ClinVar Miner

List of variants in gene ZNF83

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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_018300.4(ZNF83):c.731G>A (p.Arg244His) rs147902645 0.00027
NM_018300.4(ZNF83):c.854G>C (p.Gly285Ala) rs146207784 0.00013
NM_018300.4(ZNF83):c.1343G>A (p.Arg448Gln) rs143220585 0.00009
NM_018300.4(ZNF83):c.922T>C (p.Trp308Arg) rs878921853 0.00008
NM_018300.4(ZNF83):c.1525G>A (p.Gly509Arg) rs142815028 0.00003
NM_018300.4(ZNF83):c.671G>A (p.Arg224Gln) rs866220340 0.00003
NM_018300.4(ZNF83):c.328A>G (p.Ile110Val) rs774411419 0.00002
NM_018300.4(ZNF83):c.1052G>A (p.Gly351Asp) rs1350614102 0.00001
NM_018300.4(ZNF83):c.1180A>C (p.Ile394Leu) rs760862058 0.00001
NM_018300.4(ZNF83):c.1420A>C (p.Asn474His) rs754974957 0.00001
NM_018300.4(ZNF83):c.1486G>A (p.Asp496Asn) rs191070309 0.00001
NM_018300.4(ZNF83):c.1493C>T (p.Ser498Leu) rs758679709 0.00001
NM_018300.4(ZNF83):c.529T>A (p.Tyr177Asn) rs199990989 0.00001
NM_018300.4(ZNF83):c.704G>A (p.Cys235Tyr) rs1366424092 0.00001
NM_018300.4(ZNF83):c.888G>C (p.Lys296Asn) rs1389895949 0.00001
NM_018300.4(ZNF83):c.1010G>A (p.Arg337Lys) rs2514499865
NM_018300.4(ZNF83):c.1067G>A (p.Arg356His)
NM_018300.4(ZNF83):c.1082C>T (p.Ala361Val)
NM_018300.4(ZNF83):c.1091T>C (p.Leu364Pro)
NM_018300.4(ZNF83):c.1094T>A (p.Ile365Lys) rs1294064240
NM_018300.4(ZNF83):c.1108G>A (p.Glu370Lys) rs1568522955
NM_018300.4(ZNF83):c.1142C>T (p.Ala381Val)
NM_018300.4(ZNF83):c.1145T>G (p.Phe382Cys)
NM_018300.4(ZNF83):c.1217G>A (p.Cys406Tyr)
NM_018300.4(ZNF83):c.1315G>A (p.Gly439Ser) rs778743816
NM_018300.4(ZNF83):c.1315G>C (p.Gly439Arg)
NM_018300.4(ZNF83):c.1406G>C (p.Arg469Pro) rs766361238
NM_018300.4(ZNF83):c.1411A>G (p.Ser471Gly)
NM_018300.4(ZNF83):c.1430C>T (p.Ala477Val) rs149457093
NM_018300.4(ZNF83):c.1459T>C (p.Cys487Arg)
NM_018300.4(ZNF83):c.163C>T (p.Pro55Ser) rs1189221087
NM_018300.4(ZNF83):c.166C>T (p.Pro56Ser)
NM_018300.4(ZNF83):c.17A>T (p.Asp6Val)
NM_018300.4(ZNF83):c.206A>G (p.His69Arg)
NM_018300.4(ZNF83):c.246A>C (p.Gln82His) rs2060230328
NM_018300.4(ZNF83):c.250G>A (p.Glu84Lys)
NM_018300.4(ZNF83):c.361T>A (p.Phe121Ile)
NM_018300.4(ZNF83):c.503G>A (p.Arg168His)
NM_018300.4(ZNF83):c.601G>A (p.Gly201Arg) rs141690119
NM_018300.4(ZNF83):c.688G>A (p.Glu230Lys) rs2060206183
NM_018300.4(ZNF83):c.70C>T (p.His24Tyr)
NM_018300.4(ZNF83):c.72T>G (p.His24Gln)
NM_018300.4(ZNF83):c.742C>A (p.Leu248Ile)
NM_018300.4(ZNF83):c.749A>G (p.Gln250Arg)
NM_018300.4(ZNF83):c.801_884del (p.His271_Phe298del) rs1568523939
NM_018300.4(ZNF83):c.824A>C (p.His275Pro) rs575275768
NM_018300.4(ZNF83):c.949T>C (p.Tyr317His)
NM_018300.4(ZNF83):c.98C>G (p.Ala33Gly) rs2514520384

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