ClinVar Miner

List of variants in gene MBD5 reported as likely benign for Mental retardation, autosomal dominant 1

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Total variants: 30
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HGVS dbSNP
NM_018328.4(MBD5):c.1382G>A (p.Arg461His) rs139964770
NM_018328.4(MBD5):c.1536C>T (p.Ser512=) rs147908860
NM_018328.4(MBD5):c.1537G>A (p.Asp513Asn) rs1465733702
NM_018328.4(MBD5):c.1589G>A (p.Ser530Asn) rs558138423
NM_018328.4(MBD5):c.1842T>C (p.Thr614=) rs1553518662
NM_018328.4(MBD5):c.1920T>C (p.Gly640=) rs1031744379
NM_018328.4(MBD5):c.1961A>T (p.Asp654Val) rs115495710
NM_018328.4(MBD5):c.1962C>T (p.Asp654=) rs139953766
NM_018328.4(MBD5):c.1999T>C (p.Leu667=) rs529715710
NM_018328.4(MBD5):c.2030G>A (p.Ser677Asn) rs114314967
NM_018328.4(MBD5):c.2170G>A (p.Gly724Arg) rs1553518717
NM_018328.4(MBD5):c.236G>A (p.Gly79Glu) rs34995577
NM_018328.4(MBD5):c.2519-8C>T rs761957089
NM_018328.4(MBD5):c.2520C>T (p.Gly840=) rs201649831
NM_018328.4(MBD5):c.2605G>A (p.Val869Ile) rs116207524
NM_018328.4(MBD5):c.267T>C (p.Asp89=) rs143333632
NM_018328.4(MBD5):c.2689G>A (p.Ala897Thr) rs778516851
NM_018328.4(MBD5):c.3027C>T (p.Pro1009=) rs144464864
NM_018328.4(MBD5):c.3044A>G (p.Gln1015Arg) rs143028540
NM_018328.4(MBD5):c.3183G>A (p.Pro1061=) rs752275705
NM_018328.4(MBD5):c.3702C>T (p.Val1234=) rs144957555
NM_018328.4(MBD5):c.384C>T (p.Pro128=) rs753595652
NM_018328.4(MBD5):c.3867C>T (p.His1289=) rs1354346236
NM_018328.4(MBD5):c.3896G>A (p.Arg1299Gln) rs35934694
NM_018328.4(MBD5):c.4101A>G (p.Pro1367=) rs1553520655
NM_018328.4(MBD5):c.4146G>A (p.Thr1382=) rs759890387
NM_018328.4(MBD5):c.4236A>C (p.Ser1412=) rs149419174
NM_018328.4(MBD5):c.675G>A (p.Ala225=) rs775582219
NM_018328.4(MBD5):c.924A>C (p.Pro308=) rs778385281
NM_018328.4(MBD5):c.974G>A (p.Arg325Gln) rs374866920

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