ClinVar Miner

List of variants in gene DNAAF1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 28
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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.303G>C (p.Lys101Asn) rs140386513 0.00190
NM_178452.6(DNAAF1):c.1664A>T (p.Asp555Val) rs145973397 0.00178
NM_178452.6(DNAAF1):c.1031-5A>T rs79772571 0.00118
NM_178452.6(DNAAF1):c.113G>C (p.Gly38Ala) rs200992452 0.00086
NM_178452.6(DNAAF1):c.1354C>A (p.Pro452Thr) rs145680314 0.00085
NM_178452.6(DNAAF1):c.432C>T (p.Ile144=) rs143312655 0.00063
NM_178452.6(DNAAF1):c.1495C>A (p.Pro499Thr) rs201519478 0.00050
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.361C>T (p.Arg121Cys) rs368031148 0.00013
NM_178452.6(DNAAF1):c.1030+14C>T rs202113269 0.00012
NM_178452.6(DNAAF1):c.2065+5G>A rs774606576 0.00011
NM_178452.6(DNAAF1):c.2079C>T (p.Ser693=) rs145469545 0.00011
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.1735T>C (p.Leu579=) rs764511452 0.00009
NM_178452.6(DNAAF1):c.141G>C (p.Lys47Asn) rs186287554 0.00006
NM_178452.6(DNAAF1):c.768G>A (p.Pro256=) rs142601761 0.00006
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.315C>G (p.Thr105=) rs144962513 0.00003
NM_178452.6(DNAAF1):c.1197G>A (p.Pro399=) rs775507447
NM_178452.6(DNAAF1):c.1529-17TTG[2] rs369485504
NM_178452.6(DNAAF1):c.1699-3T>C
NM_178452.6(DNAAF1):c.1989C>G (p.Pro663=) rs886038748
NM_178452.6(DNAAF1):c.2065+9G>C rs200690810

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