ClinVar Miner

List of variants in gene PRDM5 reported as uncertain significance by GeneDx

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_018699.4(PRDM5):c.1339T>A (p.Leu447Ile) rs193201534 0.00016
NM_018699.4(PRDM5):c.1114G>A (p.Glu372Lys) rs369580755 0.00014
NM_018699.4(PRDM5):c.248G>A (p.Arg83His) rs201945549 0.00012
NM_018699.4(PRDM5):c.508C>T (p.Pro170Ser) rs746068577 0.00012
NM_018699.4(PRDM5):c.544C>T (p.Leu182Phe) rs199602365 0.00011
NM_018699.4(PRDM5):c.1031-6T>A rs753768741 0.00010
NM_018699.4(PRDM5):c.6G>T (p.Leu2=) rs745891819 0.00008
NM_018699.4(PRDM5):c.740C>T (p.Ser247Leu) rs187637689 0.00006
NM_018699.4(PRDM5):c.839A>G (p.Lys280Arg) rs183142477 0.00004
NM_018699.4(PRDM5):c.1741G>A (p.Ala581Thr) rs759782529 0.00003
NM_018699.4(PRDM5):c.650+5G>A rs754469516 0.00003
NM_018699.4(PRDM5):c.1613C>T (p.Thr538Ile) rs140622920 0.00002
NM_018699.4(PRDM5):c.842G>T (p.Arg281Ile) rs373835306 0.00002
NM_018699.4(PRDM5):c.125A>C (p.Lys42Thr) rs1269597260 0.00001
NM_018699.4(PRDM5):c.1406C>T (p.Ala469Val) rs757433292 0.00001
NM_018699.4(PRDM5):c.1550A>G (p.Tyr517Cys) rs763317084 0.00001
NM_018699.4(PRDM5):c.1847A>G (p.Tyr616Cys) rs928901991 0.00001
NM_018699.4(PRDM5):c.692C>T (p.Ser231Leu) rs750031024 0.00001
NM_018699.4(PRDM5):c.86T>A (p.Val29Glu) rs1281285547 0.00001
NM_018699.4(PRDM5):c.1208C>T (p.Pro403Leu)
NM_018699.4(PRDM5):c.1241G>T (p.Arg414Leu) rs753113187
NM_018699.4(PRDM5):c.1697C>T (p.Thr566Met)
NM_018699.4(PRDM5):c.1862T>C (p.Met621Thr)
NM_018699.4(PRDM5):c.310A>G (p.Asn104Asp) rs887320638
NM_018699.4(PRDM5):c.676A>T (p.Ser226Cys) rs1754592780

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