ClinVar Miner

List of variants in gene ANKRD17 reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_032217.5(ANKRD17):c.332C>T (p.Thr111Ile) rs144971270 0.00102
NM_032217.5(ANKRD17):c.4576G>C (p.Glu1526Gln) rs748135097 0.00013
NM_032217.5(ANKRD17):c.3496G>A (p.Val1166Met) rs139919495 0.00012
NM_032217.5(ANKRD17):c.372C>G (p.Asp124Glu) rs748463495 0.00005
NM_032217.5(ANKRD17):c.6392C>T (p.Pro2131Leu) rs749174957 0.00005
NM_032217.5(ANKRD17):c.7175C>T (p.Ser2392Leu) rs201666060 0.00005
NM_032217.5(ANKRD17):c.6377C>G (p.Ser2126Cys) rs771817535 0.00002
NM_032217.5(ANKRD17):c.6574T>C (p.Ser2192Pro) rs1202915754 0.00002
NM_032217.5(ANKRD17):c.6974T>C (p.Met2325Thr) rs534030909 0.00002
NM_032217.5(ANKRD17):c.275G>C (p.Ser92Thr) rs569237927 0.00001
NM_032217.5(ANKRD17):c.7219G>A (p.Val2407Ile) rs748017210 0.00001
NM_032217.5(ANKRD17):c.213C>G (p.His71Gln)
NM_032217.5(ANKRD17):c.5035A>G (p.Ile1679Val) rs774552486
NM_032217.5(ANKRD17):c.5178G>A (p.Arg1726=)
NM_032217.5(ANKRD17):c.5485A>C (p.Asn1829His)
NM_032217.5(ANKRD17):c.6443C>T (p.Ala2148Val)
NM_032217.5(ANKRD17):c.7505G>A (p.Arg2502Gln)

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