ClinVar Miner

List of variants in gene NDUFA9 reported as uncertain significance for not provided

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Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_005002.5(NDUFA9):c.897-115A>G rs185994125 0.00193
NM_005002.5(NDUFA9):c.722A>G (p.Tyr241Cys) rs139012735 0.00068
NM_005002.5(NDUFA9):c.253C>T (p.Arg85Trp) rs71579253 0.00026
NM_005002.5(NDUFA9):c.665G>A (p.Arg222Gln) rs375511497 0.00023
NM_005002.5(NDUFA9):c.151G>A (p.Val51Ile) rs150945569 0.00017
NM_005002.5(NDUFA9):c.1012C>T (p.Leu338Phe) rs371795183 0.00013
NM_005002.5(NDUFA9):c.58A>G (p.Ile20Val) rs148447690 0.00012
NM_005002.5(NDUFA9):c.515C>T (p.Ala172Val) rs190837666 0.00009
NM_005002.5(NDUFA9):c.88G>A (p.Gly30Ser) rs529503724 0.00006
NM_005002.5(NDUFA9):c.31C>T (p.Arg11Trp) rs780895352 0.00005
NM_005002.5(NDUFA9):c.893A>G (p.Tyr298Cys) rs61754988 0.00005
NM_005002.5(NDUFA9):c.223C>T (p.Arg75Cys) rs767462328 0.00003
NM_005002.5(NDUFA9):c.823C>T (p.His275Tyr) rs377759212 0.00003
NM_005002.5(NDUFA9):c.1123G>A (p.Val375Ile) rs768816594 0.00002
NM_005002.5(NDUFA9):c.727G>A (p.Val243Ile) rs538700956 0.00002
NM_005002.5(NDUFA9):c.728T>C (p.Val243Ala) rs202214518 0.00002
NM_005002.5(NDUFA9):c.7G>A (p.Ala3Thr) rs201653293 0.00002
NM_005002.5(NDUFA9):c.1049T>C (p.Ile350Thr) rs772512870 0.00001
NM_005002.5(NDUFA9):c.142C>T (p.Arg48Cys) rs145275641 0.00001
NM_005002.5(NDUFA9):c.170C>T (p.Thr57Ile) rs1165725432 0.00001
NM_005002.5(NDUFA9):c.199C>T (p.Arg67Ter) rs758574474 0.00001
NM_005002.5(NDUFA9):c.205G>A (p.Val69Ile) rs368824479 0.00001
NM_005002.5(NDUFA9):c.328G>A (p.Ala110Thr) rs772426441 0.00001
NM_005002.5(NDUFA9):c.341A>T (p.Asp114Val) rs765033754 0.00001
NM_005002.5(NDUFA9):c.601G>T (p.Val201Leu) rs201865179 0.00001
NM_005002.5(NDUFA9):c.8C>T (p.Ala3Val) rs756216768 0.00001
NM_005002.5(NDUFA9):c.1006G>C (p.Glu336Gln) rs2137490326
NM_005002.5(NDUFA9):c.1018A>G (p.Ile340Val)
NM_005002.5(NDUFA9):c.1069C>T (p.Arg357Cys)
NM_005002.5(NDUFA9):c.1079G>A (p.Arg360His)
NM_005002.5(NDUFA9):c.1130T>C (p.Ile377Thr)
NM_005002.5(NDUFA9):c.1132T>A (p.Ter378Lys)
NM_005002.5(NDUFA9):c.122T>C (p.Met41Thr)
NM_005002.5(NDUFA9):c.128A>G (p.His43Arg) rs2137462111
NM_005002.5(NDUFA9):c.143G>A (p.Arg48His)
NM_005002.5(NDUFA9):c.182C>T (p.Ala61Val) rs863224087
