ClinVar Miner

List of variants in gene ZNF711 studied for X-linked disease

Included ClinVar conditions (275):
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Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_001330574.2(ZNF711):c.-286+5C>T rs41311563 0.22093
NM_001330574.2(ZNF711):c.*153A>G rs2343388 0.21897
NM_001330574.2(ZNF711):c.-449A>G rs375972814 0.03298
NM_001330574.2(ZNF711):c.798A>G (p.Thr266=) rs72549428 0.01228
NM_001330574.2(ZNF711):c.-297A>T rs772828408 0.00370
NM_001330574.2(ZNF711):c.*122G>T rs755444976 0.00218
NM_001330574.2(ZNF711):c.*540T>C rs761918833 0.00212
NM_001330574.2(ZNF711):c.829G>A (p.Ala277Thr) rs145361311 0.00123
NM_001330574.2(ZNF711):c.2106A>G (p.Thr702=) rs138675194 0.00097
NM_001330574.2(ZNF711):c.*763G>A rs779266566 0.00071
NM_001330574.2(ZNF711):c.*118C>T rs907642064 0.00059
NM_001330574.2(ZNF711):c.*272G>A rs187954106 0.00055
NM_001330574.2(ZNF711):c.1464C>T (p.Val488=) rs140843429 0.00034
NM_001330574.2(ZNF711):c.-316T>A rs760150680 0.00031
NM_001330574.2(ZNF711):c.*169C>T rs748560628 0.00017
NM_001330574.2(ZNF711):c.326G>C (p.Gly109Ala) rs769223012 0.00005
NM_001330574.2(ZNF711):c.1940A>G (p.Asn647Ser) rs760346140 0.00003
NM_001330574.2(ZNF711):c.1773A>G (p.Gln591=) rs370054764 0.00002
NM_001330574.2(ZNF711):c.1926C>A (p.Asp642Glu) rs780662376 0.00002
NM_001330574.2(ZNF711):c.*47A>G rs755503652 0.00001
NM_001330574.2(ZNF711):c.2109C>T (p.Ser703=) rs150030676 0.00001
NM_001330574.2(ZNF711):c.2173A>G (p.Lys725Glu) rs367944400 0.00001
NM_001330574.2(ZNF711):c.61A>G (p.Met21Val) rs1381801436 0.00001
NM_001330574.2(ZNF711):c.*188A>G rs1057516016
NM_001330574.2(ZNF711):c.*524C>T rs1931629284
NM_001330574.2(ZNF711):c.*965T>A rs1931660931
NM_001330574.2(ZNF711):c.-350G>T rs1057516013
NM_001330574.2(ZNF711):c.-439dup rs1057516012
NM_001330574.2(ZNF711):c.-449delinsGGCGGCGGCG rs1057516011
NM_001330574.2(ZNF711):c.-458_-438del
NM_001330574.2(ZNF711):c.-473GGC[10] rs758475553
NM_001330574.2(ZNF711):c.-473GGC[9] rs758475553
NM_001330574.2(ZNF711):c.1068_1069del (p.Arg356fs) rs1931281945
NM_001330574.2(ZNF711):c.1073C>G (p.Ser358Cys) rs1931282299
NM_001330574.2(ZNF711):c.124GTT[1] (p.Val43del) rs587780527
NM_001330574.2(ZNF711):c.125T>G (p.Val42Gly)
NM_001330574.2(ZNF711):c.1368G>A (p.Met456Ile) rs200444579
NM_001330574.2(ZNF711):c.1377dup (p.Tyr460fs) rs1555974716
NM_001330574.2(ZNF711):c.1379A>T (p.Tyr460Phe) rs2147874862
NM_001330574.2(ZNF711):c.1711A>T (p.Arg571Ter) rs199422240
NM_001330574.2(ZNF711):c.1761G>T (p.Arg587Ser)
NM_001330574.2(ZNF711):c.1877A>G (p.His626Arg) rs2147876365
NM_001330574.2(ZNF711):c.1882G>A (p.Asp628Asn) rs1426575922
NM_001330574.2(ZNF711):c.2162C>T (p.Pro721Leu) rs1057516014
NM_001330574.2(ZNF711):c.2192del (p.Phe731fs) rs1060505032
NM_001330574.2(ZNF711):c.2210T>G (p.Leu737Arg) rs1555975302
NM_001330574.2(ZNF711):c.2217del (p.Lys739fs)
NM_001330574.2(ZNF711):c.2265_2266del (p.Cys755_Glu756delinsTer) rs1603009115
NM_001330574.2(ZNF711):c.321T>A (p.Asp107Glu) rs1292116347
NM_001330574.2(ZNF711):c.416G>A (p.Gly139Glu)
NM_001330574.2(ZNF711):c.569ATG[5] (p.Asp195del) rs746649683
NM_001330574.2(ZNF711):c.731T>C (p.Ile244Thr) rs1060505033
NM_001330574.2(ZNF711):c.900AGA[2] (p.Glu302del)
NM_001330574.2(ZNF711):c.97dup (p.Thr33fs) rs1555970404

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