ClinVar Miner

List of variants reported as likely benign for Renal cell carcinoma, papillary, 1 by Invitae

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ClinVar version:
Total variants: 33
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HGVS dbSNP
NM_001127500.3(MET):c.-7T>C rs863224376
NM_001127500.3(MET):c.1365T>G (p.Leu455=) rs369639118
NM_001127500.3(MET):c.141C>G (p.Thr47=) rs864622222
NM_001127500.3(MET):c.1485A>G (p.Thr495=) rs760256871
NM_001127500.3(MET):c.1528-9T>C rs767768257
NM_001127500.3(MET):c.1602C>A (p.Pro534=) rs1554391268
NM_001127500.3(MET):c.1641A>C (p.Arg547=) rs1554391313
NM_001127500.3(MET):c.1665A>G (p.Thr555=) rs1554391336
NM_001127500.3(MET):c.1702-8C>T rs1554394916
NM_001127500.3(MET):c.1812C>T (p.Leu604=) rs1412870024
NM_001127500.3(MET):c.1881T>G (p.Gly627=) rs200050499
NM_001127500.3(MET):c.2073A>G (p.Ser691=) rs765318603
NM_001127500.3(MET):c.2220A>G (p.Glu740=) rs1554395720
NM_001127500.3(MET):c.2232C>G (p.Val744=) rs1060504944
NM_001127500.3(MET):c.2304A>C (p.Leu768=) rs201304108
NM_001127500.3(MET):c.2391G>A (p.Val797=) rs863224377
NM_001127500.3(MET):c.2638-8C>G rs370833501
NM_001127500.3(MET):c.2772G>A (p.Glu924=) rs752013993
NM_001127500.3(MET):c.2814T>C (p.Leu938=) rs1554398258
NM_001127500.3(MET):c.2823A>C (p.Val941=) rs371015065
NM_001127500.3(MET):c.3097T>G (p.Ser1033Ala) rs539345989
NM_001127500.3(MET):c.3285T>A (p.Ile1095=) rs1251215478
NM_001127500.3(MET):c.3354T>C (p.Asn1118=) rs1554399341
NM_001127500.3(MET):c.3399C>T (p.Ile1133=) rs1554399534
NM_001127500.3(MET):c.3577-6C>T rs1554400069
NM_001127500.3(MET):c.3870C>A (p.Leu1290=) rs757012119
NM_001127500.3(MET):c.3921C>T (p.Thr1307=) rs587780532
NM_001127500.3(MET):c.3924T>C (p.Phe1308=) rs926365001
NM_001127500.3(MET):c.4128C>T (p.Asn1376=) rs772860611
NM_001127500.3(MET):c.669A>G (p.Lys223=) rs863224380
NM_001127500.3(MET):c.690G>T (p.Thr230=) rs200138253
NM_001127500.3(MET):c.813T>C (p.Ala271=) rs750586651
NM_001127500.3(MET):c.912A>G (p.Arg304=) rs762885066

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