NM_005002.5(NDUFA9):c.185C>T (p.Thr62Ile)
NM_005002.5(NDUFA9):c.19T>G (p.Ser7Ala)
NM_005002.5(NDUFA9):c.19delinsAC (p.Ser7fs)
NM_005002.5(NDUFA9):c.226A>G (p.Met76Val)
NM_005002.5(NDUFA9):c.241del (p.Ile81fs)
NM_005002.5(NDUFA9):c.266A>G (p.Tyr89Cys) rs1401024490
NM_005002.5(NDUFA9):c.283C>T (p.Arg95Cys)
NM_005002.5(NDUFA9):c.289A>G (p.Met97Val)
NM_005002.5(NDUFA9):c.302G>A (p.Gly101Asp) rs1394888431
NM_005002.5(NDUFA9):c.318+6G>A rs766530587
NM_005002.5(NDUFA9):c.335A>G (p.Asp112Gly) rs2137464531
NM_005002.5(NDUFA9):c.349C>T (p.Arg117Ter)
NM_005002.5(NDUFA9):c.365A>C (p.His122Pro)
NM_005002.5(NDUFA9):c.372T>G (p.Asn124Lys)
NM_005002.5(NDUFA9):c.383A>G (p.Asn128Ser)
NM_005002.5(NDUFA9):c.395G>A (p.Arg132Gln)
NM_005002.5(NDUFA9):c.397G>C (p.Asp133His)
NM_005002.5(NDUFA9):c.470A>G (p.Lys157Arg)
NM_005002.5(NDUFA9):c.49+6T>C rs2137457763
NM_005002.5(NDUFA9):c.50-7_50-4del
NM_005002.5(NDUFA9):c.552+5G>A
NM_005002.5(NDUFA9):c.587C>T (p.Pro196Leu)
NM_005002.5(NDUFA9):c.608C>T (p.Pro203Leu)
NM_005002.5(NDUFA9):c.611C>T (p.Ser204Leu)
NM_005002.5(NDUFA9):c.616A>G (p.Ile206Val)
NM_005002.5(NDUFA9):c.621T>A (p.Phe207Leu)
NM_005002.5(NDUFA9):c.634A>G (p.Arg212Gly)
NM_005002.5(NDUFA9):c.655+4C>T
NM_005002.5(NDUFA9):c.660G>A (p.Met220Ile)
NM_005002.5(NDUFA9):c.661C>T (p.His221Tyr)
NM_005002.5(NDUFA9):c.664C>G (p.Arg222Gly)
NM_005002.5(NDUFA9):c.677T>C (p.Ile226Thr) rs758519893
NM_005002.5(NDUFA9):c.68T>C (p.Ile23Thr)
NM_005002.5(NDUFA9):c.694G>C (p.Gly232Arg)
NM_005002.5(NDUFA9):c.770A>G (p.Asp257Gly)
NM_005002.5(NDUFA9):c.796G>A (p.Val266Ile)
NM_005002.5(NDUFA9):c.799G>A (p.Gly267Ser)
NM_005002.5(NDUFA9):c.806G>C (p.Ser269Thr)
NM_005002.5(NDUFA9):c.808C>A (p.Arg270=)
NM_005002.5(NDUFA9):c.808C>T (p.Arg270Trp)
NM_005002.5(NDUFA9):c.824A>T (p.His275Leu)
NM_005002.5(NDUFA9):c.850G>A (p.Ala284Thr)
NM_005002.5(NDUFA9):c.872T>G (p.Phe291Cys)
NM_005002.5(NDUFA9):c.892T>C (p.Tyr298His)
NM_005002.5(NDUFA9):c.896G>A (p.Arg299Gln)
NM_005002.5(NDUFA9):c.92C>T (p.Pro31Leu)
NM_005002.5(NDUFA9):c.94C>A (p.Pro32Thr)
NM_005002.5(NDUFA9):c.962G>A (p.Arg321Gln)
NM_005002.5(NDUFA9):c.963+5G>C
NM_005002.5(NDUFA9):c.965T>C (p.Met322Thr) rs863224086
NM_005002.5(NDUFA9):c.989C>G (p.Pro330Arg)

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