ClinVar Miner

List of variants in gene DEPDC5 reported as benign for Epilepsy, familial focal, with variable foci 1

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Total variants: 30
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HGVS dbSNP
NM_001242896.1(DEPDC5):c.1389C>T (p.Asp463=) rs188147862
NM_001242896.1(DEPDC5):c.1472G>C (p.Ser491Thr) rs8138516
NM_001242896.1(DEPDC5):c.1922C>T (p.Ala641Val) rs16989528
NM_001242896.1(DEPDC5):c.2004A>G (p.Gly668=) rs374037144
NM_001242896.1(DEPDC5):c.2020C>T (p.Arg674Cys) rs181347577
NM_001242896.1(DEPDC5):c.2055C>A (p.Phe685Leu) rs61731667
NM_001242896.1(DEPDC5):c.2072T>C (p.Leu691Pro) rs201464790
NM_001242896.1(DEPDC5):c.2075C>T (p.Ser692Phe) rs199783404
NM_001242896.1(DEPDC5):c.2135C>T (p.Ser712Phe) rs16989535
NM_001242896.1(DEPDC5):c.2139A>G (p.Leu713=) rs16989536
NM_001242896.1(DEPDC5):c.2241C>G (p.Leu747=) rs16989537
NM_001242896.1(DEPDC5):c.2801+8A>G rs370009456
NM_001242896.1(DEPDC5):c.2856T>C (p.Cys952=) rs115299174
NM_001242896.1(DEPDC5):c.3567A>G (p.Thr1189=) rs142197878
NM_001242896.1(DEPDC5):c.364-10C>T rs116263417
NM_001242896.1(DEPDC5):c.3643G>A (p.Val1215Met) rs201603222
NM_001242896.1(DEPDC5):c.3683T>C (p.Ile1228Thr) rs200653339
NM_001242896.1(DEPDC5):c.3810C>T (p.Ala1270=) rs200033252
NM_001242896.1(DEPDC5):c.4302C>G (p.Pro1434=) rs531253840
NM_001242896.2(DEPDC5):c.1095T>C (p.Asp365=) rs79070552
NM_001242896.2(DEPDC5):c.1165C>T (p.Arg389Cys) rs41311139
NM_001242896.2(DEPDC5):c.1355C>T (p.Ala452Val) rs202226316
NM_001242896.2(DEPDC5):c.161A>C (p.Gln54Pro) rs201312113
NM_001242896.2(DEPDC5):c.2286C>T (p.Asp762=) rs200465447
NM_001242896.2(DEPDC5):c.2481G>A (p.Pro827=) rs61731664
NM_001242896.2(DEPDC5):c.2742G>A (p.Glu914=) rs118001924
NM_001242896.2(DEPDC5):c.3358A>G (p.Met1120Val) rs61731662
NM_001242896.2(DEPDC5):c.4512C>T (p.His1504=) rs146449468
NM_001242896.2(DEPDC5):c.814G>A (p.Val272Ile) rs187334123
NM_001242896.2(DEPDC5):c.885A>G (p.Gln295=) rs16989495

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