List of variants in gene combination CCDC39, TTC14 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_181426.2(CCDC39):c.2397G>A (p.Val799=)	rs7612917	0.19015
NM_181426.2(CCDC39):c.2301G>A (p.Leu767=)	rs11914833	0.09489
NM_181426.2(CCDC39):c.2278A>G (p.Thr760Ala)	rs79386936	0.01017
NM_181426.2(CCDC39):c.2660dup (p.Ser888fs)	rs200353947	0.00844
NM_181426.2(CCDC39):c.2669+6C>T	rs57859179	0.00616
NM_181426.2(CCDC39):c.2432G>A (p.Arg811His)	rs61733583	0.00485
NM_181426.2(CCDC39):c.2299T>C (p.Leu767=)	rs200913298	0.00238
NM_181426.2(CCDC39):c.2534T>C (p.Ile845Thr)	rs139560004	0.00177
NM_181426.2(CCDC39):c.2409T>C (p.Cys803=)	rs201601768	0.00119
NM_181426.2(CCDC39):c.2266-5T>C	rs200409307	0.00017
NM_181426.2(CCDC39):c.2280A>G (p.Thr760=)	rs886038749	0.00001
NM_181426.2(CCDC39):c.2367G>A (p.Thr789=)	rs201806641	0.00001
NM_181426.2(CCDC39):c.2823A>G (p.Lys941=)	rs751844801	0.00001
NM_181426.2(CCDC39):c.2408G>A (p.Cys803Tyr)	rs561458801

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