ClinVar Miner

List of variants in gene PRDM5 reported as likely benign by GeneDx

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Gene type:
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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_018699.4(PRDM5):c.1444-186T>C rs1511302 0.04976
NM_018699.4(PRDM5):c.475+179T>C rs343185 0.04971
NM_018699.4(PRDM5):c.945+260T>A rs139976957 0.01788
NM_018699.4(PRDM5):c.177+208C>T rs138020106 0.01669
NM_018699.4(PRDM5):c.1283-123A>G rs114852145 0.01663
NM_018699.4(PRDM5):c.177+185C>T rs142701541 0.01362
NM_018699.4(PRDM5):c.*120T>C rs77157999 0.01181
NM_018699.4(PRDM5):c.1282+135C>T rs114415063 0.01143
NM_018699.4(PRDM5):c.1624-200C>T rs138821238 0.01018
NM_018699.4(PRDM5):c.744-110A>G rs73843619 0.00939
NM_018699.4(PRDM5):c.946-157G>A rs55847539 0.00939
NM_018699.4(PRDM5):c.866-181A>G rs188427518 0.00830
NM_018699.4(PRDM5):c.945+218G>A rs72921565 0.00478
NM_018699.4(PRDM5):c.946-101A>G rs72921557 0.00476
NM_018699.4(PRDM5):c.476-162T>C rs149691499 0.00397
NM_018699.4(PRDM5):c.1443+234A>C rs143076911 0.00364
NM_018699.4(PRDM5):c.1444-292A>G rs76835364 0.00342
NM_018699.4(PRDM5):c.1283-294G>A rs150447566 0.00335
NC_000004.12:g.120923147A>G rs189084602 0.00315
NM_018699.4(PRDM5):c.476-175_476-172del rs572645905 0.00259
NM_018699.4(PRDM5):c.651-97C>T rs143516568 0.00240
NM_018699.4(PRDM5):c.1283-5C>T rs185134294 0.00213
NM_018699.4(PRDM5):c.342A>C (p.Glu114Asp) rs146228268 0.00070
NM_018699.4(PRDM5):c.1633T>C (p.Tyr545His) rs142515463 0.00030
NM_018699.4(PRDM5):c.1031-15T>C rs201474353 0.00028
NM_018699.4(PRDM5):c.726C>T (p.Ser242=) rs372141288 0.00013
NM_018699.4(PRDM5):c.1282+9C>T rs79915407 0.00011
NM_018699.4(PRDM5):c.1722G>A (p.Gln574=) rs147796327 0.00009
NM_018699.4(PRDM5):c.252C>T (p.Phe84=) rs576918913 0.00009
NM_018699.4(PRDM5):c.300+17C>T rs376707809 0.00008
NM_018699.4(PRDM5):c.*4G>A rs746723307 0.00007
NM_018699.4(PRDM5):c.1282+17G>C rs199821555 0.00002
NM_018699.4(PRDM5):c.360G>T (p.Leu120=) rs751789550 0.00002
NM_018699.4(PRDM5):c.666A>G (p.Thr222=) rs748098382 0.00002
NM_018699.4(PRDM5):c.1188+13A>C rs748042897 0.00001
NM_018699.4(PRDM5):c.669G>A (p.Ala223=) rs754555498 0.00001
NM_018699.4(PRDM5):c.-34G>A rs1207928854
NM_018699.4(PRDM5):c.1282+12T>C rs908831002
NM_018699.4(PRDM5):c.1282+16G>A rs776670103
NM_018699.4(PRDM5):c.1444-58A>C rs72921539
NM_018699.4(PRDM5):c.1851C>T (p.Leu617=) rs767571327
NM_018699.4(PRDM5):c.237C>T (p.Ser79=) rs374500219
NM_018699.4(PRDM5):c.475+6G>C rs1367821206
NM_018699.4(PRDM5):c.651-21_651-20del rs756265026
NM_018699.4(PRDM5):c.93+16del rs1554014221
NM_018699.4(PRDM5):c.93+202C>T rs3761726
NM_018699.4(PRDM5):c.93+240C>A rs541636331
NM_018699.4(PRDM5):c.946-20_946-17del rs755237174
NM_018699.4(PRDM5):c.946-5del rs1578781216

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