ClinVar Miner

List of variants in gene ARHGEF28 reported as benign by PreventionGenetics, part of Exact Sciences

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_001177693.2(ARHGEF28):c.1680A>G (p.Ser560=) rs2973568 0.67364
NM_001177693.2(ARHGEF28):c.945T>C (p.Ala315=) rs7716253 0.60447
NM_001177693.2(ARHGEF28):c.851C>A (p.Pro284Gln) rs6453022 0.55954
NM_001177693.2(ARHGEF28):c.673T>C (p.Trp225Arg) rs7714670 0.42107
NM_001177693.2(ARHGEF28):c.1024+12C>T rs2973548 0.41313
NM_001177693.2(ARHGEF28):c.4920T>A (p.His1640Gln) rs1478453 0.37320
NM_001177693.2(ARHGEF28):c.2283C>T (p.Gly761=) rs2931423 0.28939
NM_001177693.2(ARHGEF28):c.2338C>A (p.His780Asn) rs2973558 0.28922
NM_001177693.2(ARHGEF28):c.4948+11554C>T rs423333 0.28179
NM_001177693.2(ARHGEF28):c.1631C>T (p.Ser544Leu) rs2973571 0.23875
NM_001177693.2(ARHGEF28):c.1754G>A (p.Arg585Lys) rs2973566 0.23152
NM_001177693.2(ARHGEF28):c.964-7C>T rs73118524 0.19341
NM_001177693.2(ARHGEF28):c.3018C>T (p.Tyr1006=) rs3749645 0.13300
NM_001177693.2(ARHGEF28):c.823A>C (p.Arg275=) rs10473959 0.04709
NM_001177693.2(ARHGEF28):c.4622C>G (p.Ala1541Gly) rs78992879 0.03856
NM_001177693.2(ARHGEF28):c.3294T>C (p.Ala1098=) rs61734875 0.03735
NM_001177693.2(ARHGEF28):c.4642C>T (p.Pro1548Ser) rs17634865 0.03691
NM_001177693.2(ARHGEF28):c.4388G>A (p.Arg1463Gln) rs17634853 0.03585
NM_001177693.2(ARHGEF28):c.3753C>T (p.Asp1251=) rs146562116 0.01926
NM_001177693.2(ARHGEF28):c.267G>A (p.Val89=) rs17552682 0.00840
NM_001177693.2(ARHGEF28):c.1862G>A (p.Arg621Gln) rs115243197 0.00652
NM_001177693.2(ARHGEF28):c.4960T>C (p.Ser1654Pro) rs282414 0.00476
NM_001177693.2(ARHGEF28):c.1024+18212C>T
NM_001177693.2(ARHGEF28):c.2297+16= rs2931422
NM_001177693.2(ARHGEF28):c.4172C>A (p.Thr1391Asn)
NM_001177693.2(ARHGEF28):c.4358G>T (p.Arg1453Leu) rs139349480

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