ClinVar Miner

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

Included ClinVar conditions (313):
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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_001330574.2(ZNF711):c.*118C>T rs907642064
NM_001330574.2(ZNF711):c.*122G>T rs755444976
NM_001330574.2(ZNF711):c.*153A>G rs2343388
NM_001330574.2(ZNF711):c.*169C>T
NM_001330574.2(ZNF711):c.*188A>G rs1057516016
NM_001330574.2(ZNF711):c.*272G>A rs187954106
NM_001330574.2(ZNF711):c.*47A>G rs755503652
NM_001330574.2(ZNF711):c.*524C>T
NM_001330574.2(ZNF711):c.*540T>C rs761918833
NM_001330574.2(ZNF711):c.*763G>A rs779266566
NM_001330574.2(ZNF711):c.*965T>A
NM_001330574.2(ZNF711):c.-286+5C>T rs41311563
NM_001330574.2(ZNF711):c.-297A>T
NM_001330574.2(ZNF711):c.-316T>A rs760150680
NM_001330574.2(ZNF711):c.-350G>T rs1057516013
NM_001330574.2(ZNF711):c.-449A>G rs375972814
NM_001330574.2(ZNF711):c.1073C>G (p.Ser358Cys)
NM_001330574.2(ZNF711):c.1368G>A (p.Met456Ile) rs200444579
NM_001330574.2(ZNF711):c.1464C>T (p.Val488=) rs140843429
NM_001330574.2(ZNF711):c.1773A>G (p.Gln591=)
NM_001330574.2(ZNF711):c.1926C>A (p.Asp642Glu)
NM_001330574.2(ZNF711):c.2106A>G (p.Thr702=) rs138675194
NM_001330574.2(ZNF711):c.2109C>T (p.Ser703=)
NM_001330574.2(ZNF711):c.2162C>T (p.Pro721Leu) rs1057516014
NM_001330574.2(ZNF711):c.2263_2264TG[1] (p.Cys755_Glu756delinsTer) rs1603009115
NM_001330574.2(ZNF711):c.731T>C (p.Ile244Thr) rs1060505033
NM_001330574.2(ZNF711):c.798A>G (p.Thr266=) rs72549428
NM_001330574.2(ZNF711):c.829G>A (p.Ala277Thr) rs145361311
NM_021998.5(ZNF711):c.-180dup rs1057516012
NM_021998.5(ZNF711):c.-190delinsGGCGGCGGCG rs1057516011
NM_021998.5(ZNF711):c.-214_-212GGC[10] rs758475553
NM_021998.5(ZNF711):c.-214_-212GGC[9] rs758475553
NM_021998.5(ZNF711):c.1239dup (p.Tyr414fs) rs1555974716
NM_021998.5(ZNF711):c.1573A>T (p.Arg525Ter) rs199422240
NM_021998.5(ZNF711):c.2054del (p.Phe685fs) rs1060505032
NM_021998.5(ZNF711):c.2072T>G (p.Leu691Arg) rs1555975302
NM_021998.5(ZNF711):c.326G>C (p.Gly109Ala) rs769223012
NM_021998.5(ZNF711):c.97dup (p.Thr33fs) rs1555970404

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