ClinVar Miner

List of variants in gene DNA2 studied for not specified

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Gene type:
ClinVar version:
Total variants: 47
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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.1362G>A (p.Ser454=) rs74537378 0.02747
NM_001080449.3(DNA2):c.888G>A (p.Pro296=) rs16925390 0.01237
NM_001080449.3(DNA2):c.1899G>A (p.Ala633=) rs116704917 0.00869
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.2713C>A (p.Gln905Lys) rs181679245 0.00459
NM_001080449.3(DNA2):c.68C>T (p.Ala23Val) rs200467869 0.00071
NM_001080449.3(DNA2):c.2697+18T>C rs190301454 0.00040
NM_001080449.3(DNA2):c.2826G>A (p.Pro942=) rs200956547 0.00011
NM_001080449.3(DNA2):c.-21T>G rs375303446 0.00010
NM_001080449.3(DNA2):c.2706G>A (p.Ala902=) rs371684850 0.00009
NM_001080449.3(DNA2):c.1763+14A>C rs544079864 0.00007
NM_001080449.3(DNA2):c.1909G>A (p.Val637Ile) rs746522359 0.00006
NM_001080449.3(DNA2):c.1102C>T (p.Arg368Cys) rs555751651 0.00003
NM_001080449.3(DNA2):c.1116T>C (p.Ser372=) rs368778086 0.00003
NM_001080449.3(DNA2):c.2358G>A (p.Gly786=) rs773533815 0.00003
NM_001080449.3(DNA2):c.1415+16A>C rs751137634 0.00002
NM_001080449.3(DNA2):c.1485A>G (p.Gln495=) rs368855073 0.00002
NM_001080449.3(DNA2):c.3087G>A (p.Leu1029=) rs754444650 0.00001
NM_001080449.3(DNA2):c.441+15C>T rs558303170 0.00001
NC_000010.10:g.(70196999_70202673)_(70231731_?)dup
NC_000010.10:g.(?_70173820)_(70231731_?)dup
NM_001080449.3(DNA2):c.-48dup rs762749916
NM_001080449.3(DNA2):c.1057+16T>C rs1057521508
NM_001080449.3(DNA2):c.1058-13dup rs201474338
NM_001080449.3(DNA2):c.1058-6del rs201474338
NM_001080449.3(DNA2):c.1059A>T (p.Glu353Asp)
NM_001080449.3(DNA2):c.1061T>A (p.Leu354Ter) rs2133402732
NM_001080449.3(DNA2):c.1289C>T (p.Thr430Ile)
NM_001080449.3(DNA2):c.1491A>G (p.Leu497=) rs549990947
NM_001080449.3(DNA2):c.1763+12T>C
NM_001080449.3(DNA2):c.193C>T (p.Arg65Cys) rs540241779
NM_001080449.3(DNA2):c.1983+12A>C rs1057521699
NM_001080449.3(DNA2):c.2209-11C>T rs538970967
NM_001080449.3(DNA2):c.2430C>G (p.Phe810Leu) rs73274785
NM_001080449.3(DNA2):c.2697+13_2697+17delinsTT rs1064794608
NM_001080449.3(DNA2):c.2698-20C>G
NM_001080449.3(DNA2):c.52G>T (p.Glu18Ter) rs1554911818
NM_001080449.3(DNA2):c.720-9T>G
NM_001080449.3(DNA2):c.74+12G>A
NM_001080449.3(DNA2):c.74+13G>C rs370226465
NM_001080449.3(DNA2):c.74+17dup
NM_001080449.3(DNA2):c.984_985insAA (p.Glu329fs)

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