ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_001378414.1(HDAC4):c.1692G>A (p.Lys564=) rs114495208 0.00604
NM_001378414.1(HDAC4):c.955G>A (p.Ala319Thr) rs76224543 0.00391
NM_001378414.1(HDAC4):c.958G>A (p.Val320Ile) rs73000144 0.00328
NM_001378414.1(HDAC4):c.1953C>T (p.Pro651=) rs146056747 0.00292
NM_001378414.1(HDAC4):c.1095+10C>G rs11896634 0.00291
NM_001378414.1(HDAC4):c.1809G>A (p.Glu603=) rs148813865 0.00231
NM_001378414.1(HDAC4):c.684G>A (p.Pro228=) rs144387989 0.00183
NM_001378414.1(HDAC4):c.2371G>A (p.Ala791Thr) rs61754648 0.00181
NM_001378414.1(HDAC4):c.2163G>A (p.Ser721=) rs61735030 0.00180
NM_001378414.1(HDAC4):c.222G>A (p.Glu74=) rs145137674 0.00180
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.1978+8G>A rs200120991 0.00014
NM_001378414.1(HDAC4):c.1101G>A (p.Thr367=) rs371792033 0.00013
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.567G>A (p.Arg189=) rs141942329
NM_001378414.1(HDAC4):c.571C>T (p.Leu191=) rs886044037

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