ClinVar Miner

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

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_006904.7(PRKDC):c.1623+6A>G rs1231202 0.96352
NM_006904.7(PRKDC):c.12182+39G>A rs8178258 0.23073
NM_006904.7(PRKDC):c.5572-51G>A rs6993483 0.22999
NM_006904.7(PRKDC):c.10297+89G>C rs7828380 0.14596
NM_006904.7(PRKDC):c.10301T>C (p.Ile3434Thr) rs7830743 0.13382
NM_006904.7(PRKDC):c.8578-18G>T rs4873728 0.12075
NM_006904.7(PRKDC):c.967-71G>A rs8178016 0.12068
NM_006904.7(PRKDC):c.2934+5G>C rs8178060 0.05686
NM_006904.7(PRKDC):c.9922+13C>T rs8178217 0.05523
NM_006904.7(PRKDC):c.999G>A (p.Met333Ile) rs8178017 0.03099
NM_006904.7(PRKDC):c.1814C>G (p.Thr605Ser) rs8178033 0.02513
NM_006904.7(PRKDC):c.6346-105A>G rs8178148 0.01827
NM_006904.7(PRKDC):c.3212A>G (p.Asn1071Ser) rs8178070 0.01542
NM_006904.7(PRKDC):c.5088T>G (p.Leu1696=) rs6992074 0.01219
NM_006904.7(PRKDC):c.2083C>T (p.Pro695Ser) rs8178046 0.01166
NM_006904.7(PRKDC):c.10376A>G (p.Asn3459Ser) rs8178228 0.01084
NM_006904.7(PRKDC):c.9601C>T (p.Pro3201Ser) rs8178216 0.00825
NM_006904.7(PRKDC):c.4809G>T (p.Gln1603His) rs8178106 0.00109
NM_006904.7(PRKDC):c.2140-13_2140-11del rs370706897
NM_006904.7(PRKDC):c.325-19dup rs567466258

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