List of variants in gene NDUFA10 reported as likely benign by GeneDx

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: 42

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HGVS	dbSNP	gnomAD frequency
NM_004544.4(NDUFA10):c.891-155_891-152del	rs140247225	0.02132
NM_004544.4(NDUFA10):c.*396C>G	rs73103629	0.01256
NM_004544.4(NDUFA10):c.670-274A>G	rs141638276	0.01144
NM_004544.4(NDUFA10):c.*2133A>G	rs6736791	0.01130
NM_004544.4(NDUFA10):c.*1878C>T	rs80067639	0.01081
NM_004544.4(NDUFA10):c.804+122T>C	rs114466901	0.00955
NM_004544.4(NDUFA10):c.75+131C>T	rs113286124	0.00907
NM_004544.4(NDUFA10):c.*647C>T	rs116254382	0.00794
NM_004544.4(NDUFA10):c.669+172C>T	rs115959597	0.00528
NC_000002.12:g.240025515G>A	rs186003789	0.00514
NM_004544.4(NDUFA10):c.76-277A>G	rs142328229	0.00367
NM_004544.4(NDUFA10):c.750-86G>A	rs116675569	0.00353
NM_004544.4(NDUFA10):c.999+67C>T	rs549261468	0.00189
NM_004544.4(NDUFA10):c.461-3C>T	rs199699869	0.00128
NM_004544.4(NDUFA10):c.749+16G>A	rs375221991	0.00095
NM_004544.4(NDUFA10):c.890+46G>C	rs61035353	0.00084
NM_004544.4(NDUFA10):c.1000-5C>G	rs201255198	0.00048
NM_004544.4(NDUFA10):c.804+48T>C	rs193112340	0.00027
NM_004544.4(NDUFA10):c.749+11C>T	rs200760509	0.00019
NM_004544.4(NDUFA10):c.312C>T (p.Leu104=)	rs145407882	0.00014
NM_004544.4(NDUFA10):c.548-15T>C	rs367815275	0.00013
NM_004544.4(NDUFA10):c.-37C>G	rs532866878	0.00010
NM_004544.4(NDUFA10):c.749+15C>T	rs369729748	0.00009
NM_004544.4(NDUFA10):c.1005G>A (p.Pro335=)	rs778173280	0.00006
NM_004544.4(NDUFA10):c.461-12A>G	rs372439113	0.00006
NM_004544.4(NDUFA10):c.71G>T (p.Arg24Leu)	rs863224083	0.00006
NM_004544.4(NDUFA10):c.76-9G>A	rs751528462	0.00006
NM_004544.4(NDUFA10):c.354C>T (p.Tyr118=)	rs118106981	0.00005
NM_004544.4(NDUFA10):c.549T>C (p.Cys183=)	rs149783296	0.00004
NM_004544.4(NDUFA10):c.*3G>A	rs758335453	0.00003
NM_004544.4(NDUFA10):c.297A>G (p.Gly99=)	rs1057523358	0.00003
NM_004544.4(NDUFA10):c.805-9C>T	rs775294758	0.00003
NM_004544.4(NDUFA10):c.264A>G (p.Glu88=)	rs776242214	0.00001
NM_004544.4(NDUFA10):c.516G>A (p.Ala172=)	rs762553028	0.00001
NM_004544.4(NDUFA10):c.547+18A>G	rs748355238	0.00001
NM_004544.4(NDUFA10):c.870T>C (p.Thr290=)	rs765127812	0.00001
NM_004544.4(NDUFA10):c.*8G>T	rs370647399
NM_004544.4(NDUFA10):c.1032C>T (p.Asn344=)	rs1019794328
NM_004544.4(NDUFA10):c.215A>G (p.Lys72Arg)	rs863224080
NM_004544.4(NDUFA10):c.669+65del	rs34961080
NM_004544.4(NDUFA10):c.804+12G>C	rs1318677453
NM_004544.4(NDUFA10):c.891-215C>A	rs111871664

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