ClinVar Miner

List of variants in gene MCM4 reported as benign for not provided

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_182746.3(MCM4):c.1948T>A (p.Leu650Met) rs762679 0.88261
NM_182746.3(MCM4):c.*358T>C rs17287761 0.04003
NM_182746.3(MCM4):c.*71C>A rs17334535 0.03423
NM_182746.3(MCM4):c.1174+20C>T rs6473933 0.02549
NM_182746.3(MCM4):c.*197T>C rs17334542 0.01714
NM_182746.3(MCM4):c.2064G>A (p.Lys688=) rs143488457 0.00503
NM_182746.3(MCM4):c.236-4A>G rs2305952 0.00339
NM_182746.3(MCM4):c.858C>T (p.Ser286=) rs17334388 0.00337
NM_182746.3(MCM4):c.1209A>G (p.Pro403=) rs17287656 0.00318
NM_182746.3(MCM4):c.1053+4C>T rs17334395 0.00313
NM_182746.3(MCM4):c.1659A>G (p.Thr553=) rs17287677 0.00313
NM_182746.3(MCM4):c.961C>T (p.Arg321Cys) rs142732823 0.00188
NM_182746.3(MCM4):c.598-10T>C rs143836714 0.00133
NM_182746.3(MCM4):c.833-14T>C rs191317744 0.00131
NM_182746.3(MCM4):c.1569G>A (p.Val523=) rs765660789 0.00109
NM_182746.3(MCM4):c.487A>G (p.Lys163Glu) rs34206069 0.00049
NM_182746.3(MCM4):c.1800+20G>A rs566442172 0.00011
NM_182746.3(MCM4):c.1929-6T>C rs567917422 0.00003
NM_182746.3(MCM4):c.1435-7del rs558445010
NM_182746.3(MCM4):c.1578C>T (p.Leu526=) rs34157149
NM_182746.3(MCM4):c.2082G>C (p.Ala694=) rs201709288
NM_182746.3(MCM4):c.2172G>A (p.Arg724=) rs367938513
NM_182746.3(MCM4):c.236-5del
NM_182746.3(MCM4):c.2366-8del rs2090994975
NM_182746.3(MCM4):c.598-5dup
NM_182746.3(MCM4):c.71-94C>T

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