ClinVar Miner

List of variants in gene INO80D reported as uncertain significance for not specified

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Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_017759.5(INO80D):c.833C>G (p.Pro278Arg) rs200938296 0.00094
NM_017759.5(INO80D):c.383G>C (p.Gly128Ala) rs202127822 0.00038
NM_017759.5(INO80D):c.1196G>A (p.Arg399Gln) rs200519220 0.00035
NM_017759.5(INO80D):c.2348A>G (p.Gln783Arg) rs374462979 0.00015
NM_017759.5(INO80D):c.1666C>T (p.Arg556Cys) rs368082888 0.00011
NM_017759.5(INO80D):c.1351G>A (p.Val451Met) rs754767138 0.00007
NM_017759.5(INO80D):c.764C>T (p.Ala255Val) rs533369239 0.00006
NM_017759.5(INO80D):c.2501A>G (p.His834Arg) rs542653405 0.00005
NM_017759.5(INO80D):c.3053A>G (p.Asn1018Ser) rs759356199 0.00005
NM_017759.5(INO80D):c.1571G>A (p.Arg524His) rs769913280 0.00004
NM_017759.5(INO80D):c.668C>T (p.Ala223Val) rs371646344 0.00003
NM_017759.5(INO80D):c.920G>A (p.Cys307Tyr) rs200755221 0.00003
NM_017759.5(INO80D):c.1012C>G (p.Gln338Glu) rs376594097 0.00002
NM_017759.5(INO80D):c.769C>G (p.Gln257Glu) rs774994130 0.00002
NM_017759.5(INO80D):c.1007C>T (p.Ser336Leu) rs755751160 0.00001
NM_017759.5(INO80D):c.1024T>C (p.Tyr342His) rs767743342 0.00001
NM_017759.5(INO80D):c.1046G>A (p.Arg349Gln) rs376007552 0.00001
NM_017759.5(INO80D):c.1246T>A (p.Cys416Ser) rs1163915802 0.00001
NM_017759.5(INO80D):c.1348A>T (p.Thr450Ser) rs369566340 0.00001
NM_017759.5(INO80D):c.1759C>T (p.Arg587Trp) rs557304541 0.00001
NM_017759.5(INO80D):c.2012T>C (p.Ile671Thr) rs748552208 0.00001
NM_017759.5(INO80D):c.2032G>C (p.Asp678His) rs779232035 0.00001
NM_017759.5(INO80D):c.2066G>A (p.Gly689Glu) rs768886465 0.00001
NM_017759.5(INO80D):c.20T>C (p.Ile7Thr) rs745458624 0.00001
NM_017759.5(INO80D):c.2120G>A (p.Arg707Gln) rs775445232 0.00001
NM_017759.5(INO80D):c.2237C>T (p.Thr746Ile) rs781503649 0.00001
NM_017759.5(INO80D):c.2696A>G (p.Asp899Gly) rs1315597888 0.00001
NM_017759.5(INO80D):c.2768C>T (p.Thr923Ile) rs761951615 0.00001
NM_017759.5(INO80D):c.298G>A (p.Val100Met) rs778667830 0.00001
NM_017759.5(INO80D):c.985A>G (p.Ser329Gly) rs1189105383 0.00001
NM_017759.5(INO80D):c.1052C>A (p.Thr351Asn) rs1689199329
NM_017759.5(INO80D):c.1097G>A (p.Ser366Asn) rs2469703567
NM_017759.5(INO80D):c.1239A>T (p.Glu413Asp)
NM_017759.5(INO80D):c.1257G>T (p.Gln419His)
NM_017759.5(INO80D):c.1300A>G (p.Ile434Val) rs770510485
NM_017759.5(INO80D):c.1306C>G (p.Arg436Gly)
NM_017759.5(INO80D):c.1342A>G (p.Ser448Gly)
NM_017759.5(INO80D):c.145A>G (p.Lys49Glu) rs1689722743
NM_017759.5(INO80D):c.1657C>T (p.Arg553Cys)
NM_017759.5(INO80D):c.1729G>A (p.Val577Ile)
NM_017759.5(INO80D):c.1950A>C (p.Glu650Asp)
NM_017759.5(INO80D):c.2074G>T (p.Val692Leu)
NM_017759.5(INO80D):c.2159G>A (p.Arg720His)
NM_017759.5(INO80D):c.219G>C (p.Arg73Ser) rs1409578530
NM_017759.5(INO80D):c.2261G>T (p.Gly754Val) rs2469601769
NM_017759.5(INO80D):c.227A>G (p.Asn76Ser)
NM_017759.5(INO80D):c.2339T>C (p.Phe780Ser) rs2469601149
NM_017759.5(INO80D):c.2486A>G (p.His829Arg)
NM_017759.5(INO80D):c.2641G>A (p.Gly881Arg) rs1687979621
NM_017759.5(INO80D):c.2647G>A (p.Val883Met)
NM_017759.5(INO80D):c.2725G>A (p.Ala909Thr)
NM_017759.5(INO80D):c.2774C>T (p.Ser925Leu)
NM_017759.5(INO80D):c.2803G>A (p.Ala935Thr) rs202107782
NM_017759.5(INO80D):c.2809G>A (p.Val937Met) rs777518928
NM_017759.5(INO80D):c.2845C>T (p.Pro949Ser)
NM_017759.5(INO80D):c.2852C>G (p.Thr951Ser) rs1410696557
NM_017759.5(INO80D):c.2900C>T (p.Ser967Phe)
NM_017759.5(INO80D):c.326T>C (p.Met109Thr)
NM_017759.5(INO80D):c.397C>T (p.Pro133Ser)
NM_017759.5(INO80D):c.421C>T (p.His141Tyr) rs2469818581
NM_017759.5(INO80D):c.487G>C (p.Gly163Arg)
NM_017759.5(INO80D):c.493A>G (p.Thr165Ala)
NM_017759.5(INO80D):c.644T>C (p.Leu215Ser)
NM_017759.5(INO80D):c.649A>G (p.Thr217Ala)
NM_017759.5(INO80D):c.653C>A (p.Ser218Tyr)
NM_017759.5(INO80D):c.653C>T (p.Ser218Phe)
NM_017759.5(INO80D):c.664C>A (p.Pro222Thr)
NM_017759.5(INO80D):c.668C>G (p.Ala223Gly)
NM_017759.5(INO80D):c.671C>T (p.Pro224Leu)
NM_017759.5(INO80D):c.674C>T (p.Pro225Leu)
NM_017759.5(INO80D):c.707A>C (p.Gln236Pro)
NM_017759.5(INO80D):c.778C>A (p.His260Asn)
NM_017759.5(INO80D):c.854T>C (p.Met285Thr)
NM_017759.5(INO80D):c.882C>G (p.Phe294Leu) rs2469815028
NM_017759.5(INO80D):c.944C>T (p.Thr315Ile)
NM_017759.5(INO80D):c.997C>T (p.Pro333Ser)

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