List of variants in gene NLRP12 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_144687.4(NLRP12):c.1437G>A (p.Gln479=)	rs77667763	0.00294
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.1953G>A (p.Ser651=)	rs771048449
NM_144687.4(NLRP12):c.1998T>C (p.Tyr666=)	rs1297936600
NM_144687.4(NLRP12):c.2072+2dup	rs104895565
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.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

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