ClinVar Miner

List of variants in gene DEPDC5 reported as benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP
NM_001242897.2(DEPDC5):c.1095T>C (p.Asp365=) rs79070552
NM_001242897.2(DEPDC5):c.1165C>T (p.Arg389Cys) rs41311139
NM_001242897.2(DEPDC5):c.1323A>C (p.Thr441=) rs5998135
NM_001242897.2(DEPDC5):c.1355C>T (p.Ala452Val) rs202226316
NM_001242897.2(DEPDC5):c.1472G>C (p.Ser491Thr) rs8138516
NM_001242897.2(DEPDC5):c.1870+2328C>T rs16989528
NM_001242897.2(DEPDC5):c.1870+2410A>G rs374037144
NM_001242897.2(DEPDC5):c.1870+3481C>T rs181347577
NM_001242897.2(DEPDC5):c.1870+3516C>A rs61731667
NM_001242897.2(DEPDC5):c.1901C>T (p.Ser634Phe) rs16989535
NM_001242897.2(DEPDC5):c.1905A>G (p.Leu635=) rs16989536
NM_001242897.2(DEPDC5):c.2007C>G (p.Leu669=) rs16989537
NM_001242897.2(DEPDC5):c.2247G>A (p.Pro749=) rs61731664
NM_001242897.2(DEPDC5):c.2508G>A (p.Glu836=) rs118001924
NM_001242897.2(DEPDC5):c.2622T>C (p.Cys874=) rs115299174
NM_001242897.2(DEPDC5):c.3058A>G (p.Met1020Val) rs61731662
NM_001242897.2(DEPDC5):c.4212C>T (p.His1404=) rs146449468
NM_001242897.2(DEPDC5):c.885A>G (p.Gln295=) rs16989495

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