ClinVar Miner

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

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Total variants: 20
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HGVS dbSNP
NM_133259.3(LRPPRC):c.592_603delGTGACATACCAG (p.Val198_Gln201del)
NM_133259.4(LRPPRC):c.109G>T (p.Ala37Ser) rs763948159
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.1211C>A (p.Ser404Tyr) rs148016991
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.1426A>G (p.Thr476Ala) rs115507225
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.2861G>A (p.Arg954Lys) rs863224060
NM_133259.4(LRPPRC):c.2965C>T (p.Arg989Cys) rs199706677
NM_133259.4(LRPPRC):c.2981G>C (p.Arg994Thr) rs912716897
NM_133259.4(LRPPRC):c.3034C>T (p.Pro1012Ser) rs113374262
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.7G>A (p.Ala3Thr) rs200686732
NM_133259.4(LRPPRC):c.908G>A (p.Arg303His) rs745653250

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