ClinVar Miner

List of variants in gene GEMIN4 reported as uncertain significance for not specified

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Gene type:
ClinVar version:
Total variants: 126
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HGVS dbSNP gnomAD frequency
NM_015721.3(GEMIN4):c.2218G>A (p.Val740Ile) rs201418426 0.00021
NM_015721.3(GEMIN4):c.3068G>A (p.Ser1023Asn) rs200379895 0.00021
NM_015721.3(GEMIN4):c.2864G>A (p.Arg955Lys) rs372573642 0.00017
NM_015721.3(GEMIN4):c.2156G>A (p.Arg719Gln) rs368956857 0.00016
NM_015721.3(GEMIN4):c.253C>T (p.Pro85Ser) rs146489979 0.00011
NM_015721.3(GEMIN4):c.1048G>A (p.Asp350Asn) rs373067107 0.00010
NM_015721.3(GEMIN4):c.1636G>A (p.Val546Met) rs776878928 0.00010
NM_015721.3(GEMIN4):c.1966G>T (p.Val656Phe) rs200818121 0.00009
NM_015721.3(GEMIN4):c.2956G>C (p.Ala986Pro) rs368556925 0.00008
NM_015721.3(GEMIN4):c.1249C>T (p.Arg417Cys) rs370614163 0.00007
NM_015721.3(GEMIN4):c.1739A>C (p.Gln580Pro) rs143008523 0.00007
NM_015721.3(GEMIN4):c.559C>T (p.His187Tyr) rs370890294 0.00006
NM_015721.3(GEMIN4):c.803A>G (p.Lys268Arg) rs745658514 0.00006
NM_015721.3(GEMIN4):c.1502G>T (p.Gly501Val) rs373006908 0.00005
NM_015721.3(GEMIN4):c.3139C>T (p.Arg1047Trp) rs373429888 0.00005
NM_015721.3(GEMIN4):c.625G>A (p.Ala209Thr) rs574847303 0.00005
NM_015721.3(GEMIN4):c.1429C>T (p.Arg477Trp) rs375394486 0.00004
NM_015721.3(GEMIN4):c.2441G>A (p.Gly814Glu) rs762179903 0.00004
NM_015721.3(GEMIN4):c.2612G>A (p.Arg871His) rs755795802 0.00004
NM_015721.3(GEMIN4):c.1394G>A (p.Ser465Asn) rs373164512 0.00003
NM_015721.3(GEMIN4):c.1589T>G (p.Phe530Cys) rs373738849 0.00003
NM_015721.3(GEMIN4):c.1596G>C (p.Gln532His) rs755795720 0.00003
NM_015721.3(GEMIN4):c.164C>T (p.Ser55Leu) rs375811017 0.00003
NM_015721.3(GEMIN4):c.1831G>A (p.Val611Ile) rs368058625 0.00003
NM_015721.3(GEMIN4):c.2618A>G (p.His873Arg) rs747727109 0.00003
NM_015721.3(GEMIN4):c.271C>T (p.Arg91Trp) rs763067962 0.00003
NM_015721.3(GEMIN4):c.2924C>A (p.Ala975Asp) rs549075664 0.00003
NM_015721.3(GEMIN4):c.650C>T (p.Ala217Val) rs968014356 0.00003
NM_015721.3(GEMIN4):c.652A>G (p.Met218Val) rs369253676 0.00003
NM_015721.3(GEMIN4):c.716C>T (p.Ala239Val) rs371494814 0.00003
NM_015721.3(GEMIN4):c.887C>A (p.Ala296Glu) rs765568374 0.00003
NM_015721.3(GEMIN4):c.1335G>C (p.Arg445Ser) rs558481262 0.00002
NM_015721.3(GEMIN4):c.2243C>T (p.Ser748Phe) rs1974376962 0.00002
NM_015721.3(GEMIN4):c.340G>A (p.Glu114Lys) rs530471988 0.00002
