ClinVar Miner

List of variants in gene DEPDC5 studied for not provided

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Gene type:
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Total variants: 71
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HGVS dbSNP
NM_001242896.1(DEPDC5):c.1010C>T (p.Thr337Met) rs1037878155
NM_001242896.1(DEPDC5):c.1045C>T (p.Leu349Phe) rs1085307532
NM_001242896.1(DEPDC5):c.1153C>T (p.Arg385Trp) rs200020310
NM_001242896.1(DEPDC5):c.1184A>C (p.Asp395Ala) rs1064796205
NM_001242896.1(DEPDC5):c.1247G>T (p.Cys416Phe) rs767747105
NM_001242896.1(DEPDC5):c.1290C>T (p.Pro430=) rs201202102
NM_001242896.1(DEPDC5):c.1330G>A (p.Gly444Arg) rs201394709
NM_001242896.1(DEPDC5):c.1412G>A (p.Gly471Asp) rs1351408059
NM_001242896.1(DEPDC5):c.1525C>T (p.Arg509Cys) rs202083639
NM_001242896.1(DEPDC5):c.1666G>A (p.Asp556Asn) rs1064795160
NM_001242896.1(DEPDC5):c.1898A>G (p.His633Arg) rs1064794610
NM_001242896.1(DEPDC5):c.1909C>T (p.Arg637Ter) rs780960812
NM_001242896.1(DEPDC5):c.1993G>A (p.Glu665Lys) rs753762209
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.2117G>T (p.Arg706Met) rs1064795377
NM_001242896.1(DEPDC5):c.2521G>A (p.Val841Met) rs1555899402
NM_001242896.1(DEPDC5):c.2801+8A>G rs370009456
NM_001242896.1(DEPDC5):c.2856T>C (p.Cys952=) rs115299174
NM_001242896.1(DEPDC5):c.2879C>T (p.Thr960Met) rs1064795107
NM_001242896.1(DEPDC5):c.28G>A (p.Val10Ile) rs375027042
NM_001242896.1(DEPDC5):c.3272C>T (p.Ala1091Val) rs772812141
NM_001242896.1(DEPDC5):c.3329A>G (p.Gln1110Arg) rs1555909576
NM_001242896.1(DEPDC5):c.3331-10del rs377356885
NM_001242896.1(DEPDC5):c.336_337delGG (p.Asp113Tyrfs) rs1085307452
NM_001242896.1(DEPDC5):c.3691A>G (p.Met1231Val) rs1064796392
NM_001242896.1(DEPDC5):c.380A>G (p.Tyr127Cys) rs370881336
NM_001242896.1(DEPDC5):c.3978G>T (p.Arg1326Ser) rs374647774
NM_001242896.1(DEPDC5):c.4097G>T (p.Arg1366Leu) rs1064795095
NM_001242896.1(DEPDC5):c.414-9T>G rs1556556448
NM_001242896.1(DEPDC5):c.4408C>T (p.His1470Tyr) rs1064795311
NM_001242896.1(DEPDC5):c.4504T>C (p.Tyr1502His) rs1064796662
NM_001242896.1(DEPDC5):c.4592C>T (p.Thr1531Ile) rs1064794532
NM_001242896.1(DEPDC5):c.562+1G>A rs1057524233
NM_001242896.1(DEPDC5):c.58+5G>C rs1064794917
NM_001242896.1(DEPDC5):c.59-3C>G rs1064795947
NM_001242896.1(DEPDC5):c.638G>C (p.Ser213Thr) rs374290113
NM_001242896.1(DEPDC5):c.752A>G (p.Tyr251Cys) rs1064796158
NM_001242896.1(DEPDC5):c.946+1G>A rs1556608580
NM_001242896.1(DEPDC5):c.953A>G (p.Asp318Gly) rs1064795102
NM_001242896.1(DEPDC5):c.983G>C (p.Arg328Pro) rs775605247
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.1265G>A (p.Arg422Gln) rs886039277
NM_001242896.2(DEPDC5):c.1555C>T (p.Gln519Ter) rs886039261
NM_001242896.2(DEPDC5):c.161A>C (p.Gln54Pro) rs201312113
NM_001242896.2(DEPDC5):c.1958dup (p.His653Glnfs) rs1475605360
NM_001242896.2(DEPDC5):c.2137C>A (p.Leu713Ile) rs1555894264
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.3358A>G (p.Met1120Val) rs61731662
NM_001242896.2(DEPDC5):c.388C>T (p.Gln130Ter)
NM_001242896.2(DEPDC5):c.4391C>T (p.Thr1464Met)
NM_001242896.2(DEPDC5):c.4512C>T (p.His1504=) rs146449468
NM_001242896.2(DEPDC5):c.4793T>C (p.Met1598Thr) rs1555943470
NM_001242896.2(DEPDC5):c.715C>T (p.Arg239Ter) rs587776976
NM_001242896.2(DEPDC5):c.814G>A (p.Val272Ile) rs187334123
NM_001242896.2(DEPDC5):c.842A>T (p.Tyr281Phe) rs200797928
NM_001242896.2(DEPDC5):c.856C>T (p.Arg286Ter) rs886039255
NM_001242897.1(DEPDC5):c.1226C>G (p.Thr409Arg) rs773704927
NM_001242897.1(DEPDC5):c.1474C>T (p.Arg492Ter) rs1057519107
NM_001242897.1(DEPDC5):c.1604T>C (p.Ile535Thr)
NM_001242897.1(DEPDC5):c.196A>T (p.Thr66Ser) rs1556523682
NM_001242897.1(DEPDC5):c.2066A>C (p.Gln689Pro) rs1057519238
NM_001242897.1(DEPDC5):c.2739G>A (p.Glu913=) rs370906184
NM_001242897.1(DEPDC5):c.3262_3263dup (p.Thr1089Argfs) rs1555914806
NM_001242897.1(DEPDC5):c.3797G>A (p.Arg1266Gln) rs1064795095
NM_001242897.1(DEPDC5):c.4076G>A (p.Ser1359Asn)
NM_001242897.1(DEPDC5):c.413+7A>G rs1057519230
NM_001242897.1(DEPDC5):c.4219+1G>A rs1555942720
NM_001242897.1(DEPDC5):c.501G>A (p.Thr167=) rs766360619

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