ClinVar Miner

List of variants in gene DNAAF5 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_017802.4(DNAAF5):c.781G>A (p.Val261Ile) rs138915052 0.00063
NM_017802.4(DNAAF5):c.1208G>A (p.Arg403Gln) rs149778130 0.00039
NM_017802.4(DNAAF5):c.2510C>T (p.Ser837Leu) rs115620965 0.00021
NM_017802.4(DNAAF5):c.1499G>T (p.Cys500Phe) rs144405450 0.00010
NM_017802.4(DNAAF5):c.1246G>A (p.Val416Met) rs775542739 0.00006
NM_017802.4(DNAAF5):c.1375G>A (p.Ala459Thr) rs201942359 0.00005
NM_017802.4(DNAAF5):c.1487G>A (p.Arg496His) rs149610399 0.00005
NM_017802.4(DNAAF5):c.1715C>T (p.Ala572Val) rs147690117 0.00004
NM_017802.4(DNAAF5):c.1027C>T (p.Arg343Cys) rs773921234 0.00003
NM_017802.4(DNAAF5):c.1714G>A (p.Ala572Thr) rs534027051 0.00003
NM_017802.4(DNAAF5):c.1856C>T (p.Pro619Leu) rs755871359 0.00003
NM_017802.4(DNAAF5):c.802G>A (p.Val268Met) rs370267615 0.00003
NM_017802.4(DNAAF5):c.1586T>A (p.Leu529His) rs368098310 0.00001
NM_017802.4(DNAAF5):c.1997C>T (p.Ala666Val) rs761189541 0.00001

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