ClinVar Miner

List of variants in gene ZBTB24 studied for DNA repair disease

Included ClinVar conditions (95):
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Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP
NM_014797.2(ZBTB24):c.109T>C (p.Cys37Arg)
NM_014797.2(ZBTB24):c.1154A>G (p.Lys385Arg) rs371071024
NM_014797.2(ZBTB24):c.1204+5G>A rs80351559
NM_014797.2(ZBTB24):c.1222T>G (p.Cys408Gly) rs387907105
NM_014797.2(ZBTB24):c.1237C>T (p.Arg413Cys) rs149690823
NM_014797.2(ZBTB24):c.1289-11_1289-6delGTTTTT rs765964812
NM_014797.2(ZBTB24):c.135T>C (p.Asn45=) rs374383327
NM_014797.2(ZBTB24):c.1369C>T (p.Arg457Ter) rs387907106
NM_014797.2(ZBTB24):c.1389C>G (p.Ser463=) rs2232447
NM_014797.2(ZBTB24):c.146G>A (p.Arg49Gln) rs147441359
NM_014797.2(ZBTB24):c.14C>T (p.Ser5Leu) rs192918926
NM_014797.2(ZBTB24):c.1552G>A (p.Ala518Thr) rs2232448
NM_014797.2(ZBTB24):c.1597G>C (p.Val533Leu)
NM_014797.2(ZBTB24):c.1666G>A (p.Val556Ile) rs778110573
NM_014797.2(ZBTB24):c.1672G>A (p.Asp558Asn) rs61731736
NM_014797.2(ZBTB24):c.1688T>C (p.Ile563Thr) rs142830104
NM_014797.2(ZBTB24):c.1701C>T (p.Pro567=) rs2232449
NM_014797.2(ZBTB24):c.1750A>T (p.Met584Leu) rs139491074
NM_014797.2(ZBTB24):c.1811A>G (p.Asn604Ser)
NM_014797.2(ZBTB24):c.1969G>A (p.Glu657Lys)
NM_014797.2(ZBTB24):c.235C>T (p.Leu79=) rs746668886
NM_014797.2(ZBTB24):c.301G>A (p.Ala101Thr)
NM_014797.2(ZBTB24):c.439G>T (p.Val147Leu) rs766594494
NM_014797.2(ZBTB24):c.51C>T (p.Asp17=) rs376284623
NM_014797.2(ZBTB24):c.579G>A (p.Gln193=) rs2227263
NM_014797.2(ZBTB24):c.730G>C (p.Glu244Gln) rs113516976
NM_014797.2(ZBTB24):c.767G>A (p.Arg256Gln)
NM_014797.2(ZBTB24):c.784G>A (p.Val262Ile)
NM_014797.2(ZBTB24):c.860A>G (p.Lys287Arg) rs1456427014
NM_014797.2(ZBTB24):c.958C>T (p.Arg320Ter) rs387907104
ZBTB24, 2-BP DEL, 396TA
ZBTB24, SER16TER
ZBTB24, SER278TER

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