List of variants in gene OPA3 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: 37

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HGVS	dbSNP	gnomAD frequency
NM_025136.4(OPA3):c.*7015G>A	rs112948303	0.04300
NM_025136.4(OPA3):c.*6394G>A	rs151030695	0.02197
NM_025136.4(OPA3):c.143-174C>T	rs34508139	0.01902
NM_025136.4(OPA3):c.*7085A>G	rs67373144	0.01608
NM_025136.4(OPA3):c.*6275T>C	rs74689727	0.01461
NM_025136.4(OPA3):c.*1760C>T	rs75401979	0.01143
NM_025136.4(OPA3):c.*4794C>T	rs114917731	0.01114
NM_025136.4(OPA3):c.*1836C>T	rs74717111	0.01070
NM_025136.4(OPA3):c.*3222C>T	rs73568980	0.00971
NM_025136.4(OPA3):c.*6294A>C	rs114655581	0.00810
NM_025136.4(OPA3):c.*1855T>C	rs146599259	0.00697
NM_025136.4(OPA3):c.*5905G>A	rs116705343	0.00675
NM_025136.4(OPA3):c.142+81T>C	rs113539314	0.00669
NM_025136.4(OPA3):c.*362T>C	rs73942919	0.00539
NM_025136.4(OPA3):c.*5365C>T	rs73568970	0.00529
NM_025136.4(OPA3):c.*6442A>G	rs76825983	0.00518
NM_025136.4(OPA3):c.*1642A>G	rs144894771	0.00484
NM_025136.4(OPA3):c.*4954C>T	rs146646433	0.00462
NM_025136.4(OPA3):c.*6208C>T	rs139798464	0.00458
NC_000019.10:g.45584961T>C	rs115153567	0.00441
NM_025136.4(OPA3):c.*6101A>G	rs187296782	0.00363
NM_025136.4(OPA3):c.537A>G (p.Lys179=)	rs140105522	0.00158
NM_025136.4(OPA3):c.249G>C (p.Leu83=)	rs199692583	0.00080
NM_025136.4(OPA3):c.143-7C>T	rs375551151	0.00036
NM_001017989.3(OPA3):c.486C>T (p.His162=)	rs201078416	0.00022
NM_001017989.3(OPA3):c.*2A>T	rs190812374	0.00009
NM_025136.4(OPA3):c.336G>A (p.Glu112=)	rs146349367	0.00002
NM_025136.4(OPA3):c.519A>G (p.Ala173=)	rs1200579847	0.00002
NM_025136.4(OPA3):c.508G>A (p.Ala170Thr)	rs374639297	0.00001
NM_001017989.3(OPA3):c.222T>G (p.Gly74=)	rs1057520935
NM_025136.4(OPA3):c.4857_4858insC
NM_025136.4(OPA3):c.6104_6105del	rs142661638
NM_025136.4(OPA3):c.*6289A>G	rs182293743
NM_025136.4(OPA3):c.216C>T (p.Asn72=)	rs772750356
NM_025136.4(OPA3):c.273C>T (p.Ile91=)	rs369545089
NM_025136.4(OPA3):c.445C>T (p.Leu149=)	rs1057523113
NM_025136.4(OPA3):c.532A>G (p.Lys178Glu)	rs767372876

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