ClinVar Miner

List of variants in gene RET reported by Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden

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Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.166C>A (p.Leu56Met) rs145633958 0.00310
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala) rs201740483 0.00047
NM_020975.6(RET):c.1946C>T (p.Ser649Leu) rs148935214 0.00039
NM_020975.6(RET):c.874G>A (p.Val292Met) rs34682185 0.00023
NM_020975.6(RET):c.2657G>A (p.Arg886Gln) rs373594744 0.00009
NM_020975.6(RET):c.961G>A (p.Gly321Arg) rs377767388 0.00009
NM_020975.6(RET):c.1894G>A (p.Glu632Lys) rs377767407 0.00006
NM_020975.6(RET):c.224C>T (p.Thr75Met) rs142641173 0.00006
NM_020975.6(RET):c.2527G>A (p.Glu843Lys) rs755837568 0.00006
NM_020975.6(RET):c.2940-26A>C rs752405055 0.00004
NM_020975.6(RET):c.3094G>A (p.Gly1032Ser) rs757373375 0.00004
NM_020975.6(RET):c.322A>C (p.Lys108Gln) rs567877611 0.00004
NM_020975.6(RET):c.3253A>G (p.Thr1085Ala) rs756465544 0.00004
NM_020975.6(RET):c.1686C>T (p.Thr562=) rs767502292 0.00001
NM_020975.6(RET):c.2370G>T (p.Leu790Phe) rs75030001 0.00001
NM_020975.6(RET):c.1349G>T (p.Ser450Ile) rs2132768628
NM_020975.6(RET):c.1901G>T (p.Cys634Phe) rs75996173
NM_020975.6(RET):c.1995C>A (p.His665Gln) rs377767413
NM_020975.6(RET):c.867+9C>T rs2132709396

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