ClinVar Miner

List of variants in gene PRKDC reported as uncertain significance for not provided

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Total variants: 20
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HGVS dbSNP
NM_001081640.2(PRKDC):c.2667G>C (p.Glu889Asp) rs200126714
NM_006904.6(PRKDC):c.11029C>T (p.Pro3677Ser) rs55924155
NM_006904.6(PRKDC):c.1114-1G>A rs1554645438
NM_006904.6(PRKDC):c.11713G>T (p.Ala3905Ser) rs762000221
NM_006904.6(PRKDC):c.11978C>T (p.Ser3993Leu) rs1554623574
NM_006904.6(PRKDC):c.1971T>C (p.Ser657=) rs766026632
NM_006904.6(PRKDC):c.2955G>C (p.Glu985Asp) rs202016860
NM_006904.6(PRKDC):c.3256T>C (p.Tyr1086His) rs1030128713
NM_006904.6(PRKDC):c.3709G>A (p.Ala1237Thr) rs191531119
NM_006904.6(PRKDC):c.3744C>T (p.Phe1248=) rs200729621
NM_006904.6(PRKDC):c.4009G>A (p.Val1337Ile) rs56080897
NM_006904.6(PRKDC):c.5120T>A (p.Leu1707Gln) rs202110076
NM_006904.6(PRKDC):c.5269A>G (p.Met1757Val) rs376292677
NM_006904.6(PRKDC):c.5559C>T (p.Ser1853=) rs777811841
NM_006904.6(PRKDC):c.5960G>A (p.Arg1987His) rs551812114
NM_006904.6(PRKDC):c.7114C>T (p.Pro2372Ser) rs748925420
NM_006904.6(PRKDC):c.7833C>T (p.Ala2611=) rs375277772
NM_006904.7(PRKDC):c.2755C>T (p.Leu919Phe)
NM_006904.7(PRKDC):c.3911A>G (p.His1304Arg) rs1315944028
NM_006904.7(PRKDC):c.9936_9937del (p.Ser3313fs) rs1589705455

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