ClinVar Miner

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

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Total variants: 22
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HGVS dbSNP
NM_133259.4(LRPPRC):c.-11A>G rs188424940
NM_133259.4(LRPPRC):c.1432A>G (p.Thr478Ala) rs35035668
NM_133259.4(LRPPRC):c.1488+16G>A rs200299073
NM_133259.4(LRPPRC):c.149+19T>C rs531535255
NM_133259.4(LRPPRC):c.149+20C>G rs540850536
NM_133259.4(LRPPRC):c.1491A>T (p.Glu497Asp) rs571886021
NM_133259.4(LRPPRC):c.1529C>G (p.Ala510Gly) rs115693730
NM_133259.4(LRPPRC):c.1736-14G>A rs116117684
NM_133259.4(LRPPRC):c.1888C>T (p.Leu630=) rs35881858
NM_133259.4(LRPPRC):c.2118A>G (p.Glu706=) rs118188415
NM_133259.4(LRPPRC):c.2325A>G (p.Lys775=) rs139634347
NM_133259.4(LRPPRC):c.2481A>G (p.Pro827=) rs115993634
NM_133259.4(LRPPRC):c.2562A>G (p.Val854=) rs4494798
NM_133259.4(LRPPRC):c.2896+16A>G rs117077213
NM_133259.4(LRPPRC):c.347-19A>G rs78083883
NM_133259.4(LRPPRC):c.3570-3C>T rs35113761
NM_133259.4(LRPPRC):c.3595A>G (p.Asn1199Asp) rs113974315
NM_133259.4(LRPPRC):c.3825+15C>T rs374967275
NM_133259.4(LRPPRC):c.41C>G (p.Ala14Gly) rs114205971
NM_133259.4(LRPPRC):c.58C>T (p.Leu20Phe) rs184339274
NM_133259.4(LRPPRC):c.64C>G (p.Leu22Val) rs181626399
NM_133259.4(LRPPRC):c.79C>T (p.Leu27Phe) rs116727742

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