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: 16
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HGVS dbSNP
NM_152296.4(ATP1A3):c.1131A>G (p.Thr377=) rs143242360
NM_152296.4(ATP1A3):c.1281G>A (p.Gln427=) rs116979196
NM_152296.4(ATP1A3):c.1323G>A (p.Ala441=) rs34578730
NM_152296.4(ATP1A3):c.147T>C (p.Cys49=) rs376960579
NM_152296.4(ATP1A3):c.1527C>T (p.Ser509=) rs199625170
NM_152296.4(ATP1A3):c.207A>T (p.Ala69=) rs200616931
NM_152296.4(ATP1A3):c.2319T>C (p.Asn773=) rs61733017
NM_152296.4(ATP1A3):c.2334G>A (p.Thr778=) rs145374789
NM_152296.4(ATP1A3):c.2419-7C>T rs187436315
NM_152296.4(ATP1A3):c.2487G>A (p.Pro829=) rs45606534
NM_152296.4(ATP1A3):c.2610C>T (p.Pro870=) rs35272495
NM_152296.4(ATP1A3):c.357C>T (p.Asn119=) rs143547136
NM_152296.4(ATP1A3):c.363C>T (p.Tyr121=) rs373180830
NM_152296.4(ATP1A3):c.6+3A>G rs369853936
NM_152296.4(ATP1A3):c.666T>G (p.Thr222=) rs2217342
NM_152296.5(ATP1A3):c.154-5C>G rs191645384

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