ClinVar Miner

List of variants reported as likely benign for nonpapillary renal cell carcinoma

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_000458.4(HNF1B):c.-67C>T rs140699244 0.00491
NM_000545.8(HNF1A):c.326+6_326+10dup rs56158114 0.00415
NM_144997.7(FLCN):c.1177-21G>A rs150687840 0.00276
NM_000545.8(HNF1A):c.1165T>G (p.Leu389Val) rs115080759 0.00198
NM_000458.4(HNF1B):c.951C>G (p.Ala317=) rs145750370 0.00127
NM_000545.8(HNF1A):c.1446C>T (p.Ser482=) rs147366495 0.00117
NM_000545.8(HNF1A):c.1323G>A (p.Thr441=) rs138996307 0.00081
NM_000545.8(HNF1A):c.92G>A (p.Gly31Asp) rs137853247 0.00076
NM_000551.4(VHL):c.340+578C>T rs139622356 0.00064
NM_016821.3(OGG1):c.1043G>A (p.Gly348Glu) rs41276495 0.00054
NM_144997.7(FLCN):c.1269C>T (p.His423=) rs41464156 0.00053
NM_144997.7(FLCN):c.619-20C>T rs202217257 0.00037
NM_000458.4(HNF1B):c.1207-18T>C rs199849203 0.00026
NM_144997.7(FLCN):c.1326C>T (p.His442=) rs145004158 0.00023
NM_000545.8(HNF1A):c.1386C>T (p.Val462=) rs143015301 0.00021
NM_000545.8(HNF1A):c.1108-4G>A rs372892932 0.00020
NM_000545.8(HNF1A):c.1377G>A (p.Leu459=) rs118028009 0.00020
NM_144997.7(FLCN):c.1176+15T>C rs550870270 0.00020
NM_144997.7(FLCN):c.1062+7G>A rs540198776 0.00016
NM_144997.7(FLCN):c.1278C>T (p.Ile426=) rs41459448 0.00016
NM_000458.4(HNF1B):c.1046-12G>A rs201751705 0.00014
NM_000458.4(HNF1B):c.1534+11G>A rs373875820 0.00009
NM_144997.7(FLCN):c.1432+8C>T rs201898226 0.00009
NM_144997.7(FLCN):c.779+9C>T rs373504780 0.00009
NM_000458.4(HNF1B):c.660T>C (p.Asp220=) rs779375959 0.00008
NM_144997.7(FLCN):c.792G>A (p.Ala264=) rs140500421 0.00008
NM_000458.4(HNF1B):c.1534+10C>T rs368168569 0.00007
NM_144997.7(FLCN):c.867C>T (p.Leu289=) rs367562964 0.00007
NM_000545.8(HNF1A):c.1071G>A (p.Glu357=) rs376279459 0.00006
NM_144997.7(FLCN):c.396+7C>T rs781155484 0.00006
NM_144997.7(FLCN):c.1692C>T (p.His564=) rs201810397 0.00005
NM_000458.4(HNF1B):c.723G>A (p.Ala241=) rs768490293 0.00004
NM_000545.8(HNF1A):c.1015G>A (p.Gly339Ser) rs766790596 0.00004
NM_000545.8(HNF1A):c.150C>T (p.Cys50=) rs193922583 0.00004
NM_000545.8(HNF1A):c.713+13G>A rs755961371 0.00004
NM_000551.4(VHL):c.420C>A (p.Leu140=) rs369465430 0.00004
NM_144997.7(FLCN):c.1068G>T (p.Leu356=) rs534904034 0.00004
NM_144997.7(FLCN):c.645C>T (p.Cys215=) rs772360950 0.00004
NM_144997.7(FLCN):c.1380C>T (p.Leu460=) rs773581294 0.00003
NM_144997.7(FLCN):c.450T>C (p.Phe150=) rs200672897 0.00003
NM_000551.4(VHL):c.267C>A (p.Leu89=) rs755794553 0.00002
NM_000545.8(HNF1A):c.153C>T (p.Gly51=) rs761779651 0.00001
NM_000545.8(HNF1A):c.685C>A (p.Arg229=) rs769086289 0.00001
NM_000551.4(VHL):c.426T>C (p.Val142=) rs143594610 0.00001
NM_144997.7(FLCN):c.1227C>T (p.Tyr409=) rs561236067 0.00001
NM_144997.7(FLCN):c.1301-8T>C rs571192457 0.00001
NM_144997.7(FLCN):c.1539-11G>C rs368472222 0.00001
NM_144997.7(FLCN):c.619-8C>T rs1274815686 0.00001
NM_144997.7(FLCN):c.780-13C>T rs777670469 0.00001
NM_144997.7(FLCN):c.981A>G (p.Ala327=) rs763078516 0.00001
NM_000458.4(HNF1B):c.1474G>A (p.Gly492Ser)
NM_000458.4(HNF1B):c.226G>T (p.Gly76Cys)
NM_000458.4(HNF1B):c.544+14T>A rs759120365
NM_000458.4(HNF1B):c.657C>T (p.Ser219=) rs148713761
NM_000458.4(HNF1B):c.831G>A (p.Gly277=) rs199797518
NM_000545.8(HNF1A):c.-167TGGGGGT[3] rs538476099
NM_000545.8(HNF1A):c.1719_1720inv (p.Ser574Gly)
NM_000545.8(HNF1A):c.498C>T (p.Tyr166=) rs1876675633
NM_000551.4(VHL):c.-10C>T rs1192379474
NM_000551.4(VHL):c.463+9G>A rs1057522720
NM_144997.7(FLCN):c.1353T>C (p.Pro451=) rs1597580172
NM_144997.7(FLCN):c.756G>A (p.Ala252=) rs746664975
NM_144997.7(FLCN):c.871+13T>C rs770537219

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