ClinVar Miner

List of variants in gene PDYN reported as uncertain significance by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_024411.5(PDYN):c.59C>T (p.Ala20Val) rs146598522 0.00013
NM_024411.5(PDYN):c.476G>A (p.Gly159Asp) rs144748816 0.00009
NM_024411.5(PDYN):c.71C>T (p.Ser24Leu) rs201321347 0.00008
NM_024411.5(PDYN):c.520C>T (p.Arg174Cys) rs567558964 0.00007
NM_024411.5(PDYN):c.616C>T (p.Arg206Cys) rs575606358 0.00006
NM_024411.5(PDYN):c.74G>A (p.Arg25Gln) rs369559888 0.00005
NM_024411.5(PDYN):c.490G>A (p.Ala164Thr) rs376124198 0.00004
NM_024411.5(PDYN):c.365T>C (p.Leu122Pro) rs140611042 0.00003
NM_024411.5(PDYN):c.65G>A (p.Cys22Tyr) rs773876922 0.00003
NM_024411.5(PDYN):c.724G>A (p.Glu242Lys) rs1181111571 0.00002
NM_024411.5(PDYN):c.137C>T (p.Ser46Phe) rs770746350 0.00001
NM_024411.5(PDYN):c.154G>A (p.Ala52Thr) rs781650898 0.00001
NM_024411.5(PDYN):c.257C>T (p.Ser86Leu) rs781363760 0.00001
NM_024411.5(PDYN):c.2T>C (p.Met1Thr) rs1222261993 0.00001
NM_024411.5(PDYN):c.321G>T (p.Glu107Asp) rs761883755 0.00001
NM_024411.5(PDYN):c.385A>C (p.Lys129Gln) rs1987706502 0.00001
NM_024411.5(PDYN):c.437T>A (p.Met146Lys) rs751547542 0.00001
NM_024411.5(PDYN):c.457G>A (p.Asp153Asn) rs1171241754 0.00001
NM_024411.5(PDYN):c.530G>A (p.Gly177Asp) rs781094877 0.00001
NM_024411.5(PDYN):c.637C>T (p.Arg213Cys) rs150455107 0.00001
NM_024411.5(PDYN):c.650A>G (p.Lys217Arg) rs1214670418 0.00001
NM_024411.5(PDYN):c.660G>A (p.Trp220Ter) rs774412599 0.00001
NM_024411.5(PDYN):c.695G>A (p.Arg232His) rs774175877 0.00001
NM_024411.5(PDYN):c.727G>A (p.Asp243Asn) rs2122303556 0.00001
NM_024411.5(PDYN):c.731C>T (p.Pro244Leu) rs765854641 0.00001
NM_024411.5(PDYN):c.73C>T (p.Arg25Trp) rs1028619685 0.00001
NM_024411.5(PDYN):c.746G>A (p.Gly249Glu) rs772841725 0.00001
NM_024411.5(PDYN):c.88G>A (p.Ala30Thr) rs779267247 0.00001
NC_000020.10:g.(?_1959939)_(1963730_?)dup
NC_000020.10:g.(?_1960969)_(1963730_?)del
NM_024411.5(PDYN):c.104A>G (p.Asp35Gly) rs2514350514
NM_024411.5(PDYN):c.129+3A>G rs2514350236
NM_024411.5(PDYN):c.17T>C (p.Leu6Pro)
NM_024411.5(PDYN):c.209C>A (p.Thr70Asn)
NM_024411.5(PDYN):c.209C>T (p.Thr70Ile) rs759270820
NM_024411.5(PDYN):c.220C>G (p.Leu74Val)
NM_024411.5(PDYN):c.338C>G (p.Pro113Arg) rs2514337531
NM_024411.5(PDYN):c.347C>G (p.Ser116Ter) rs1987710238
NM_024411.5(PDYN):c.34del (p.Leu12fs) rs761385412
NM_024411.5(PDYN):c.41T>A (p.Met14Lys) rs1600515313
NM_024411.5(PDYN):c.422C>T (p.Ala141Val) rs2514336805
NM_024411.5(PDYN):c.538C>A (p.Arg180Ser) rs370283678
NM_024411.5(PDYN):c.539G>A (p.Arg180His) rs377075531
NM_024411.5(PDYN):c.547C>A (p.Pro183Thr) rs1987686544
NM_024411.5(PDYN):c.566T>G (p.Val189Gly) rs773424079
NM_024411.5(PDYN):c.568G>T (p.Ala190Ser) rs2122307518
NM_024411.5(PDYN):c.584G>A (p.Gly195Glu) rs2122307068
NM_024411.5(PDYN):c.596G>C (p.Gly199Ala) rs949868832
NM_024411.5(PDYN):c.623G>A (p.Gly208Glu) rs2514334574
NM_024411.5(PDYN):c.80C>T (p.Ser27Phe) rs536626217

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