ClinVar Miner

List of variants in gene PRKDC reported as likely benign for not specified

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Gene type:
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Total variants: 28
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HGVS dbSNP
NM_006904.6(PRKDC):c.-29G>A rs1057522893
NM_006904.6(PRKDC):c.10211G>A (p.Gly3404Glu) rs8178225
NM_006904.6(PRKDC):c.10626C>T (p.Phe3542=) rs8178231
NM_006904.6(PRKDC):c.10684T>A (p.Leu3562Met) rs8178232
NM_006904.6(PRKDC):c.10759-11T>C rs373043773
NM_006904.6(PRKDC):c.10774G>T (p.Val3592Leu) rs1490966994
NM_006904.6(PRKDC):c.11805C>T (p.Gly3935=) rs8178249
NM_006904.6(PRKDC):c.11967G>A (p.Arg3989=) rs953043854
NM_006904.6(PRKDC):c.3042+18C>A rs56169650
NM_006904.6(PRKDC):c.3462G>A (p.Pro1154=) rs368215109
NM_006904.6(PRKDC):c.3709G>A (p.Ala1237Thr) rs191531119
NM_006904.6(PRKDC):c.3759G>A (p.Thr1253=) rs8178087
NM_006904.6(PRKDC):c.3848-14A>T rs749113047
NM_006904.6(PRKDC):c.4014G>A (p.Val1338=) rs976690996
NM_006904.6(PRKDC):c.4137C>T (p.Pro1379=) rs189680139
NM_006904.6(PRKDC):c.42G>A (p.Arg14=) rs564283387
NM_006904.6(PRKDC):c.4435G>C (p.Val1479Leu) rs199731143
NM_006904.6(PRKDC):c.5571+5C>T rs780022870
NM_006904.6(PRKDC):c.594C>T (p.Arg198=) rs550250358
NM_006904.6(PRKDC):c.6480C>T (p.Tyr2160=) rs55991828
NM_006904.6(PRKDC):c.8661C>T (p.Pro2887=) rs78163867
NM_006904.6(PRKDC):c.9145C>T (p.Leu3049=) rs56053523
NM_006904.6(PRKDC):c.9217C>T (p.Leu3073Phe) rs55644332
NM_006904.6(PRKDC):c.9446G>A (p.Gly3149Asp) rs8178208
NM_006904.6(PRKDC):c.9557+8G>A rs8178209
NM_006904.6(PRKDC):c.9601C>T (p.Pro3201Ser) rs8178216
NM_006904.6(PRKDC):c.9933C>T (p.Asn3311=) rs201592874
NM_006904.7(PRKDC):c.9923-17dup rs573568510

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