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

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: 51

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HGVS	dbSNP	gnomAD frequency
NM_133259.4(LRPPRC):c.246G>A (p.Gln82=)	rs6741066	0.69341
NM_133259.4(LRPPRC):c.1068A>G (p.Gln356=)	rs4953042	0.14931
NM_133259.4(LRPPRC):c.2562A>G (p.Val854=)	rs4494798	0.01150
NM_133259.4(LRPPRC):c.470-20A>G	rs201123932	0.00208
NM_133259.4(LRPPRC):c.3275+7G>A	rs111392631	0.00152
NM_133259.4(LRPPRC):c.149+8C>T	rs548205703	0.00098
NM_133259.4(LRPPRC):c.2211-14G>A	rs375399789	0.00046
NM_133259.4(LRPPRC):c.1842+10C>T	rs373649496	0.00040
NM_133259.4(LRPPRC):c.3585C>T (p.Ala1195=)	rs139109482	0.00035
NM_133259.4(LRPPRC):c.651-15G>A	rs375831894	0.00032
NM_133259.4(LRPPRC):c.66C>T (p.Leu22=)	rs769158010	0.00026
NM_133259.4(LRPPRC):c.3365-16T>C	rs377145600	0.00019
NM_133259.4(LRPPRC):c.1583-14A>G	rs372371276	0.00016
NM_133259.4(LRPPRC):c.242A>G (p.Asn81Ser)	rs748138102	0.00011
NM_133259.4(LRPPRC):c.1253A>G (p.Asn418Ser)	rs373908553	0.00010
NM_133259.4(LRPPRC):c.723G>A (p.Gly241=)	rs371182328	0.00007
NM_133259.4(LRPPRC):c.3078G>A (p.Ser1026=)	rs760063530	0.00006
NM_133259.4(LRPPRC):c.1369+20C>T	rs371260395	0.00004
NM_133259.4(LRPPRC):c.262A>C (p.Met88Leu)	rs863224049	0.00004
NM_133259.4(LRPPRC):c.1209C>T (p.His403=)	rs375528620	0.00003
NM_133259.4(LRPPRC):c.2079+10G>A	rs545497810	0.00002
NM_133259.4(LRPPRC):c.2629+12T>G	rs367880065	0.00002
NM_133259.4(LRPPRC):c.1184A>G (p.Lys395Arg)	rs781185542	0.00001
NM_133259.4(LRPPRC):c.1421A>G (p.Gln474Arg)	rs201339004	0.00001
NM_133259.4(LRPPRC):c.1582+20G>A	rs373269119	0.00001
NM_133259.4(LRPPRC):c.1677+18T>A	rs779816604	0.00001
NM_133259.4(LRPPRC):c.2388A>G (p.Ala796=)	rs781484771	0.00001
NM_133259.4(LRPPRC):c.2563T>C (p.Leu855=)	rs749500498	0.00001
NM_133259.4(LRPPRC):c.365A>G (p.His122Arg)	rs767831585	0.00001
NM_133259.4(LRPPRC):c.3837A>G (p.Ala1279=)	rs1000290192	0.00001
NM_133259.4(LRPPRC):c.408A>G (p.Glu136=)	rs769912947	0.00001
NM_133259.4(LRPPRC):c.814G>A (p.Ala272Thr)	rs200061143	0.00001
NM_133259.4(LRPPRC):c.1086C>A (p.Pro362=)	rs150044060
NM_133259.4(LRPPRC):c.109G>A (p.Ala37Thr)	rs763948159
NM_133259.4(LRPPRC):c.1156-13dup	rs747766605
NM_133259.4(LRPPRC):c.150-19del	rs777754167
NM_133259.4(LRPPRC):c.1583-17G>A	rs1410002648
NM_133259.4(LRPPRC):c.1650-18C>A	rs1553404839
NM_133259.4(LRPPRC):c.1677+11C>T	rs58811869
NM_133259.4(LRPPRC):c.1915A>G (p.Ile639Val)	rs863224050
NM_133259.4(LRPPRC):c.1966-12del	rs763457460
NM_133259.4(LRPPRC):c.2504+17T>C	rs1057523262
NM_133259.4(LRPPRC):c.2629+18A>G	rs572783698
NM_133259.4(LRPPRC):c.3148+14G>A	rs555356354
NM_133259.4(LRPPRC):c.3826-16_3826-14dup	rs1553390388
NM_133259.4(LRPPRC):c.3984T>C (p.Tyr1328=)	rs1057521433
NM_133259.4(LRPPRC):c.3985+14_3985+18del	rs781110277
NM_133259.4(LRPPRC):c.4129-8C>T	rs1553387459
NM_133259.4(LRPPRC):c.7G>T (p.Ala3Ser)	rs200686732
NM_133259.4(LRPPRC):c.864+11T>G	rs193090896
NM_133259.4(LRPPRC):c.94G>C (p.Gly32Arg)	rs863224051

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