ClinVar Miner

List of variants in gene ATP1A2 studied for Familial hemiplegic migraine type 2

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Total variants: 16
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HGVS dbSNP
NM_000702.4(ATP1A2):c.1033A>G (p.Thr345Ala) rs121918613
NM_000702.4(ATP1A2):c.1127C>T (p.Thr376Met) rs121918620
NM_000702.4(ATP1A2):c.118-12T>A rs1558002572
NM_000702.4(ATP1A2):c.1244C>T (p.Thr415Met) rs121918618
NM_000702.4(ATP1A2):c.193C>T (p.Arg65Trp) rs121918619
NM_000702.4(ATP1A2):c.1980C>T (p.Cys660=) rs61734529
NM_000702.4(ATP1A2):c.2066G>A (p.Arg689Gln) rs28933401
NM_000702.4(ATP1A2):c.2152G>A (p.Asp718Asn) rs121918614
NM_000702.4(ATP1A2):c.2192T>C (p.Met731Thr) rs28933400
NM_000702.4(ATP1A2):c.2291T>C (p.Leu764Pro) rs28933398
NM_000702.4(ATP1A2):c.2438T>A (p.Met813Lys) rs796052277
NM_000702.4(ATP1A2):c.2659T>C (p.Trp887Arg) rs28933399
NM_000702.4(ATP1A2):c.2936C>T (p.Pro979Leu) rs121918615
NM_000702.4(ATP1A2):c.571G>A (p.Val191Met) rs869025341
NM_000702.4(ATP1A2):c.857T>C (p.Ile286Thr) rs121918617
NM_000702.4(ATP1A2):c.901G>A (p.Gly301Arg) rs121918612

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