ClinVar Miner

List of variants in gene CCNO reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_021147.5(CCNO):c.187T>C (p.Ser63Pro) rs377241996 0.00046
NM_021147.5(CCNO):c.62A>G (p.Asn21Ser) rs748757403 0.00015
NM_021147.5(CCNO):c.950T>C (p.Met317Thr) rs145783643 0.00011
NM_021147.5(CCNO):c.206A>G (p.Asp69Gly) rs372247606 0.00008
NM_021147.5(CCNO):c.688G>A (p.Ala230Thr) rs553351741 0.00005
NM_021147.5(CCNO):c.607C>G (p.Leu203Val) rs764800405 0.00004
NM_021147.5(CCNO):c.188C>A (p.Ser63Tyr) rs774547104 0.00003
NM_021147.5(CCNO):c.787C>T (p.Arg263Trp) rs771099683 0.00003
NM_021147.5(CCNO):c.131A>G (p.His44Arg) rs369888352 0.00002
NM_021147.5(CCNO):c.26C>T (p.Pro9Leu) rs776702978 0.00001
NM_021147.5(CCNO):c.317A>C (p.Tyr106Ser) rs1375638595 0.00001
NM_021147.5(CCNO):c.587G>T (p.Arg196Leu) rs756994700 0.00001
NM_021147.5(CCNO):c.724C>T (p.His242Tyr) rs1745584991 0.00001
NM_021147.5(CCNO):c.1040C>G (p.Pro347Arg) rs547968661
NM_021147.5(CCNO):c.118A>C (p.Lys40Gln)
NM_021147.5(CCNO):c.118A>G (p.Lys40Glu)
NM_021147.5(CCNO):c.133C>G (p.Pro45Ala)
NM_021147.5(CCNO):c.19A>C (p.Thr7Pro) rs2478557102
NM_021147.5(CCNO):c.224C>T (p.Ser75Phe) rs1240616819
NM_021147.5(CCNO):c.226G>A (p.Ala76Thr)
NM_021147.5(CCNO):c.40G>T (p.Ala14Ser) rs1745666050
NM_021147.5(CCNO):c.412A>G (p.Ser138Gly)
NM_021147.5(CCNO):c.54G>C (p.Arg18Ser)
NM_021147.5(CCNO):c.581C>T (p.Pro194Leu)
NM_021147.5(CCNO):c.607C>A (p.Leu203Ile)
NM_021147.5(CCNO):c.776A>C (p.Gln259Pro) rs1745581917
NM_021147.5(CCNO):c.778G>T (p.Ala260Ser) rs2478543493
NM_021147.5(CCNO):c.793G>A (p.Val265Met)
NM_021147.5(CCNO):c.869T>A (p.Leu290Gln)
NM_021147.5(CCNO):c.986C>T (p.Thr329Ile)

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