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: 22
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HGVS dbSNP gnomAD frequency
NM_006904.7(PRKDC):c.10301T>C (p.Ile3434Thr) rs7830743 0.13382
NM_006904.7(PRKDC):c.3759G>A (p.Thr1253=) rs8178087 0.02475
NM_006904.7(PRKDC):c.10211G>A (p.Gly3404Glu) rs8178225 0.01254
NM_006904.7(PRKDC):c.9145C>T (p.Leu3049=) rs56053523 0.00669
NM_006904.7(PRKDC):c.11805C>T (p.Gly3935=) rs8178249 0.00590
NM_006904.7(PRKDC):c.3042+18C>A rs56169650 0.00521
NM_006904.7(PRKDC):c.6480C>T (p.Tyr2160=) rs55991828 0.00408
NM_006904.7(PRKDC):c.9446G>A (p.Gly3149Asp) rs8178208 0.00320
NM_006904.7(PRKDC):c.9557+8G>A rs8178209 0.00313
NM_006904.7(PRKDC):c.10759-11T>C rs373043773 0.00266
NM_006904.7(PRKDC):c.4435G>C (p.Val1479Leu) rs199731143 0.00104
NM_006904.7(PRKDC):c.9933C>T (p.Asn3311=) rs201592874 0.00080
NM_006904.7(PRKDC):c.11698C>G (p.Leu3900Val) rs201214138 0.00057
NM_006904.7(PRKDC):c.7204C>T (p.Leu2402Phe) rs374403400 0.00051
NM_006904.7(PRKDC):c.3462G>A (p.Pro1154=) rs368215109 0.00020
NM_006904.7(PRKDC):c.4137C>T (p.Pro1379=) rs189680139 0.00011
NM_006904.7(PRKDC):c.10774G>T (p.Val3592Leu) rs1490966994 0.00006
NM_006904.7(PRKDC):c.594C>T (p.Arg198=) rs550250358 0.00005
NM_006904.7(PRKDC):c.11967G>A (p.Arg3989=) rs953043854 0.00001
NM_006904.7(PRKDC):c.4014G>A (p.Val1338=) rs976690996 0.00001
NM_006904.7(PRKDC):c.3848-14A>T rs749113047
NM_006904.7(PRKDC):c.9923-17dup rs573568510

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