ClinVar Miner

List of variants in gene DNA2 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_001080449.3(DNA2):c.507C>A (p.Ala169=) rs3758626 0.28903
NM_001080449.3(DNA2):c.357G>A (p.Leu119=) rs10998205 0.08483
NM_001080449.3(DNA2):c.1971G>A (p.Thr657=) rs61855090 0.03682
NM_001080449.3(DNA2):c.2782G>A (p.Val928Ile) rs75569266 0.03176
NM_001080449.3(DNA2):c.1899G>A (p.Ala633=) rs116704917 0.00869
NM_001080449.3(DNA2):c.1649A>G (p.Asn550Ser) rs141731085 0.00726
NM_001080449.3(DNA2):c.295T>C (p.Leu99=) rs140077857 0.00675
NM_001080449.3(DNA2):c.491A>G (p.Glu164Gly) rs114788132 0.00581
NM_001080449.3(DNA2):c.2153G>T (p.Cys718Phe) rs147096750 0.00367
NM_001080449.3(DNA2):c.720G>T (p.Leu240=) rs199878321 0.00242
NM_001080449.3(DNA2):c.2212A>G (p.Ile738Val) rs149606167 0.00177
NM_001080449.3(DNA2):c.1796G>A (p.Arg599His) rs201999986 0.00068
NM_001080449.3(DNA2):c.1476T>C (p.Cys492=) rs373089726 0.00051
NM_001080449.3(DNA2):c.2492+4T>C rs2273904 0.00014
NM_001080449.3(DNA2):c.1677G>A (p.Leu559=) rs769027938 0.00004
NM_001080449.3(DNA2):c.1503A>G (p.Gln501=) rs556056148 0.00001
NM_001080449.3(DNA2):c.1057+9G>A
NM_001080449.3(DNA2):c.1057+9G>T rs757243525
NM_001080449.3(DNA2):c.1221-9T>C
NM_001080449.3(DNA2):c.147G>T (p.Val49=)
NM_001080449.3(DNA2):c.1486T>C (p.Tyr496His)
NM_001080449.3(DNA2):c.1655C>T (p.Ser552Leu)
NM_001080449.3(DNA2):c.1943G>A (p.Gly648Asp)
NM_001080449.3(DNA2):c.2430C>G (p.Phe810Leu) rs73274785
NM_001080449.3(DNA2):c.2829C>T (p.Tyr943=)
NM_001080449.3(DNA2):c.570A>T (p.Ile190=)
NM_001080449.3(DNA2):c.720-15_720-14dup rs34191745
NM_001080449.3(DNA2):c.831T>C (p.Asp277=)
NM_001080449.3(DNA2):c.939+2T>C

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