List of variants in gene TNPO3 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_012470.4(TNPO3):c.2661C>T (p.Ala887=)	rs8043	0.49045
NM_012470.4(TNPO3):c.759C>G (p.Leu253=)	rs2305324	0.35727
NM_012470.4(TNPO3):c.2062-12T>G	rs112438598	0.06913
NM_012470.4(TNPO3):c.2358G>A (p.Leu786=)	rs11538884	0.04242
NM_012470.4(TNPO3):c.2205C>T (p.Leu735=)	rs2293493	0.03941
NM_012470.4(TNPO3):c.321+16C>T	rs17424179	0.02517
NM_012470.4(TNPO3):c.2652C>T (p.Thr884=)	rs149434536	0.00140
NM_012470.4(TNPO3):c.2280T>C (p.Ile760=)	rs142359170	0.00093
NM_012470.4(TNPO3):c.2741C>T (p.Ala914Val)	rs61756249	0.00061
NM_012470.4(TNPO3):c.582T>C (p.Asp194=)	rs148885407	0.00041
NM_012470.4(TNPO3):c.275C>T (p.Thr92Ile)	rs61756250	0.00037
NM_012470.4(TNPO3):c.1416C>T (p.Thr472=)	rs368379579	0.00019
NM_012470.4(TNPO3):c.189T>C (p.Ala63=)	rs755216120	0.00001
NM_012470.4(TNPO3):c.873-3C>T	rs780935123	0.00001
NM_012470.4(TNPO3):c.1150C>T (p.Pro384Ser)
NM_012470.4(TNPO3):c.2082A>G (p.Val694=)
NM_012470.4(TNPO3):c.2179-8T>C
NM_012470.4(TNPO3):c.2583G>A (p.Met861Ile)

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