ClinVar Miner

List of variants in gene LRPPRC reported as uncertain significance for not provided

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Total variants: 39
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HGVS dbSNP
NM_133259.3(LRPPRC):c.592_603delGTGACATACCAG (p.Val198_Gln201del)
NM_133259.4(LRPPRC):c.-4A>G rs1559083136
NM_133259.4(LRPPRC):c.109G>T (p.Ala37Ser) rs763948159
NM_133259.4(LRPPRC):c.1177T>G (p.Tyr393Asp) rs863224054
NM_133259.4(LRPPRC):c.1211C>A (p.Ser404Tyr) rs148016991
NM_133259.4(LRPPRC):c.1219C>G (p.Leu407Val) rs368164663
NM_133259.4(LRPPRC):c.1253A>C (p.Asn418Thr) rs373908553
NM_133259.4(LRPPRC):c.1295A>G (p.Glu432Gly) rs144732922
NM_133259.4(LRPPRC):c.1301G>A (p.Gly434Asp) rs146515622
NM_133259.4(LRPPRC):c.1390G>C (p.Gly464Arg) rs957783084
NM_133259.4(LRPPRC):c.1426A>G (p.Thr476Ala) rs115507225
NM_133259.4(LRPPRC):c.1678A>T (p.Ile560Leu) rs144826521
NM_133259.4(LRPPRC):c.1928A>G (p.His643Arg) rs148575027
NM_133259.4(LRPPRC):c.2020G>A (p.Glu674Lys) rs149243712
NM_133259.4(LRPPRC):c.2039A>T (p.Asp680Val) rs863224056
NM_133259.4(LRPPRC):c.2072C>T (p.Ser691Leu) rs372341254
NM_133259.4(LRPPRC):c.2120C>T (p.Ser707Phe) rs747145260
NM_133259.4(LRPPRC):c.2210+4A>C rs190007694
NM_133259.4(LRPPRC):c.254G>C (p.Trp85Ser)
NM_133259.4(LRPPRC):c.2569A>G (p.Arg857Gly) rs200138144
NM_133259.4(LRPPRC):c.2861G>A (p.Arg954Lys) rs863224060
NM_133259.4(LRPPRC):c.2965C>T (p.Arg989Cys) rs199706677
NM_133259.4(LRPPRC):c.2966G>C (p.Arg989Pro)
NM_133259.4(LRPPRC):c.2981G>C (p.Arg994Thr) rs912716897
NM_133259.4(LRPPRC):c.3040-4A>G rs746859840
NM_133259.4(LRPPRC):c.3275+7G>A rs111392631
NM_133259.4(LRPPRC):c.3277G>A (p.Ala1093Thr) rs200611889
NM_133259.4(LRPPRC):c.3323G>T (p.Ser1108Ile) rs1572900944
NM_133259.4(LRPPRC):c.3342A>G (p.Gln1114=) rs1572900912
NM_133259.4(LRPPRC):c.4056T>A (p.Asp1352Glu) rs146630100
NM_133259.4(LRPPRC):c.4132A>G (p.Ser1378Gly) rs149693840
NM_133259.4(LRPPRC):c.475G>A (p.Val159Met) rs1553411854
NM_133259.4(LRPPRC):c.587A>C (p.Asn196Thr) rs199727887
NM_133259.4(LRPPRC):c.620A>T (p.Tyr207Phe) rs146293544
NM_133259.4(LRPPRC):c.64C>G (p.Leu22Val) rs181626399
NM_133259.4(LRPPRC):c.719C>T (p.Thr240Ile) rs886043628
NM_133259.4(LRPPRC):c.74G>A (p.Arg25His) rs780400922
NM_133259.4(LRPPRC):c.802G>C (p.Asp268His)
NM_133259.4(LRPPRC):c.908G>A (p.Arg303His) rs745653250

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