List of variants in gene COQ9 reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 112

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HGVS	dbSNP	gnomAD frequency
NM_020312.4(COQ9):c.607-162C>T	rs223867	0.02806
NM_020312.4(COQ9):c.712-194G>A	rs118076482	0.02471
NM_020312.4(COQ9):c.379-273G>C	rs77838762	0.02050
NM_020312.4(COQ9):c.242+250C>A	rs8044899	0.01552
NM_020312.4(COQ9):c.712-180A>C	rs11867042	0.01174
NM_020312.4(COQ9):c.243-287C>T	rs112828335	0.00865
NM_020312.4(COQ9):c.712-215_712-211del	rs145473540	0.00586
NM_020312.4(COQ9):c.242+73T>A	rs143751432	0.00376
NM_020312.4(COQ9):c.835G>A (p.Asp279Asn)	rs76508383	0.00282
NM_020312.4(COQ9):c.826C>T (p.Arg276Trp)	rs143587648	0.00272
NM_020312.4(COQ9):c.625C>G (p.Leu209Val)	rs78846023	0.00217
NM_020312.4(COQ9):c.323T>G (p.Leu108Arg)	rs11547480	0.00101
NM_020312.4(COQ9):c.467G>A (p.Arg156Gln)	rs201097286	0.00027
NM_020312.4(COQ9):c.513C>T (p.Gly171=)	rs144219851	0.00016
NM_020312.4(COQ9):c.607-16G>A	rs74019520	0.00016
NM_020312.4(COQ9):c.357G>A (p.Glu119=)	rs202128398	0.00011
NM_020312.4(COQ9):c.741G>A (p.Leu247=)	rs144686029	0.00007
NM_020312.4(COQ9):c.642G>A (p.Pro214=)	rs374294033	0.00006
NM_020312.4(COQ9):c.261C>T (p.Gly87=)	rs376613524	0.00005
NM_020312.4(COQ9):c.315G>A (p.Thr105=)	rs201238241	0.00004
NM_020312.4(COQ9):c.691G>T (p.Ala231Ser)	rs368375933	0.00003
NM_020312.4(COQ9):c.711+14G>A	rs371431812	0.00003
NM_020312.4(COQ9):c.362T>C (p.Ile121Thr)	rs547254482	0.00002
NM_020312.4(COQ9):c.162T>G (p.Pro54=)	rs757869710	0.00001
NM_020312.4(COQ9):c.336C>T (p.Pro112=)	rs779510052	0.00001
NM_020312.4(COQ9):c.337G>A (p.Ala113Thr)	rs377307935	0.00001
NM_020312.4(COQ9):c.342C>T (p.His114=)	rs771763396	0.00001
NM_020312.4(COQ9):c.378+9A>G	rs757816546	0.00001
NM_020312.4(COQ9):c.379-20T>C	rs776191682	0.00001
NM_020312.4(COQ9):c.379-9C>T	rs1189201208	0.00001
NM_020312.4(COQ9):c.414C>T (p.Phe138=)	rs780413033	0.00001
NM_020312.4(COQ9):c.492G>A (p.Glu164=)	rs200465461	0.00001
NM_020312.4(COQ9):c.783C>T (p.Asp261=)	rs1248544273	0.00001
NM_020312.4(COQ9):c.867+10G>A	rs746182554	0.00001
NM_020312.4(COQ9):c.868-12G>A	rs763229856	0.00001
NM_020312.4(COQ9):c.120A>C (p.Ser40=)
NM_020312.4(COQ9):c.132A>G (p.Leu44=)
NM_020312.4(COQ9):c.147G>A (p.Glu49=)
NM_020312.4(COQ9):c.204A>T (p.Ala68=)
NM_020312.4(COQ9):c.242+16C>T
NM_020312.4(COQ9):c.243-11T>A
NM_020312.4(COQ9):c.243-12C>G
NM_020312.4(COQ9):c.243-255G>T	rs192310711
NM_020312.4(COQ9):c.267G>A (p.Glu89=)
NM_020312.4(COQ9):c.273G>A (p.Glu91=)	rs1301403024
