ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_000108.5(DLD):c.788G>A (p.Arg263His) rs145670503 0.00080
NM_000108.5(DLD):c.55C>G (p.Arg19Gly) rs144038427 0.00039
NM_000108.5(DLD):c.763A>C (p.Met255Leu) rs533405046 0.00029
NM_000108.5(DLD):c.470C>G (p.Thr157Ser) rs142232609 0.00021
NM_000108.5(DLD):c.860G>A (p.Gly287Glu) rs202125745 0.00016
NM_000108.5(DLD):c.1492A>C (p.Asn498His) rs564889609 0.00006
NM_000108.5(DLD):c.764T>C (p.Met255Thr) rs185710460 0.00004
NM_000108.5(DLD):c.82T>C (p.Ser28Pro) rs768123909 0.00004
NM_000108.5(DLD):c.1382G>A (p.Gly461Glu) rs757275923 0.00003
NM_000108.5(DLD):c.1129A>G (p.Met377Val) rs915221367 0.00001
NM_000108.5(DLD):c.1502C>T (p.Ala501Val) rs527263746 0.00001
NM_000108.5(DLD):c.209T>C (p.Ile70Thr) rs373761188 0.00001
NM_000108.5(DLD):c.461G>A (p.Gly154Glu) rs759348050 0.00001
NM_000108.5(DLD):c.1193A>C (p.Glu398Ala) rs2535602664
NM_000108.5(DLD):c.1291A>G (p.Thr431Ala) rs796051952
NM_000108.5(DLD):c.263C>T (p.Ser88Phe) rs985832127
NM_000108.5(DLD):c.306T>A (p.His102Gln) rs796051950
NM_000108.5(DLD):c.656T>A (p.Ile219Asn) rs2032006962
NM_000108.5(DLD):c.722C>T (p.Ala241Val) rs796051951
NM_000108.5(DLD):c.983G>C (p.Gly328Ala)

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