ClinVar Miner

List of variants in gene PRDM5 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018699.4(PRDM5):c.1538-287T>G rs843559 0.99155
NM_018699.4(PRDM5):c.1188+309G>A rs1567552 0.86927
NM_018699.4(PRDM5):c.177+110G>A rs1901135 0.61482
NM_018699.4(PRDM5):c.1031-180A>G rs3789140 0.39138
NM_018699.4(PRDM5):c.865+320C>T rs2292395 0.38192
NM_018699.4(PRDM5):c.744-38C>T rs2136998 0.38181
NM_018699.4(PRDM5):c.681A>G (p.Leu227=) rs343192 0.28756
NM_018699.4(PRDM5):c.651-103G>A rs237212 0.28749
NM_018699.4(PRDM5):c.300+58A>G rs3115310 0.27262
NM_018699.4(PRDM5):c.945+274G>C rs3789142 0.25262
NM_018699.4(PRDM5):c.946-60G>C rs4833677 0.25248
NM_018699.4(PRDM5):c.476-150A>C rs343190 0.25243
NM_018699.4(PRDM5):c.946-41G>C rs4833676 0.25240
NM_018699.4(PRDM5):c.1537+144C>T rs3804163 0.21083
NM_018699.4(PRDM5):c.1443+287C>G rs4833674 0.20953
NM_018699.4(PRDM5):c.1283-239A>G rs55901892 0.20950
NM_018699.4(PRDM5):c.1283-176A>G rs56402218 0.20944
NM_018699.4(PRDM5):c.1188+115T>A rs12507359 0.20003
NM_018699.4(PRDM5):c.1030+232A>G rs2203060 0.19998
NM_018699.4(PRDM5):c.1234T>C (p.Leu412=) rs12499000 0.19996
NM_018699.4(PRDM5):c.1443+28A>G rs3761721 0.19943
NM_018699.4(PRDM5):c.1031-202A>C rs17415097 0.09329
NM_018699.4(PRDM5):c.1624-339T>C rs114750513 0.06807
NM_018699.4(PRDM5):c.1624-330C>T rs114245360 0.06668
NM_018699.4(PRDM5):c.651-225T>C rs17051265 0.05715
NM_018699.4(PRDM5):c.301-270C>T rs168226 0.05230
NM_018699.4(PRDM5):c.93+60A>G rs113037077 0.04980
NM_018699.4(PRDM5):c.1030+35C>A rs1511310 0.04584
NM_018699.4(PRDM5):c.849G>A (p.Gln283=) rs17051264 0.03566
NM_018699.4(PRDM5):c.660G>A (p.Gln220=) rs74320998 0.02419
NM_018699.4(PRDM5):c.1066T>A (p.Ser356Thr) rs140634372 0.01952
NM_018699.4(PRDM5):c.1728+286G>A rs79397936 0.01791
NM_018699.4(PRDM5):c.491A>T (p.Lys164Ile) rs146268537 0.01143
NM_018699.4(PRDM5):c.1383T>C (p.Tyr461=) rs55774575 0.00946
NM_018699.4(PRDM5):c.963T>C (p.Asp321=) rs34666716 0.00939
NM_018699.4(PRDM5):c.1273A>G (p.Ile425Val) rs75893420 0.00830
NM_018699.4(PRDM5):c.1632G>A (p.Pro544=) rs116026637 0.00299
NM_018699.4(PRDM5):c.1113C>A (p.Ser371Arg) rs148079992 0.00016
NM_018699.4(PRDM5):c.1030+45A>G rs1511309
NM_018699.4(PRDM5):c.1031-121del rs144058009
NM_018699.4(PRDM5):c.1031-6dup rs35363618
NM_018699.4(PRDM5):c.1189-151C>A rs75436862
NM_018699.4(PRDM5):c.1728+88_1728+89insTA rs71597093
NM_018699.4(PRDM5):c.177+123dup rs61156380
NM_018699.4(PRDM5):c.177+139del rs61156380
NM_018699.4(PRDM5):c.178-239G>A rs2597546
NM_018699.4(PRDM5):c.650+118del rs3840104
NM_018699.4(PRDM5):c.650+81TG[9] rs36062004
NM_018699.4(PRDM5):c.945+184dup rs3838231

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.