NM_015721.3(GEMIN4):c.381G>C (p.Gln127His) rs200790925 0.00002
NM_015721.3(GEMIN4):c.833C>T (p.Ser278Leu) rs369915879 0.00002
NM_015721.3(GEMIN4):c.1076C>T (p.Ala359Val) rs746868972 0.00001
NM_015721.3(GEMIN4):c.1079C>T (p.Thr360Met) rs771449444 0.00001
NM_015721.3(GEMIN4):c.130C>T (p.Arg44Trp) rs374771685 0.00001
NM_015721.3(GEMIN4):c.1372C>G (p.Leu458Val) rs2544542122 0.00001
NM_015721.3(GEMIN4):c.1715T>G (p.Leu572Arg) rs775642910 0.00001
NM_015721.3(GEMIN4):c.2018T>G (p.Ile673Ser) rs1232319633 0.00001
NM_015721.3(GEMIN4):c.2164T>C (p.Ser722Pro) rs754909003 0.00001
NM_015721.3(GEMIN4):c.2267T>G (p.Leu756Arg) rs1237058103 0.00001
NM_015721.3(GEMIN4):c.2335G>A (p.Glu779Lys) rs763098397 0.00001
NM_015721.3(GEMIN4):c.2474C>A (p.Ser825Tyr) rs778534939 0.00001
NM_015721.3(GEMIN4):c.247G>A (p.Val83Met) rs778610719 0.00001
NM_015721.3(GEMIN4):c.2533G>A (p.Glu845Lys) rs200154639 0.00001
NM_015721.3(GEMIN4):c.2699T>G (p.Leu900Arg) rs1974352455 0.00001
NM_015721.3(GEMIN4):c.2935T>C (p.Tyr979His) rs761766279 0.00001
NM_015721.3(GEMIN4):c.3143G>A (p.Arg1048His) rs746141568 0.00001
NM_015721.3(GEMIN4):c.433C>A (p.Leu145Met) rs775748616 0.00001
NM_015721.3(GEMIN4):c.665G>A (p.Gly222Glu) rs763015485 0.00001
NM_015721.3(GEMIN4):c.727C>G (p.Leu243Val) rs368035421 0.00001
NC_000017.10:g.(?_647660)_(655505_?)dup
NM_015721.3(GEMIN4):c.1039C>T (p.Arg347Trp)
NM_015721.3(GEMIN4):c.1100G>A (p.Ser367Asn) rs758393066
NM_015721.3(GEMIN4):c.1216A>G (p.Ile406Val) rs763922214
NM_015721.3(GEMIN4):c.121C>G (p.Arg41Gly)
NM_015721.3(GEMIN4):c.1268A>G (p.Tyr423Cys)
NM_015721.3(GEMIN4):c.130C>G (p.Arg44Gly)
NM_015721.3(GEMIN4):c.1320C>G (p.Cys440Trp) rs2544542416
NM_015721.3(GEMIN4):c.1329T>A (p.Ser443Arg)
NM_015721.3(GEMIN4):c.1384A>G (p.Ile462Val) rs754798868
NM_015721.3(GEMIN4):c.1415C>T (p.Pro472Leu)
NM_015721.3(GEMIN4):c.1467C>G (p.Asp489Glu) rs764702336
NM_015721.3(GEMIN4):c.1487A>G (p.Asn496Ser)
NM_015721.3(GEMIN4):c.1545G>T (p.Leu515Phe)
NM_015721.3(GEMIN4):c.1573G>C (p.Asp525His)
NM_015721.3(GEMIN4):c.1651C>T (p.Arg551Cys)
NM_015721.3(GEMIN4):c.1670C>T (p.Pro557Leu)
NM_015721.3(GEMIN4):c.1721C>G (p.Thr574Ser)
NM_015721.3(GEMIN4):c.1771G>A (p.Val591Met) rs199702345
NM_015721.3(GEMIN4):c.1771G>C (p.Val591Leu)
NM_015721.3(GEMIN4):c.1795T>C (p.Ser599Pro) rs1446153691
NM_015721.3(GEMIN4):c.1802C>G (p.Thr601Ser) rs898791411
NM_015721.3(GEMIN4):c.1852C>T (p.Pro618Ser) rs1046242682
