ClinVar Miner

List of variants in gene NDUFA9 reported by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_005002.5(NDUFA9):c.411-99G>A rs4766268 0.97742
NM_005002.5(NDUFA9):c.552+234G>A rs7957498 0.97737
NM_005002.5(NDUFA9):c.319-116T>C rs6489557 0.95225
NM_005002.5(NDUFA9):c.963+242A>G rs7978162 0.89229
NM_005002.5(NDUFA9):c.553-268A>G rs10849115 0.85364
NM_005002.5(NDUFA9):c.552+11A>C rs7972657 0.72251
NM_005002.5(NDUFA9):c.552+276A>G rs7972920 0.69174
NM_005002.5(NDUFA9):c.552+94C>T rs7958182 0.68923
NM_005002.5(NDUFA9):c.896+207A>G rs2302244 0.56154
NM_005002.5(NDUFA9):c.724-280A>G rs2240762 0.55777
NM_005002.5(NDUFA9):c.800+104A>G rs1009633 0.55612
NM_005002.5(NDUFA9):c.411-107T>C rs4147681 0.47803
NM_005002.5(NDUFA9):c.50-109C>T rs2302247 0.47397
NM_005002.5(NDUFA9):c.553-17G>A rs2267549 0.38648
NM_005002.5(NDUFA9):c.897-74A>G rs2240760 0.29556
NM_005002.5(NDUFA9):c.318+49G>A rs4147672 0.27653
NM_005002.5(NDUFA9):c.318+107C>T rs4147673 0.27273
NM_005002.5(NDUFA9):c.50-58G>C rs2302246 0.26859
NM_005002.5(NDUFA9):c.411-9A>T rs4147682 0.26203
NM_005002.5(NDUFA9):c.411-318A>T rs4147679 0.26062
NM_005002.5(NDUFA9):c.411-304A>G rs4147680 0.26059
NM_005002.5(NDUFA9):c.552+168A>G rs12318966 0.24990
NM_005002.5(NDUFA9):c.319-151C>T rs12309713 0.23352
NM_005002.5(NDUFA9):c.553-243G>A rs2267548 0.20395
NM_005002.5(NDUFA9):c.896+196C>A rs1029767 0.18326
NM_005002.5(NDUFA9):c.552+161C>T rs4147683 0.18031
NM_005002.5(NDUFA9):c.656-274C>T rs17701871 0.16992
NM_005002.5(NDUFA9):c.656-149G>A rs68144469 0.13238
NM_005002.5(NDUFA9):c.50-54G>C rs61909964 0.03607
NM_005002.5(NDUFA9):c.319-71G>A rs112635332 0.02025
NM_005002.5(NDUFA9):c.50-301A>G rs113630331 0.01784
NM_005002.5(NDUFA9):c.552+292C>G rs11834553 0.01775
NM_005002.5(NDUFA9):c.50-261G>C rs80097844 0.01258
NM_005002.5(NDUFA9):c.221-84A>G rs71579252 0.01004
NM_005002.5(NDUFA9):c.801-217G>A rs145392138 0.00998
NM_005002.5(NDUFA9):c.13G>C (p.Ala5Pro) rs35155742 0.00971
NM_005002.5(NDUFA9):c.*41G>A rs3210088 0.00962
NM_005002.5(NDUFA9):c.963+83C>T rs148955018 0.00895
NM_005002.5(NDUFA9):c.50-250A>G rs75606091 0.00381
NM_005002.5(NDUFA9):c.330G>T (p.Ala110=) rs148477287 0.00314
NM_005002.5(NDUFA9):c.942A>G (p.Ile314Met) rs139674448 0.00225
NM_005002.5(NDUFA9):c.655+17A>G rs149534005 0.00206
NM_005002.5(NDUFA9):c.1131T>G (p.Ile377Met) rs147407002 0.00198
NM_005002.5(NDUFA9):c.963+45C>T rs145777379 0.00072
NM_005002.5(NDUFA9):c.722A>G (p.Tyr241Cys) rs139012735 0.00068
NM_005002.5(NDUFA9):c.656-6C>T rs138785086 0.00058
NM_005002.5(NDUFA9):c.1104T>C (p.Asp368=) rs146190369 0.00047
NM_005002.5(NDUFA9):c.897-20A>G rs201371580 0.00036
NM_005002.5(NDUFA9):c.588G>A (p.Pro196=) rs138434279 0.00028
NM_005002.5(NDUFA9):c.253C>T (p.Arg85Trp) rs71579253 0.00026
NM_005002.5(NDUFA9):c.553-9A>G rs150765610 0.00021
NM_005002.5(NDUFA9):c.1062G>T (p.Arg354=) rs201530517 0.00016
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.656-5G>A rs184286793 0.00010
NM_005002.5(NDUFA9):c.1044G>A (p.Lys348=) rs774542402 0.00006
NM_005002.5(NDUFA9):c.655+5G>A rs768333416 0.00006
NM_005002.5(NDUFA9):c.31C>T (p.Arg11Trp) rs780895352 0.00005
NM_005002.5(NDUFA9):c.795C>T (p.Phe265=) rs1057521037 0.00005
NM_005002.5(NDUFA9):c.223C>T (p.Arg75Cys) rs767462328 0.00003
NM_005002.5(NDUFA9):c.27T>C (p.Val9=) rs1318411878 0.00003
NM_005002.5(NDUFA9):c.1123G>A (p.Val375Ile) rs768816594 0.00002
NM_005002.5(NDUFA9):c.666G>A (p.Arg222=) rs966066971 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.1005A>G (p.Leu335=) rs746459711 0.00001
NM_005002.5(NDUFA9):c.199C>T (p.Arg67Ter) rs758574474 0.00001
NM_005002.5(NDUFA9):c.219T>A (p.Leu73=) rs960949361 0.00001
NM_005002.5(NDUFA9):c.483T>A (p.Val161=) rs902398679 0.00001
NM_005002.5(NDUFA9):c.580G>A (p.Ala194Thr) rs863224085 0.00001
NM_005002.5(NDUFA9):c.1122C>T (p.Thr374=) rs139060466
NM_005002.5(NDUFA9):c.182C>T (p.Ala61Val) rs863224087
NM_005002.5(NDUFA9):c.220+156_220+157del rs3217056
NM_005002.5(NDUFA9):c.224G>T (p.Arg75Leu) rs35263902
NM_005002.5(NDUFA9):c.335A>G (p.Asp112Gly) rs2137464531
NM_005002.5(NDUFA9):c.552+180_552+181del rs34173659
NM_005002.5(NDUFA9):c.735A>G (p.Val245=) rs767410946
NM_005002.5(NDUFA9):c.796G>A (p.Val266Ile)
NM_005002.5(NDUFA9):c.800+145C>T rs78705685
NM_005002.5(NDUFA9):c.965T>C (p.Met322Thr) rs863224086

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