ClinVar Miner

Variants in gene ATP1A3 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 14
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HGVS dbSNP
NM_152296.5(ATP1A3):c.1080G>A (p.Thr360=) rs370511776
NM_152296.5(ATP1A3):c.1387C>T (p.Arg463Cys) rs150785666
NM_152296.5(ATP1A3):c.1500C>T (p.Ala500=) rs146606627
NM_152296.5(ATP1A3):c.153+7C>T rs782082118
NM_152296.5(ATP1A3):c.1695C>T (p.Asp565=) rs375255226
NM_152296.5(ATP1A3):c.1905C>T (p.Ala635=) rs781822752
NM_152296.5(ATP1A3):c.2319T>C (p.Asn773=) rs61733017
NM_152296.5(ATP1A3):c.2367G>A (p.Pro789=) rs372737275
NM_152296.5(ATP1A3):c.2439G>A (p.Ala813=) rs189555627
NM_152296.5(ATP1A3):c.357C>T (p.Asn119=) rs143547136
NM_152296.5(ATP1A3):c.6+3A>G rs369853936
NM_152296.5(ATP1A3):c.666T>G (p.Thr222=) rs2217342
NM_152296.5(ATP1A3):c.909C>T (p.Leu303=) rs782266448
NM_152296.5(ATP1A3):c.994-3C>G rs377256877

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