ClinVar Miner

List of variants in gene CDK13 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_003718.5(CDK13):c.3508G>A (p.Val1170Met) rs3204309 0.00488
NM_003718.5(CDK13):c.2009C>G (p.Thr670Arg) rs34775357 0.00460
NM_003718.5(CDK13):c.2124C>T (p.Ile708=) rs142726395 0.00360
NM_003718.5(CDK13):c.1066C>G (p.Pro356Ala) rs17537669 0.00258
NM_003718.5(CDK13):c.2985C>T (p.Cys995=) rs56028037 0.00218
NM_003718.5(CDK13):c.642C>T (p.Arg214=) rs143271914 0.00186
NM_003718.5(CDK13):c.1260A>G (p.Ser420=) rs139746338 0.00135
NM_003718.5(CDK13):c.4266C>T (p.Asp1422=) rs139981763 0.00024
NM_003718.5(CDK13):c.1242G>A (p.Pro414=) rs202080779 0.00013
NM_003718.5(CDK13):c.1462A>G (p.Lys488Glu) rs780866053 0.00005
NM_003718.5(CDK13):c.1401C>T (p.Ala467=) rs137937704 0.00003
NM_003718.5(CDK13):c.3737C>T (p.Thr1246Met) rs761120542 0.00001
NM_003718.5(CDK13):c.1023C>T (p.Pro341=)
NM_003718.5(CDK13):c.132G>A (p.Leu44=)
NM_003718.5(CDK13):c.1408G>A (p.Ala470Thr)
NM_003718.5(CDK13):c.144C>T (p.Leu48=)
NM_003718.5(CDK13):c.1555A>G (p.Lys519Glu) rs2116266403
NM_003718.5(CDK13):c.1644G>A (p.Val548=)
NM_003718.5(CDK13):c.1871+6T>C
NM_003718.5(CDK13):c.2068A>G (p.Thr690Ala)
NM_003718.5(CDK13):c.2181T>G (p.Thr727=)
NM_003718.5(CDK13):c.2235T>C (p.Phe745=)
NM_003718.5(CDK13):c.2412A>G (p.Ser804=)
NM_003718.5(CDK13):c.2600+4936_2600+4938del
NM_003718.5(CDK13):c.3258C>G (p.His1086Gln)
NM_003718.5(CDK13):c.3502C>T (p.Pro1168Ser)
NM_003718.5(CDK13):c.3530C>T (p.Ala1177Val)
NM_003718.5(CDK13):c.3758G>A (p.Arg1253Gln) rs150957134
NM_003718.5(CDK13):c.3888C>T (p.Ala1296=) rs150235453
NM_003718.5(CDK13):c.4121T>C (p.Ile1374Thr)
NM_003718.5(CDK13):c.4444A>C (p.Thr1482Pro)
NM_003718.5(CDK13):c.4461A>G (p.Gly1487=)
NM_003718.5(CDK13):c.45G>A (p.Leu15=)
NM_003718.5(CDK13):c.501G>A (p.Ala167=)
NM_003718.5(CDK13):c.657G>A (p.Arg219=)
NM_003718.5(CDK13):c.729C>G (p.Ala243=)
NM_003718.5(CDK13):c.741G>A (p.Lys247=)
NM_003718.5(CDK13):c.867G>A (p.Pro289=)
NM_003718.5(CDK13):c.869C>T (p.Pro290Leu) rs923708985
NM_003718.5(CDK13):c.955C>T (p.Leu319=)

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