ClinVar Miner

List of variants in gene HDAC4 reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001378414.1(HDAC4):c.681C>T (p.His227=) rs148880349 0.00073
NM_001378414.1(HDAC4):c.3174C>T (p.Ala1058=) rs142279745 0.00053
NM_001378414.1(HDAC4):c.2190G>A (p.Thr730=) rs149067286 0.00036
NM_001378414.1(HDAC4):c.2661A>G (p.Thr887=) rs140526832 0.00032
NM_001378414.1(HDAC4):c.2151G>A (p.Gln717=) rs138137158 0.00022
NM_001378414.1(HDAC4):c.2346C>T (p.Cys782=) rs144099208 0.00010
NM_001378414.1(HDAC4):c.1358G>A (p.Arg453Gln) rs199784169 0.00006
NM_001378414.1(HDAC4):c.1649C>T (p.Pro550Leu) rs151167488 0.00006
NM_001378414.1(HDAC4):c.1434C>T (p.Asn478=) rs754530774 0.00005
NM_001378414.1(HDAC4):c.1458C>T (p.Val486=) rs139841625 0.00003
NM_001378414.1(HDAC4):c.865+8G>A rs778438043 0.00002
NM_001378414.1(HDAC4):c.922G>A (p.Gly308Arg) rs551711839 0.00002
NM_001378414.1(HDAC4):c.952C>T (p.Pro318Ser) rs886043422 0.00002
NM_001378414.1(HDAC4):c.2006A>G (p.Lys669Arg) rs886043528 0.00001
NM_001378414.1(HDAC4):c.2052C>T (p.Ala684=) rs754442298 0.00001
NM_001378414.1(HDAC4):c.339+10G>A rs199918439 0.00001
NM_001378414.1(HDAC4):c.1100C>T (p.Thr367Met) rs886043549
NM_001378414.1(HDAC4):c.2234-11dup rs775488590
NM_001378414.1(HDAC4):c.2434A>G (p.Ser812Gly) rs886044559
NM_001378414.1(HDAC4):c.571C>T (p.Leu191=) rs886044037

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.