ClinVar Miner

List of variants in gene NLRP12 reported as likely benign for not provided

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Gene type:
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Total variants: 40
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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.1437G>A (p.Gln479=) rs77667763 0.00294
NM_144687.4(NLRP12):c.2141A>G (p.Asn714Ser) rs150848917 0.00278
NM_144687.4(NLRP12):c.2927+14A>G rs199476247 0.00247
NM_144687.4(NLRP12):c.1299A>G (p.Ala433=) rs73608455 0.00194
NM_144687.4(NLRP12):c.819T>C (p.Pro273=) rs59749540 0.00191
NM_144687.4(NLRP12):c.1352G>A (p.Arg451His) rs76085152 0.00188
NM_144687.4(NLRP12):c.3024C>T (p.Asn1008=) rs140769141 0.00142
NM_144687.3(NLRP12):c.-143C>A rs190223587 0.00121
NM_144687.4(NLRP12):c.559G>A (p.Val187Met) rs147355465 0.00042
NM_144687.4(NLRP12):c.779C>T (p.Thr260Met) rs150280940 0.00027
NM_144687.4(NLRP12):c.2673G>A (p.Leu891=) rs201832323 0.00017
NM_144687.4(NLRP12):c.2600G>A (p.Arg867His) rs140731275 0.00013
NM_144687.4(NLRP12):c.831G>A (p.Ala277=) rs371391087 0.00013
NM_144687.4(NLRP12):c.2340C>T (p.Asn780=) rs371264069 0.00011
NM_144687.4(NLRP12):c.552G>A (p.Ala184=) rs367744369 0.00011
NM_144687.4(NLRP12):c.236G>A (p.Arg79Gln) rs144936138 0.00010
NM_144687.4(NLRP12):c.752A>G (p.Asn251Ser) rs200679354 0.00005
NM_144687.4(NLRP12):c.2052G>A (p.Ala684=) rs755768331 0.00003
NM_144687.4(NLRP12):c.308C>T (p.Pro103Leu) rs141436635 0.00003
NM_144687.4(NLRP12):c.1824G>A (p.Gln608=) rs1308512408 0.00002
NM_144687.4(NLRP12):c.1035G>A (p.Thr345=) rs770310990 0.00001
NM_144687.4(NLRP12):c.1341G>A (p.Pro447=) rs577056280 0.00001
NM_144687.4(NLRP12):c.2927+10G>A rs759672572 0.00001
NM_144687.4(NLRP12):c.66T>C (p.Ala22=) rs376521503 0.00001
NM_144687.4(NLRP12):c.1197C>T (p.Thr399=)
NM_144687.4(NLRP12):c.1395G>C (p.Ala465=) rs1448398172
NM_144687.4(NLRP12):c.1953G>A (p.Ser651=) rs771048449
NM_144687.4(NLRP12):c.1956C>T (p.Phe652=) rs1359119829
NM_144687.4(NLRP12):c.1998T>C (p.Tyr666=) rs1297936600
NM_144687.4(NLRP12):c.2072+2dup rs104895565
NM_144687.4(NLRP12):c.2511T>C (p.Asn837=) rs1250922737
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.2830C>T (p.Arg944Trp) rs104895570
NM_144687.4(NLRP12):c.2927+4_2927+5dup rs763190690
NM_144687.4(NLRP12):c.2991C>T (p.Asn997=) rs1334288624
NM_144687.4(NLRP12):c.306C>T (p.Gly102=) rs745452377
NM_144687.4(NLRP12):c.627A>G (p.Pro209=) rs2122680445
NM_144687.4(NLRP12):c.975C>T (p.Asn325=) rs1599843036

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