ClinVar Miner

List of variants reported as uncertain significance for Renal cell carcinoma, papillary, 1 by Illumina Clinical Services Laboratory,Illumina

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Total variants: 31
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HGVS dbSNP
NM_001127500.3(MET):c.*105C>A rs886061945
NM_001127500.3(MET):c.*1460C>G rs886061949
NM_001127500.3(MET):c.*1593G>A rs764929802
NM_001127500.3(MET):c.*1809C>T rs868554436
NM_001127500.3(MET):c.*1882G>T rs886061950
NM_001127500.3(MET):c.*2051C>T rs886061951
NM_001127500.3(MET):c.*2079G>A rs757859772
NM_001127500.3(MET):c.*221G>A rs886061946
NM_001127500.3(MET):c.*41A>G rs771518812
NM_001127500.3(MET):c.*422T>A rs886061947
NM_001127500.3(MET):c.*995G>T rs886061948
NM_001127500.3(MET):c.-157T>G rs886061940
NM_001127500.3(MET):c.-165C>G rs886061939
NM_001127500.3(MET):c.-180C>A rs886061938
NM_001127500.3(MET):c.-64G>T rs866509744
NM_001127500.3(MET):c.-66G>T rs886061941
NM_001127500.3(MET):c.1011G>A (p.Leu337=) rs886061942
NM_001127500.3(MET):c.1174C>A (p.Pro392Thr) rs886061943
NM_001127500.3(MET):c.12C>T (p.Pro4=) rs772251895
NM_001127500.3(MET):c.1320A>G (p.Thr440=) rs763726060
NM_001127500.3(MET):c.1412G>A (p.Gly471Glu) rs373312981
NM_001127500.3(MET):c.1484C>G (p.Thr495Arg) rs45585831
NM_001127500.3(MET):c.1669A>G (p.Thr557Ala) rs374733251
NM_001127500.3(MET):c.1693A>G (p.Ile565Val) rs745479104
NM_001127500.3(MET):c.1863-5dup rs766900241
NM_001127500.3(MET):c.1965+11T>G rs780230492
NM_001127500.3(MET):c.1972G>A (p.Val658Ile) rs587778446
NM_001127500.3(MET):c.2419-14G>T rs769247886
NM_001127500.3(MET):c.4128C>T (p.Asn1376=) rs772860611
NM_001127500.3(MET):c.4129G>A (p.Val1377Ile) rs752669237
NM_001127500.3(MET):c.639G>A (p.Ser213=) rs587780738

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