12):c.3004G>A (p.Asp1002Asn) rs144746100 0.00131
NM_144687.4(NLRP12):c.2579C>G (p.Thr860Ser) rs150671525 0.00069
NM_144687.4(NLRP12):c.2309A>C (p.Lys770Thr) rs138493915 0.00056
NM_144687.4(NLRP12):c.298C>T (p.Pro100Ser) rs200813801 0.00041
NM_144687.4(NLRP12):c.2384G>A (p.Arg795Gln) rs373954247 0.00040
NM_144687.4(NLRP12):c.2442G>A (p.Gly814=) rs140247843 0.00036
NM_144687.4(NLRP12):c.412C>T (p.Arg138Trp) rs142971951 0.00032
NM_144687.4(NLRP12):c.779C>T (p.Thr260Met) rs150280940 0.00027
NM_144687.4(NLRP12):c.629C>T (p.Pro210Leu) rs377594629 0.00021
NM_144687.4(NLRP12):c.1854C>G (p.Tyr618Ter) rs142487599 0.00013
NM_144687.4(NLRP12):c.2748G>A (p.Gln916=) rs368633277 0.00013
NM_144687.4(NLRP12):c.2340C>T (p.Asn780=) rs371264069 0.00011
NM_144687.4(NLRP12):c.3000G>C (p.Leu1000Phe) rs201437704 0.00011
NM_144687.4(NLRP12):c.3128C>T (p.Thr1043Ile) rs143874173 0.00011
NM_144687.4(NLRP12):c.1820A>C (p.Gln607Pro) rs370229918 0.00010
NM_144687.4(NLRP12):c.2073-3C>A rs756794505 0.00005
NM_144687.4(NLRP12):c.14C>A (p.Ala5Glu) rs761545315 0.00004
NM_144687.4(NLRP12):c.622G>A (p.Glu208Lys) rs751219722 0.00003
NM_144687.4(NLRP12):c.550G>A (p.Ala184Thr) rs766308091 0.00002
NM_144687.4(NLRP12):c.632G>A (p.Arg211His) rs374108426 0.00002
NM_144687.4(NLRP12):c.1425A>G (p.Leu475=) rs199475865 0.00001
NM_144687.4(NLRP12):c.1204T>C (p.Phe402Leu)
NM_144687.4(NLRP12):c.1538T>A (p.Ile513Asn)
NM_144687.4(NLRP12):c.1834G>A (p.Glu612Lys) rs2122658928
NM_144687.4(NLRP12):c.2185G>A (p.Gly729Arg) rs139938997
NM_144687.4(NLRP12):c.2228A>G (p.Lys743Arg)
NM_144687.4(NLRP12):c.2469C>A (p.Leu823=) rs12460528
NM_144687.4(NLRP12):c.2469C>T (p.Leu823=) rs12460528
NM_144687.4(NLRP12):c.2532G>A (p.Leu844=)
NM_144687.4(NLRP12):c.2825A>G (p.Asn942Ser) rs1220727074
NM_144687.4(NLRP12):c.2828_2829dup (p.Arg944fs) rs533054990
NM_144687.4(NLRP12):c.2830C>A (p.Arg944=) rs104895570
NM_144687.4(NLRP12):c.2927+4_2927+5dup rs763190690
NM_144687.4(NLRP12):c.3088C>G (p.Arg1030Gly) rs201619538
NM_144687.4(NLRP12):c.3176T>C (p.Ile1059Thr)
NM_144687.4(NLRP12):c.46dup (p.Tyr16fs) rs1599879570
NM_144687.4(NLRP12):c.709G>C (p.Gly237Arg)
NM_144687.4(NLRP12):c.912C>A (p.His304Gln)

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