ClinVar Miner

Variants in gene ANO10 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 11
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HGVS dbSNP gnomAD frequency
NM_018075.5(ANO10):c.1385G>A (p.Arg462Gln) rs3772165 0.58882
NM_018075.5(ANO10):c.1066A>G (p.Ser356Gly) rs56389778 0.05750
NM_018075.5(ANO10):c.1682C>T (p.Thr561Met) rs17409162 0.04859
NM_018075.5(ANO10):c.788G>A (p.Arg263His) rs41289586 0.01896
NM_018075.5(ANO10):c.74A>C (p.Gln25Pro) rs112040665 0.01413
NM_018075.5(ANO10):c.1915-5816C>A rs146629436 0.00245
NM_018075.5(ANO10):c.963C>T (p.Phe321=) rs149196477 0.00097
NM_018075.5(ANO10):c.1914+3G>A rs113187031 0.00068
NM_018075.5(ANO10):c.1219-23dup rs367784953
NM_018075.5(ANO10):c.159A>G (p.Arg53=) rs533186096
NM_018075.5(ANO10):c.1683G>C (p.Thr561=) rs141040660

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