ClinVar Miner

List of variants in gene LRPPRC reported as uncertain significance by GeneDx

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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_133259.4(LRPPRC):c.1295A>G (p.Glu432Gly) rs144732922 0.00091
NM_133259.4(LRPPRC):c.1426A>G (p.Thr476Ala) rs115507225 0.00066
NM_133259.4(LRPPRC):c.151G>C (p.Gly51Arg) rs199606252 0.00029
NM_133259.4(LRPPRC):c.4132A>G (p.Ser1378Gly) rs149693840 0.00024
NM_133259.4(LRPPRC):c.620A>T (p.Tyr207Phe) rs146293544 0.00022
NM_133259.4(LRPPRC):c.908G>A (p.Arg303His) rs745653250 0.00019
NM_133259.4(LRPPRC):c.2965C>T (p.Arg989Cys) rs199706677 0.00013
NM_133259.4(LRPPRC):c.4128del (p.Glu1377fs) rs759052246 0.00010
NM_133259.4(LRPPRC):c.70C>G (p.Leu24Val) rs749629864 0.00010
NM_133259.4(LRPPRC):c.3586G>A (p.Ala1196Thr) rs142097048 0.00009
NM_133259.4(LRPPRC):c.116A>G (p.Tyr39Cys) rs1014582333 0.00007
NM_133259.4(LRPPRC):c.4056T>A (p.Asp1352Glu) rs146630100 0.00007
NM_133259.4(LRPPRC):c.802G>C (p.Asp268His) rs756849117 0.00007
NM_133259.4(LRPPRC):c.109G>T (p.Ala37Ser) rs763948159 0.00006
NM_133259.4(LRPPRC):c.1211C>A (p.Ser404Tyr) rs148016991 0.00006
NM_133259.4(LRPPRC):c.340C>G (p.Arg114Gly) rs376622590 0.00006
NM_133259.4(LRPPRC):c.2141A>G (p.Tyr714Cys) rs375559765 0.00005
NM_133259.4(LRPPRC):c.1753C>T (p.Leu585Phe) rs925345080 0.00004
NM_133259.4(LRPPRC):c.3277G>A (p.Ala1093Thr) rs200611889 0.00004
NM_133259.4(LRPPRC):c.4073G>A (p.Arg1358His) rs373807582 0.00004
NM_133259.4(LRPPRC):c.515A>G (p.Tyr172Cys) rs187584458 0.00003
NM_133259.4(LRPPRC):c.2072C>T (p.Ser691Leu) rs372341254 0.00002
NM_133259.4(LRPPRC):c.3815C>G (p.Ala1272Gly) rs370011265 0.00002
NM_133259.4(LRPPRC):c.3817C>G (p.Leu1273Val) rs200748493 0.00002
NM_133259.4(LRPPRC):c.1846G>A (p.Val616Ile) rs1229301675 0.00001
NM_133259.4(LRPPRC):c.2120C>T (p.Ser707Phe) rs747145260 0.00001
NM_133259.4(LRPPRC):c.2216G>A (p.Arg739His) rs187274438 0.00001
NM_133259.4(LRPPRC):c.110CCT[1] (p.Ser38del) rs863224061
NM_133259.4(LRPPRC):c.1177T>G (p.Tyr393Asp) rs863224054
NM_133259.4(LRPPRC):c.1253A>C (p.Asn418Thr) rs373908553
NM_133259.4(LRPPRC):c.1301G>C (p.Gly434Ala)
NM_133259.4(LRPPRC):c.140C>G (p.Pro47Arg)
NM_133259.4(LRPPRC):c.1501C>G (p.Leu501Val)
NM_133259.4(LRPPRC):c.2039A>T (p.Asp680Val) rs863224056
NM_133259.4(LRPPRC):c.205C>G (p.Gln69Glu)
NM_133259.4(LRPPRC):c.2280_2282delinsAAT (p.His761Ile)
NM_133259.4(LRPPRC):c.2297-8C>A
NM_133259.4(LRPPRC):c.2651A>T (p.Glu884Val)
NM_133259.4(LRPPRC):c.2839C>A (p.Gln947Lys)
NM_133259.4(LRPPRC):c.2861G>A (p.Arg954Lys) rs863224060
NM_133259.4(LRPPRC):c.2981G>C (p.Arg994Thr) rs912716897
NM_133259.4(LRPPRC):c.3531G>A (p.Met1177Ile) rs376046961
NM_133259.4(LRPPRC):c.3541A>G (p.Asn1181Asp)
NM_133259.4(LRPPRC):c.4022A>G (p.Tyr1341Cys)
NM_133259.4(LRPPRC):c.451G>C (p.Asp151His)
NM_133259.4(LRPPRC):c.592_603del
NM_133259.4(LRPPRC):c.613G>A (p.Ala205Thr)
NM_133259.4(LRPPRC):c.76C>T (p.Leu26Phe) rs1341115802
NM_133259.4(LRPPRC):c.79C>G (p.Leu27Val)
NM_133259.4(LRPPRC):c.7G>A (p.Ala3Thr) rs200686732
NM_133259.4(LRPPRC):c.808T>C (p.Tyr270His) rs946957597
NM_133259.4(LRPPRC):c.889G>A (p.Glu297Lys)
NM_133259.4(LRPPRC):c.956A>G (p.Gln319Arg)
NM_133259.4(LRPPRC):c.999A>G (p.Arg333=)

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