ClinVar Miner

List of variants in gene ZBTB24 reported as uncertain significance for DNA repair disease

Included ClinVar conditions (97):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_014797.2(ZBTB24):c.109T>C (p.Cys37Arg) rs1562305271
NM_014797.2(ZBTB24):c.1154A>G (p.Lys385Arg) rs371071024
NM_014797.2(ZBTB24):c.1237C>T (p.Arg413Cys) rs149690823
NM_014797.2(ZBTB24):c.1322A>G (p.Lys441Arg)
NM_014797.2(ZBTB24):c.1597G>C (p.Val533Leu)
NM_014797.2(ZBTB24):c.1666G>A (p.Val556Ile) rs778110573
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) rs1222795316
NM_014797.2(ZBTB24):c.301G>A (p.Ala101Thr)
NM_014797.2(ZBTB24):c.334A>G (p.Thr112Ala)
NM_014797.2(ZBTB24):c.356A>G (p.Tyr119Cys)
NM_014797.2(ZBTB24):c.439G>T (p.Val147Leu) rs766594494
NM_014797.2(ZBTB24):c.730G>C (p.Glu244Gln) rs113516976
NM_014797.2(ZBTB24):c.762C>T (p.Ser254=)
NM_014797.2(ZBTB24):c.767G>A (p.Arg256Gln)
NM_014797.2(ZBTB24):c.784G>A (p.Val262Ile)
NM_014797.2(ZBTB24):c.788A>G (p.Lys263Arg)
NM_014797.2(ZBTB24):c.860A>G (p.Lys287Arg) rs1456427014
NM_014797.2(ZBTB24):c.883C>T (p.Arg295Cys)
NM_014797.2(ZBTB24):c.943A>G (p.Ser315Gly)

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