ClinVar Miner

List of variants in gene DEPDC5 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_001242896.3(DEPDC5):c.968A>G (p.Asn323Ser) rs201776005 0.00023
NM_001242896.3(DEPDC5):c.2672G>C (p.Ser891Thr) rs185576553 0.00021
NM_001242896.3(DEPDC5):c.2066A>C (p.Glu689Ala) rs370940232 0.00011
NM_001242896.3(DEPDC5):c.3622G>A (p.Ala1208Thr) rs748662185 0.00006
NM_001242896.3(DEPDC5):c.1153C>T (p.Arg385Trp) rs200020310 0.00005
NM_001242896.3(DEPDC5):c.1226C>G (p.Thr409Arg) rs773704927 0.00004
NM_001242896.3(DEPDC5):c.501G>A (p.Thr167=) rs766360619 0.00004
NM_001242896.3(DEPDC5):c.1385A>G (p.Tyr462Cys) rs747546981 0.00001
NM_001242896.3(DEPDC5):c.1604T>C (p.Ile535Thr) rs1171016858 0.00001
NM_001242896.3(DEPDC5):c.2513G>A (p.Arg838Gln) rs1486633691 0.00001
NM_001242896.3(DEPDC5):c.274C>T (p.Pro92Ser) rs774294197 0.00001
NM_001242896.3(DEPDC5):c.3097G>T (p.Val1033Leu) rs376313159 0.00001
NM_001242896.3(DEPDC5):c.3515C>A (p.Thr1172Asn) rs865860087 0.00001
NM_001242896.3(DEPDC5):c.4019C>T (p.Ala1340Val) rs369270649 0.00001
NM_001242896.3(DEPDC5):c.4097G>A (p.Arg1366Gln) rs1064795095 0.00001
NM_001242896.3(DEPDC5):c.4571A>G (p.Gln1524Arg) rs377585542 0.00001
NM_001242896.3(DEPDC5):c.1019T>C (p.Val340Ala)
NM_001242896.3(DEPDC5):c.1122A>C (p.Leu374Phe)
NM_001242896.3(DEPDC5):c.137A>T (p.Asp46Val)
NM_001242896.3(DEPDC5):c.1403G>A (p.Arg468Lys) rs2088169081
NM_001242896.3(DEPDC5):c.1526G>A (p.Arg509His) rs372489331
NM_001242896.3(DEPDC5):c.1628A>G (p.Tyr543Cys)
NM_001242896.3(DEPDC5):c.1967C>T (p.Ala656Val) rs2089705243
NM_001242896.3(DEPDC5):c.196A>T (p.Thr66Ser) rs1556523682
NM_001242896.3(DEPDC5):c.2300A>C (p.Gln767Pro) rs1057519238
NM_001242896.3(DEPDC5):c.2416C>T (p.Arg806Cys) rs953743301
NM_001242896.3(DEPDC5):c.2500C>G (p.Pro834Ala) rs1569067813
NM_001242896.3(DEPDC5):c.2831C>T (p.Thr944Ile) rs1228740465
NM_001242896.3(DEPDC5):c.2848C>T (p.Pro950Ser)
NM_001242896.3(DEPDC5):c.3563+4A>G
NM_001242896.3(DEPDC5):c.3715C>T (p.Leu1239Phe) rs2149267051
NM_001242896.3(DEPDC5):c.3805G>A (p.Val1269Met)
NM_001242896.3(DEPDC5):c.4042G>A (p.Val1348Ile) rs1380088913
NM_001242896.3(DEPDC5):c.4058C>T (p.Thr1353Ile) rs1163140081
NM_001242896.3(DEPDC5):c.413+7A>G rs1057519230
NM_001242896.3(DEPDC5):c.414-4T>C rs2148328295
NM_001242896.3(DEPDC5):c.4189G>C (p.Val1397Leu)
NM_001242896.3(DEPDC5):c.4283G>A (p.Ser1428Asn) rs1423776421
NM_001242896.3(DEPDC5):c.4376G>A (p.Ser1459Asn) rs1245607244
NM_001242896.3(DEPDC5):c.4388A>G (p.Glu1463Gly) rs2149419608
NM_001242896.3(DEPDC5):c.461G>A (p.Gly154Asp)
NM_001242896.3(DEPDC5):c.470G>C (p.Ser157Thr)
NM_001242896.3(DEPDC5):c.608T>C (p.Leu203Pro)
NM_001242896.3(DEPDC5):c.716G>A (p.Arg239Gln) rs371511498
NM_001242896.3(DEPDC5):c.946+5G>T rs2086528141

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