ClinVar Miner

List of variants in gene ATP1A2 reported as benign for Familial hemiplegic migraine

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Total variants: 21
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HGVS dbSNP
NM_000702.3(ATP1A2):c.*1496delA rs138196662
NM_000702.3(ATP1A2):c.1119G>A (p.Ser373=) rs1063125
NM_000702.3(ATP1A2):c.1125G>A (p.Lys375=) rs61734526
NM_000702.3(ATP1A2):c.1203C>T (p.Thr401=) rs547954866
NM_000702.3(ATP1A2):c.129G>A (p.Lys43=) rs61734527
NM_000702.3(ATP1A2):c.13-11_13-8delTCCT rs373796693
NM_000702.3(ATP1A2):c.1470C>T (p.Ile490=) rs111405592
NM_000702.3(ATP1A2):c.1652-7C>G rs200102433
NM_000702.3(ATP1A2):c.1704C>T (p.Phe568=) rs17846714
NM_000702.3(ATP1A2):c.1761T>C (p.Ser587=) rs199621678
NM_000702.3(ATP1A2):c.194G>T (p.Arg65Leu) rs187733403
NM_000702.3(ATP1A2):c.1980C>T (p.Cys660=) rs61734529
NM_000702.3(ATP1A2):c.2259C>T (p.Ala753=) rs17846715
NM_000702.3(ATP1A2):c.2563+4C>T rs3747626
NM_000702.3(ATP1A2):c.2564-8A>G rs554846350
NM_000702.3(ATP1A2):c.25T>A (p.Tyr9Asn) rs55858252
NM_000702.3(ATP1A2):c.2751G>A (p.Thr917=) rs146839867
NM_000702.3(ATP1A2):c.2961C>T (p.Cys987=) rs74123254
NM_000702.3(ATP1A2):c.2967C>T (p.Phe989=) rs138826759
NM_000702.3(ATP1A2):c.340G>A (p.Gly114Ser) rs116711766
NM_000702.3(ATP1A2):c.471T>C (p.Asp157=) rs553035942

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