ClinVar Miner

List of variants in gene TNK2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_001382273.1(TNK2):c.1029C>T (p.Ile343=) rs55842111 0.00892
NM_001382273.1(TNK2):c.2208G>A (p.Pro736=) rs62283329 0.00625
NM_001382273.1(TNK2):c.93C>T (p.Asn31=) rs56190948 0.00491
NM_001382273.1(TNK2):c.1872G>A (p.Thr624=) rs144161756 0.00306
NM_001382273.1(TNK2):c.1610G>T (p.Ser537Ile) rs143787673 0.00098
NM_001382273.1(TNK2):c.2140A>G (p.Ser714Gly) rs139797100 0.00035
NM_001382273.1(TNK2):c.1741G>C (p.Ala581Pro) rs202068965 0.00029
NM_001382273.1(TNK2):c.1809C>G (p.Ser603=) rs748303339 0.00006
NM_001382273.1(TNK2):c.843C>T (p.Asp281=) rs776183942 0.00001
NM_001382273.1(TNK2):c.-18-3798G>C
NM_001382273.1(TNK2):c.-18-3821G>A
NM_001382273.1(TNK2):c.-18-3877G>A
NM_001382273.1(TNK2):c.1488C>T (p.Leu496=)
NM_001382273.1(TNK2):c.1536G>A (p.Gly512=)
NM_001382273.1(TNK2):c.1680G>T (p.Gly560=)
NM_001382273.1(TNK2):c.1761C>T (p.Asp587=)
NM_001382273.1(TNK2):c.1821G>A (p.Leu607=)
NM_001382273.1(TNK2):c.1957G>A (p.Val653Met) rs201407161
NM_001382273.1(TNK2):c.2385G>A (p.Pro795=)
NM_001382273.1(TNK2):c.2713G>A (p.Val905Met) rs148323328
NM_001382273.1(TNK2):c.2778G>A (p.Pro926=)
NM_001382273.1(TNK2):c.305C>T (p.Ser102Leu)

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