ClinVar Miner

List of variants in gene DNAAF1 reported as likely benign for not specified

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_178452.6(DNAAF1):c.1227T>G (p.Gly409=) rs148674729 0.00342
NM_178452.6(DNAAF1):c.1718T>C (p.Ile573Thr) rs137862641 0.00237
NM_178452.6(DNAAF1):c.1245C>G (p.Thr415=) rs147804813 0.00233
NM_178452.6(DNAAF1):c.303G>C (p.Lys101Asn) rs140386513 0.00190
NM_178452.6(DNAAF1):c.1567G>A (p.Val523Ile) rs148387367 0.00167
NM_178452.6(DNAAF1):c.1031-5A>T rs79772571 0.00118
NM_178452.6(DNAAF1):c.432C>T (p.Ile144=) rs143312655 0.00063
NM_178452.6(DNAAF1):c.1988C>T (p.Pro663Leu) rs147393144 0.00053
NM_178452.6(DNAAF1):c.1299C>T (p.Asp433=) rs141074491 0.00044
NM_178452.6(DNAAF1):c.1350G>A (p.Pro450=) rs148990251 0.00026
NM_178452.6(DNAAF1):c.1030+14C>T rs202113269 0.00012
NM_178452.6(DNAAF1):c.507G>C (p.Leu169=) rs370128838 0.00011
NM_178452.6(DNAAF1):c.1317G>A (p.Glu439=) rs768024430 0.00009
NM_178452.6(DNAAF1):c.-19C>T rs369581422 0.00004
NM_178452.6(DNAAF1):c.1030+15G>A rs774316277 0.00004
NM_178452.6(DNAAF1):c.1197G>A (p.Pro399=) rs775507447
NM_178452.6(DNAAF1):c.1529-17TTG[2] rs369485504
NM_178452.6(DNAAF1):c.1989C>G (p.Pro663=) rs886038748
NM_178452.6(DNAAF1):c.2065+9G>C rs200690810
NM_178452.6(DNAAF1):c.864-17_864-14del rs141073777

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