Variants in gene DNAAF1 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_178452.6(DNAAF1):c.1718T>C (p.Ile573Thr)	rs137862641	0.00237
NM_178452.6(DNAAF1):c.1664A>T (p.Asp555Val)	rs145973397	0.00178
NM_178452.6(DNAAF1):c.1567G>A (p.Val523Ile)	rs148387367	0.00167
NM_178452.6(DNAAF1):c.1354C>A (p.Pro452Thr)	rs145680314	0.00085
NM_178452.6(DNAAF1):c.546C>G (p.Asn182Lys)	rs144018942	0.00080
NM_178452.6(DNAAF1):c.1350G>A (p.Pro450=)	rs148990251	0.00026
NM_178452.6(DNAAF1):c.1083C>T (p.Gly361=)	rs200487337	0.00022
NM_178452.6(DNAAF1):c.115T>C (p.Cys39Arg)	rs373512514	0.00019
NM_178452.6(DNAAF1):c.2080G>A (p.Ala694Thr)	rs376164700	0.00007
NM_178452.6(DNAAF1):c.1592C>T (p.Thr531Met)	rs193291760	0.00005
NM_178452.6(DNAAF1):c.2083G>A (p.Ala695Thr)	rs775618173	0.00001
NM_178452.6(DNAAF1):c.13C>G (p.Pro5Ala)
NM_178452.6(DNAAF1):c.155G>A (p.Gly52Asp)
NM_178452.6(DNAAF1):c.1712C>T (p.Pro571Leu)	rs199727292
NM_178452.6(DNAAF1):c.1780G>A (p.Val594Met)
NM_178452.6(DNAAF1):c.2165C>T (p.Pro722Leu)
NM_178452.6(DNAAF1):c.491G>A (p.Arg164His)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.