ClinVar Miner

List of variants in gene MBD5 reported as uncertain significance for not specified

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Total variants: 19
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HGVS dbSNP
NM_018328.4(MBD5):c.1234G>A (p.Val412Ile) rs761118931
NM_018328.4(MBD5):c.1633T>C (p.Ser545Pro) rs775791197
NM_018328.4(MBD5):c.19T>A (p.Cys7Ser) rs766104877
NM_018328.4(MBD5):c.2173G>T (p.Ala725Ser) rs747127657
NM_018328.4(MBD5):c.2561A>G (p.Asn854Ser) rs1358383505
NM_018328.4(MBD5):c.2789A>C (p.Gln930Pro) rs564759063
NM_018328.4(MBD5):c.2978A>C (p.Gln993Pro) rs761395486
NM_018328.4(MBD5):c.3055-6T>C rs149825755
NM_018328.4(MBD5):c.3092G>T (p.Arg1031Ile) rs1553520435
NM_018328.4(MBD5):c.3367A>G (p.Met1123Val) rs1057518375
NM_018328.4(MBD5):c.3389T>C (p.Ile1130Thr) rs748142226
NM_018328.4(MBD5):c.3422G>A (p.Ser1141Asn) rs763106823
NM_018328.4(MBD5):c.3440G>A (p.Arg1147Gln) rs368605084
NM_018328.4(MBD5):c.3857G>A (p.Arg1286Lys) rs1057518363
NM_018328.4(MBD5):c.3972T>C (p.Ser1324=) rs765702142
NM_018328.4(MBD5):c.4158C>T (p.Gly1386=) rs543329958
NM_018328.4(MBD5):c.4316G>A (p.Arg1439His) rs150519311
NM_018328.4(MBD5):c.908T>G (p.Leu303Trp) rs797045689
NM_018328.4(MBD5):c.935A>T (p.Lys312Ile) rs146031838

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