NM_020312.4(COQ9):c.276C>T (p.Asp92=)
NM_020312.4(COQ9):c.285T>C (p.Ser95=)
NM_020312.4(COQ9):c.318A>C (p.Ala106=)
NM_020312.4(COQ9):c.360G>A (p.Ala120=)
NM_020312.4(COQ9):c.378+10G>C	rs1598037166
NM_020312.4(COQ9):c.378+8T>C
NM_020312.4(COQ9):c.379-11C>T
NM_020312.4(COQ9):c.379-12C>A
NM_020312.4(COQ9):c.379-14C>T
NM_020312.4(COQ9):c.379-16G>A	rs62037144
NM_020312.4(COQ9):c.387T>G (p.Gly129=)
NM_020312.4(COQ9):c.408C>T (p.Ser136=)
NM_020312.4(COQ9):c.423T>C (p.Asp141=)
NM_020312.4(COQ9):c.429T>C (p.Ser143=)
NM_020312.4(COQ9):c.444T>C (p.His148=)
NM_020312.4(COQ9):c.453C>G (p.Thr151=)	rs2146590868
NM_020312.4(COQ9):c.456G>A (p.Gln152=)
NM_020312.4(COQ9):c.462T>C (p.Asn154=)
NM_020312.4(COQ9):c.465C>G (p.Thr155=)
NM_020312.4(COQ9):c.468G>A (p.Arg156=)
NM_020312.4(COQ9):c.519G>A (p.Ala173=)
NM_020312.4(COQ9):c.521+15A>G
NM_020312.4(COQ9):c.521+18A>G
NM_020312.4(COQ9):c.522-10C>T
NM_020312.4(COQ9):c.522-11C>T
NM_020312.4(COQ9):c.522-7C>T
NM_020312.4(COQ9):c.522-9C>A
NM_020312.4(COQ9):c.549G>A (p.Arg183=)
NM_020312.4(COQ9):c.606+10C>G
NM_020312.4(COQ9):c.618C>T (p.Ile206=)
NM_020312.4(COQ9):c.627C>G (p.Leu209=)
NM_020312.4(COQ9):c.649C>T (p.Leu217=)
NM_020312.4(COQ9):c.651G>A (p.Leu217=)
NM_020312.4(COQ9):c.655C>T (p.Leu219=)
NM_020312.4(COQ9):c.708T>C (p.Thr236=)
NM_020312.4(COQ9):c.712-16G>C
NM_020312.4(COQ9):c.712-17T>C
NM_020312.4(COQ9):c.714T>C (p.Phe238=)
NM_020312.4(COQ9):c.723C>T (p.Tyr241=)
NM_020312.4(COQ9):c.729C>G (p.Arg243=)
NM_020312.4(COQ9):c.73+17G>A
NM_020312.4(COQ9):c.73+20G>T
NM_020312.4(COQ9):c.74-10del
NM_020312.4(COQ9):c.74-20C>T
NM_020312.4(COQ9):c.741G>C (p.Leu247=)
NM_020312.4(COQ9):c.744T>C (p.Ala248=)
NM_020312.4(COQ9):c.798T>C (p.Phe266=)
NM_020312.4(COQ9):c.79C>G (p.Arg27Gly)	rs140264612
NM_020312.4(COQ9):c.831T>C (p.Val277=)
NM_020312.4(COQ9):c.831T>G (p.Val277=)
NM_020312.4(COQ9):c.858T>C (p.Thr286=)
NM_020312.4(COQ9):c.867+18A>G
NM_020312.4(COQ9):c.867+7G>A
NM_020312.4(COQ9):c.868-20C>T
NM_020312.4(COQ9):c.870A>G (p.Val290=)
NM_020312.4(COQ9):c.894G>A (p.Val298=)
NM_020312.4(COQ9):c.921+12C>T
NM_020312.4(COQ9):c.921+14A>T
NM_020312.4(COQ9):c.921+17A>T
NM_020312.4(COQ9):c.922-10C>T	rs1288687526
NM_020312.4(COQ9):c.922-14C>T
NM_020312.4(COQ9):c.922-7G>A
NM_020312.4(COQ9):c.922-7G>T
NM_020312.4(COQ9):c.922-8C>T
NM_020312.4(COQ9):c.924C>G (p.Leu308=)
NM_020312.4(COQ9):c.924C>T (p.Leu308=)
NM_020312.4(COQ9):c.96G>T (p.Leu32=)

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