ClinVar Miner

List of variants studied for Renal cell carcinoma, papillary, 1 by Mendelics

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ClinVar version:
Total variants: 80
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HGVS dbSNP
NM_001127500.3(MET):c.100G>A (p.Glu34Lys) rs764246939
NM_001127500.3(MET):c.1039G>A (p.Ala347Thr) rs200074800
NM_001127500.3(MET):c.103A>T (p.Met35Leu) rs375353223
NM_001127500.3(MET):c.1076G>A (p.Arg359Gln) rs201274041
NM_001127500.3(MET):c.110T>C (p.Val37Ala) rs201315884
NM_001127500.3(MET):c.1125C>G (p.Asn375Lys) rs776693512
NM_001127500.3(MET):c.1171G>A (p.Gly391Arg) rs587778443
NM_001127500.3(MET):c.1238G>A (p.Arg413His) rs375391602
NM_001127500.3(MET):c.1306G>A (p.Glu436Lys) rs200740468
NM_001127500.3(MET):c.135C>G (p.Asn45Lys) rs1562883006
NM_001127500.3(MET):c.1393-1G>T
NM_001127500.3(MET):c.1393-2A>T
NM_001127500.3(MET):c.1444G>A (p.Asp482Asn) rs863224694
NM_001127500.3(MET):c.1451A>G (p.His484Arg) rs781545528
NM_001127500.3(MET):c.1496A>G (p.Asn499Ser) rs1253878709
NM_001127500.3(MET):c.1508T>A (p.Leu503Gln) rs1562908826
NM_001127500.3(MET):c.1640G>A (p.Arg547Gln) rs761951444
NM_001127500.3(MET):c.1701+58dup
NM_001127500.3(MET):c.1701+59G>T
NM_001127500.3(MET):c.1715G>A (p.Ser572Asn) rs199771406
NM_001127500.3(MET):c.1771C>T (p.Arg591Trp) rs45602940
NM_001127500.3(MET):c.1866G>C (p.Leu622Phe) rs1562921668
NM_001127500.3(MET):c.1904A>G (p.Asn635Ser) rs773826297
NM_001127500.3(MET):c.1933G>A (p.Gly645Arg) rs763849125
NM_001127500.3(MET):c.1973T>C (p.Val658Ala)
NM_001127500.3(MET):c.1988C>T (p.Ser663Leu) rs376459715
NM_001127500.3(MET):c.2102+7T>C
NM_001127500.3(MET):c.2103-1G>T rs1336351205
NM_001127500.3(MET):c.2103-2A>T
NM_001127500.3(MET):c.215T>C (p.Val72Ala) rs973796037
NM_001127500.3(MET):c.2192G>A (p.Arg731Gln) rs45446492
NM_001127500.3(MET):c.236A>G (p.Gln79Arg) rs1562883214
NM_001127500.3(MET):c.2372C>T (p.Pro791Leu) rs771333219
NM_001127500.3(MET):c.2419-21G>C
NM_001127500.3(MET):c.252C>T (p.Tyr84=)
NM_001127500.3(MET):c.2622T>G (p.Asn874Lys) rs118057172
NM_001127500.3(MET):c.2638-1G>T
NM_001127500.3(MET):c.2638-3C>T rs1337305891
NM_001127500.3(MET):c.2638-9del
NM_001127500.3(MET):c.2726C>G (p.Ala909Gly) rs1562929174
NM_001127500.3(MET):c.2769C>T (p.Ser923=) rs45572835
NM_001127500.3(MET):c.2770G>A (p.Glu924Lys) rs778115147
NM_001127500.3(MET):c.2879C>T (p.Ser960Leu) rs375576430
NM_001127500.3(MET):c.2941+5A>T rs752292538
NM_001127500.3(MET):c.2946G>A (p.Leu982=)
NM_001127500.3(MET):c.2962C>T (p.Arg988Cys) rs34589476
NM_001127500.3(MET):c.3029C>T (p.Thr1010Ile) rs56391007
NM_001127500.3(MET):c.3049G>C (p.Glu1017Gln) rs1404824650
NM_001127500.3(MET):c.305G>A (p.Ser102Asn) rs779897466
NM_001127500.3(MET):c.3272C>T (p.Pro1091Leu) rs370529693
NM_001127500.3(MET):c.3328G>A (p.Val1110Ile) rs786202724
NM_001127500.3(MET):c.3406A>G (p.Ile1136Val) rs755234697
NM_001127500.3(MET):c.3410G>C (p.Gly1137Ala) rs201037977
NM_001127500.3(MET):c.362T>C (p.Val121Ala) rs879254339
NM_001127500.3(MET):c.3686+42C>G
NM_001127500.3(MET):c.3932C>G (p.Thr1311Ser) rs779121848
NM_001127500.3(MET):c.4045T>G (p.Ser1349Ala) rs1562941559
NM_001127500.3(MET):c.4061G>A (p.Arg1354Gln) rs369312680
NM_001127500.3(MET):c.406G>A (p.Val136Ile) rs199701987
NM_001127500.3(MET):c.4095G>T (p.Glu1365Asp) rs1562941622
NM_001127500.3(MET):c.40C>T (p.Leu14Phe) rs763344951
NM_001127500.3(MET):c.410A>G (p.Asn137Ser)
NM_001127500.3(MET):c.4141G>A (p.Ala1381Thr) rs45578433
NM_001127500.3(MET):c.4154C>G (p.Ser1385Cys) rs747239403
NM_001127500.3(MET):c.4194C>A (p.Asp1398Glu)
NM_001127500.3(MET):c.428G>A (p.Arg143Gln) rs35469582
NM_001127500.3(MET):c.465G>T (p.Gln155His) rs863224695
NM_001127500.3(MET):c.467C>T (p.Ser156Leu) rs56311081
NM_001127500.3(MET):c.504G>T (p.Glu168Asp) rs55985569
NM_001127500.3(MET):c.569A>G (p.Asp190Gly) rs1028165414
NM_001127500.3(MET):c.71G>A (p.Gly24Glu) rs180985111
NM_001127500.3(MET):c.728A>G (p.Asp243Gly) rs1562883992
NM_001127500.3(MET):c.789G>A (p.Thr263=) rs554190225
NM_001127500.3(MET):c.803C>T (p.Thr268Ile) rs757427533
NM_001127500.3(MET):c.850A>G (p.Ile284Val) rs776014448
NM_001127500.3(MET):c.925A>C (p.Thr309Pro) rs35601148
NM_001127500.3(MET):c.959C>T (p.Ala320Val) rs35776110
NM_001127500.3(MET):c.967A>G (p.Ser323Gly) rs201467281
NM_004958.4(MTOR):c.3026G>A (p.Arg1009Gln)
NM_004958.4(MTOR):c.889G>A (p.Asp297Asn)

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