List of variants in gene TNPO3 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: 50

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HGVS	dbSNP	gnomAD frequency
NM_012470.4(TNPO3):c.1859+242C>G	rs73463042	0.02314
NM_012470.4(TNPO3):c.2599-78G>A	rs73463020	0.02308
NM_012470.4(TNPO3):c.2061+179C>T	rs144953867	0.01361
NM_012470.4(TNPO3):c.1012-271A>G	rs28607116	0.01359
NM_012470.4(TNPO3):c.120+184C>G	rs10266077	0.01201
NM_012470.4(TNPO3):c.1921-205A>G	rs141992296	0.01153
NM_012470.4(TNPO3):c.553-116T>C	rs1495462	0.01096
NM_012470.4(TNPO3):c.2430+154A>G	rs10276681	0.01039
NM_012470.4(TNPO3):c.1012-326C>T	rs144370208	0.00786
NM_012470.4(TNPO3):c.697-249C>T	rs111226894	0.00775
NM_012470.4(TNPO3):c.395+29G>A	rs138284925	0.00754
NM_012470.4(TNPO3):c.1011+148T>A	rs182945121	0.00749
NM_012470.4(TNPO3):c.2599-268C>T	rs144859720	0.00710
NM_012470.4(TNPO3):c.2711+287G>A	rs115663147	0.00709
NM_012470.4(TNPO3):c.2712-267A>G	rs115442046	0.00594
NM_012470.4(TNPO3):c.2061+188G>A	rs141449280	0.00580
NM_012470.4(TNPO3):c.1011+56T>C	rs7807327	0.00541
NM_012470.4(TNPO3):c.321+31T>C	rs116830152	0.00540
NM_012470.4(TNPO3):c.2598+245A>G	rs143326920	0.00531
NC_000007.14:g.129055497T>C	rs114666055	0.00493
NM_012470.4(TNPO3):c.2273+133A>G	rs1874331	0.00483
NM_012470.4(TNPO3):c.1011+322A>C	rs79089815	0.00441
NM_012470.4(TNPO3):c.2062-34G>A	rs75544053	0.00440
NM_012470.4(TNPO3):c.2061+75T>C	rs138805125	0.00423
NM_012470.4(TNPO3):c.121-30T>G	rs147557723	0.00384
NM_012470.4(TNPO3):c.321+27A>G	rs149868719	0.00341
NM_012470.4(TNPO3):c.2178+26C>T	rs148454273	0.00340
NM_012470.4(TNPO3):c.2061+26G>A	rs185942627	0.00067
NM_012470.4(TNPO3):c.120+9C>A	rs372906002	0.00048
NM_012470.4(TNPO3):c.275C>T (p.Thr92Ile)	rs61756250	0.00034
NM_012470.4(TNPO3):c.2061+18G>A	rs376309645	0.00026
NM_012470.4(TNPO3):c.2274-5A>G	rs567711266	0.00005
NM_012470.4(TNPO3):c.2431-6A>C	rs190759031	0.00005
NM_012470.4(TNPO3):c.738G>A (p.Ser246=)	rs779514660	0.00004
NM_012470.4(TNPO3):c.1011+20A>G	rs199605219	0.00003
NM_012470.4(TNPO3):c.1158+17A>G	rs764995047	0.00003
NM_012470.4(TNPO3):c.2385C>T (p.Val795=)	rs1057064473	0.00002
NM_012470.4(TNPO3):c.1209A>G (p.Val403=)	rs754874514	0.00001
NM_012470.4(TNPO3):c.1810A>G (p.Ile604Val)	rs886043402	0.00001
NM_012470.4(TNPO3):c.1899G>A (p.Pro633=)	rs747905488	0.00001
NM_012470.4(TNPO3):c.2061+17C>T	rs190490751	0.00001
NM_012470.4(TNPO3):c.2256G>T (p.Leu752=)	rs1351482070	0.00001
NM_012470.4(TNPO3):c.322-16A>G	rs768458902	0.00001
NM_012470.4(TNPO3):c.873-3C>T	rs780935123	0.00001
NM_012470.4(TNPO3):c.148T>C (p.Leu50=)	rs1057523314
NM_012470.4(TNPO3):c.1783-303AAT[3]	rs199516284
NM_012470.4(TNPO3):c.2061+17C>A	rs190490751
NM_012470.4(TNPO3):c.2061+18dup	rs145442081
NM_012470.4(TNPO3):c.2406C>G (p.Leu802=)	rs1554435539
NM_012470.4(TNPO3):c.2430+199dup	rs566362874

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