ClinVar Miner

List of variants in gene LRPPRC reported as likely benign by GeneDx

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Total variants: 68
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HGVS dbSNP
NM_133259.4(LRPPRC):c.-33G>A rs1162042995
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.1184A>G (p.Lys395Arg) rs781185542
NM_133259.4(LRPPRC):c.1209C>T (p.His403=) rs375528620
NM_133259.4(LRPPRC):c.1236T>C (p.His412=) rs764634151
NM_133259.4(LRPPRC):c.1253A>G (p.Asn418Ser) rs373908553
NM_133259.4(LRPPRC):c.1261+8A>G rs1572565987
NM_133259.4(LRPPRC):c.1262-12T>C rs149449510
NM_133259.4(LRPPRC):c.1369+20C>T rs371260395
NM_133259.4(LRPPRC):c.1421A>G (p.Gln474Arg) rs201339004
NM_133259.4(LRPPRC):c.1488+40A>T rs201360053
NM_133259.4(LRPPRC):c.149+8C>T rs548205703
NM_133259.4(LRPPRC):c.150-19del rs777754167
NM_133259.4(LRPPRC):c.151G>C (p.Gly51Arg) rs199606252
NM_133259.4(LRPPRC):c.1582+20G>A rs373269119
NM_133259.4(LRPPRC):c.1583-14A>G rs372371276
NM_133259.4(LRPPRC):c.1583-17G>A rs1410002648
NM_133259.4(LRPPRC):c.1649+11C>T rs200115839
NM_133259.4(LRPPRC):c.1650-18C>A rs1553404839
NM_133259.4(LRPPRC):c.1677+11C>T rs58811869
NM_133259.4(LRPPRC):c.1677+18T>A rs779816604
NM_133259.4(LRPPRC):c.1677+294C>A rs144340094
NM_133259.4(LRPPRC):c.1842+10C>T rs373649496
NM_133259.4(LRPPRC):c.1915A>G (p.Ile639Val) rs863224050
NM_133259.4(LRPPRC):c.1966-12del rs763457460
NM_133259.4(LRPPRC):c.2079+10G>A rs545497810
NM_133259.4(LRPPRC):c.2210+10C>T rs200747013
NM_133259.4(LRPPRC):c.2271A>G (p.Val757=) rs145963884
NM_133259.4(LRPPRC):c.2364C>T (p.Ser788=) rs143672315
NM_133259.4(LRPPRC):c.2373C>T (p.His791=) rs1572950032
NM_133259.4(LRPPRC):c.2388A>G (p.Ala796=) rs781484771
NM_133259.4(LRPPRC):c.242A>G (p.Asn81Ser) rs748138102
NM_133259.4(LRPPRC):c.2487C>T (p.Val829=) rs527287371
NM_133259.4(LRPPRC):c.2504+128G>C rs75856196
NM_133259.4(LRPPRC):c.2504+17T>C rs1057523262
NM_133259.4(LRPPRC):c.2563T>C (p.Leu855=) rs749500498
NM_133259.4(LRPPRC):c.2629+12T>G rs367880065
NM_133259.4(LRPPRC):c.2629+18A>G rs572783698
NM_133259.4(LRPPRC):c.262A>C (p.Met88Leu) rs863224049
NM_133259.4(LRPPRC):c.3030C>T (p.Asp1010=) rs147000685
NM_133259.4(LRPPRC):c.3078G>A (p.Ser1026=) rs760063530
NM_133259.4(LRPPRC):c.3148+14G>A rs555356354
NM_133259.4(LRPPRC):c.3275+7G>A rs111392631
NM_133259.4(LRPPRC):c.3365-16T>C rs377145600
NM_133259.4(LRPPRC):c.3570-188A>T rs114392725
NM_133259.4(LRPPRC):c.3585C>T (p.Ala1195=) rs139109482
NM_133259.4(LRPPRC):c.365A>G (p.His122Arg) rs767831585
NM_133259.4(LRPPRC):c.3825+299A>G rs115280310
NM_133259.4(LRPPRC):c.3826-16_3826-14dup rs1553390388
NM_133259.4(LRPPRC):c.3837A>G (p.Ala1279=) rs1000290192
NM_133259.4(LRPPRC):c.3900+193G>T rs116104003
NM_133259.4(LRPPRC):c.3901-14A>G rs764713386
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.4077C>T (p.Tyr1359=) rs148828179
NM_133259.4(LRPPRC):c.408A>G (p.Glu136=) rs769912947
NM_133259.4(LRPPRC):c.4129-8C>T rs1553387459
NM_133259.4(LRPPRC):c.470-13A>G rs201627660
NM_133259.4(LRPPRC):c.470-20A>G rs201123932
NM_133259.4(LRPPRC):c.525T>C (p.Asn175=) rs570349090
NM_133259.4(LRPPRC):c.651-15G>A rs375831894
NM_133259.4(LRPPRC):c.66C>T (p.Leu22=) rs769158010
NM_133259.4(LRPPRC):c.723G>A (p.Gly241=) rs371182328
NM_133259.4(LRPPRC):c.814G>A (p.Ala272Thr) rs200061143
NM_133259.4(LRPPRC):c.864+11T>G rs193090896
NM_133259.4(LRPPRC):c.94G>C (p.Gly32Arg) rs863224051

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