ClinVar Miner

List of variants in gene ZFYVE26 reported as uncertain significance by Athena Diagnostics Inc

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Gene type:
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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_015346.4(ZFYVE26):c.5260G>A (p.Ala1754Thr) rs146968463 0.00045
NM_015346.4(ZFYVE26):c.6448C>T (p.Pro2150Ser) rs138423670 0.00042
NM_015346.4(ZFYVE26):c.2300G>A (p.Arg767His) rs146290086 0.00037
NM_015346.4(ZFYVE26):c.3950C>T (p.Thr1317Met) rs143719747 0.00031
NM_015346.4(ZFYVE26):c.6154G>A (p.Val2052Ile) rs201273304 0.00018
NM_015346.4(ZFYVE26):c.1482C>A (p.Asn494Lys) rs559473389 0.00014
NM_015346.4(ZFYVE26):c.3802C>T (p.Leu1268Phe) rs202021708 0.00014
NM_015346.4(ZFYVE26):c.7128+4C>T rs374198908 0.00010
NM_015346.4(ZFYVE26):c.2010C>G (p.His670Gln) rs749925808 0.00005
NM_015346.4(ZFYVE26):c.6560G>A (p.Arg2187Gln) rs151306544 0.00004
NM_015346.4(ZFYVE26):c.361G>A (p.Glu121Lys) rs201229339 0.00003
NM_015346.4(ZFYVE26):c.1462C>T (p.His488Tyr) rs145455748 0.00002
NM_015346.4(ZFYVE26):c.2773A>G (p.Ile925Val) rs776812324 0.00001
NM_015346.4(ZFYVE26):c.5003G>A (p.Arg1668Gln) rs1239889656 0.00001
NM_015346.4(ZFYVE26):c.1958C>T (p.Pro653Leu) rs1566893050
NM_015346.4(ZFYVE26):c.2021G>A (p.Gly674Asp)
NM_015346.4(ZFYVE26):c.2173C>T (p.Arg725Cys)
NM_015346.4(ZFYVE26):c.2218C>T (p.His740Tyr)
NM_015346.4(ZFYVE26):c.2269T>C (p.Tyr757His) rs1555399213
NM_015346.4(ZFYVE26):c.2339G>A (p.Arg780Gln)
NM_015346.4(ZFYVE26):c.2495C>A (p.Pro832Gln)
NM_015346.4(ZFYVE26):c.3173G>A (p.Arg1058Gln)
NM_015346.4(ZFYVE26):c.3346G>T (p.Ala1116Ser) rs1566884500
NM_015346.4(ZFYVE26):c.3523G>A (p.Asp1175Asn)
NM_015346.4(ZFYVE26):c.443G>A (p.Arg148His) rs144919978
NM_015346.4(ZFYVE26):c.443G>C (p.Arg148Pro) rs144919978
NM_015346.4(ZFYVE26):c.5386G>A (p.Glu1796Lys)
NM_015346.4(ZFYVE26):c.5584C>T (p.Arg1862Cys)
NM_015346.4(ZFYVE26):c.6479A>T (p.Tyr2160Phe)
NM_015346.4(ZFYVE26):c.7081C>A (p.Pro2361Thr)
NM_015346.4(ZFYVE26):c.7348G>A (p.Ala2450Thr)

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