NM_015721.3(GEMIN4):c.1924G>T (p.Val642Leu)
NM_015721.3(GEMIN4):c.1940A>G (p.Glu647Gly)
NM_015721.3(GEMIN4):c.1964T>G (p.Phe655Cys) rs780061624
NM_015721.3(GEMIN4):c.1975T>G (p.Phe659Val)
NM_015721.3(GEMIN4):c.2194A>G (p.Ile732Val) rs2544537633
NM_015721.3(GEMIN4):c.2224G>A (p.Ala742Thr)
NM_015721.3(GEMIN4):c.227A>G (p.Lys76Arg)
NM_015721.3(GEMIN4):c.2281C>T (p.Arg761Cys)
NM_015721.3(GEMIN4):c.2282G>A (p.Arg761His)
NM_015721.3(GEMIN4):c.2282G>T (p.Arg761Leu)
NM_015721.3(GEMIN4):c.2293C>G (p.Gln765Glu)
NM_015721.3(GEMIN4):c.2419C>G (p.Pro807Ala)
NM_015721.3(GEMIN4):c.2426A>C (p.Tyr809Ser) rs2544536122
NM_015721.3(GEMIN4):c.2483T>A (p.Ile828Asn)
NM_015721.3(GEMIN4):c.2486C>T (p.Ser829Leu)
NM_015721.3(GEMIN4):c.2512G>A (p.Val838Met) rs1043083035
NM_015721.3(GEMIN4):c.2526T>G (p.Asn842Lys)
NM_015721.3(GEMIN4):c.2542C>A (p.Leu848Met)
NM_015721.3(GEMIN4):c.2557T>C (p.Phe853Leu)
NM_015721.3(GEMIN4):c.259G>A (p.Asp87Asn)
NM_015721.3(GEMIN4):c.2614C>G (p.Leu872Val) rs1427366129
NM_015721.3(GEMIN4):c.2649G>C (p.Gln883His) rs2544534617
NM_015721.3(GEMIN4):c.2702A>G (p.Asn901Ser) rs752849227
NM_015721.3(GEMIN4):c.2756T>C (p.Phe919Ser)
NM_015721.3(GEMIN4):c.2838T>G (p.Ser946Arg) rs2544533454
NM_015721.3(GEMIN4):c.2856C>G (p.Asp952Glu) rs1001070206
NM_015721.3(GEMIN4):c.3115G>C (p.Ala1039Pro)
NM_015721.3(GEMIN4):c.312C>G (p.Ile104Met) rs1904337692
NM_015721.3(GEMIN4):c.3142C>T (p.Arg1048Cys)
NM_015721.3(GEMIN4):c.3147A>T (p.Gln1049His)
NM_015721.3(GEMIN4):c.427C>T (p.Arg143Cys) rs1461565802
NM_015721.3(GEMIN4):c.484G>A (p.Asp162Asn)
NM_015721.3(GEMIN4):c.532C>G (p.Leu178Val) rs370503352
NM_015721.3(GEMIN4):c.547A>G (p.Ser183Gly) rs373751711
NM_015721.3(GEMIN4):c.557C>T (p.Ala186Val) rs2144173623
NM_015721.3(GEMIN4):c.661C>T (p.Arg221Cys) rs781259354
NM_015721.3(GEMIN4):c.662G>A (p.Arg221His)
NM_015721.3(GEMIN4):c.684T>G (p.Ser228Arg)
NM_015721.3(GEMIN4):c.698C>A (p.Pro233Gln)
NM_015721.3(GEMIN4):c.766G>C (p.Asp256His) rs531320666
NM_015721.3(GEMIN4):c.779T>G (p.Val260Gly)
NM_015721.3(GEMIN4):c.788C>T (p.Thr263Ile) rs371143590
NM_015721.3(GEMIN4):c.823G>C (p.Val275Leu)
NM_015721.3(GEMIN4):c.832T>G (p.Ser278Ala)
NM_015721.3(GEMIN4):c.855C>A (p.His285Gln)
NM_015721.3(GEMIN4):c.892C>T (p.Arg298Trp) rs201812530
NM_015721.3(GEMIN4):c.910T>G (p.Ser304Ala) rs1212951896
NM_015721.3(GEMIN4):c.920A>T (p.Lys307Ile)
NM_015721.3(GEMIN4):c.980G>T (p.Trp327Leu) rs200678582

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