ClinVar Miner

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

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001101426.4(CRPPA):c.1218T>G (p.Ile406Met) rs202011820 0.00068
NM_001101426.4(CRPPA):c.808C>T (p.Leu270Phe) rs200334999 0.00045
NM_001101426.4(CRPPA):c.532G>A (p.Gly178Arg) rs202108204 0.00011
NM_001101426.4(CRPPA):c.914T>G (p.Val305Gly) rs370397489 0.00008
NM_001101426.4(CRPPA):c.347G>A (p.Arg116His) rs748777770 0.00004
NM_001101426.4(CRPPA):c.978T>A (p.His326Gln) rs901037542 0.00003
NM_001101426.4(CRPPA):c.1045C>A (p.Gln349Lys) rs774852908 0.00001
NM_001101426.4(CRPPA):c.1161A>T (p.Lys387Asn) rs368477537 0.00001
NM_001101426.4(CRPPA):c.899A>G (p.His300Arg) rs1345477841 0.00001
NM_001101426.4(CRPPA):c.1026+1G>T rs1554300301
NM_001101426.4(CRPPA):c.245A>G (p.Gln82Arg) rs949985964
NM_001101426.4(CRPPA):c.304A>T (p.Met102Leu) rs763300192
NM_001101426.4(CRPPA):c.376C>G (p.Arg126Gly) rs1472549168
NM_001101426.4(CRPPA):c.497T>A (p.Val166Asp) rs2128318424
NM_001101426.4(CRPPA):c.536C>A (p.Ala179Glu) rs2128312092
NM_001101426.4(CRPPA):c.540A>T (p.Ala180=)
NM_001101426.4(CRPPA):c.727T>G (p.Leu243Val) rs756109539
NM_001101426.4(CRPPA):c.779A>G (p.Asp260Gly) rs1554320085
NM_001101426.4(CRPPA):c.895G>C (p.Gly299Arg) rs373890080

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