ClinVar Miner

List of variants in gene MBD5 reported by Illumina Clinical Services Laboratory,Illumina

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Total variants: 51
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HGVS dbSNP
NM_018328.4(MBD5):c.*162dup rs879943522
NM_018328.4(MBD5):c.*200A>G rs16828708
NM_018328.4(MBD5):c.*229G>A rs886054915
NM_018328.4(MBD5):c.*283A>G rs148895172
NM_018328.4(MBD5):c.*288G>A rs886054916
NM_018328.4(MBD5):c.*299T>C rs561324330
NM_018328.4(MBD5):c.*405C>T rs185867776
NM_018328.4(MBD5):c.*526A>T rs886054917
NM_018328.4(MBD5):c.-224A>T rs886054906
NM_018328.4(MBD5):c.-296G>A rs886054905
NM_018328.4(MBD5):c.-457T>C rs146389489
NM_018328.4(MBD5):c.-556-8T>C rs140968376
NM_018328.4(MBD5):c.-573T>A rs886054904
NM_018328.4(MBD5):c.-591dup rs886054903
NM_018328.4(MBD5):c.-63C>G rs886054907
NM_018328.4(MBD5):c.-659T>C rs886054902
NM_018328.4(MBD5):c.-663C>T rs748989182
NM_018328.4(MBD5):c.-829A>G rs186186684
NM_018328.4(MBD5):c.-831+9dup rs796052705
NM_018328.4(MBD5):c.1111C>G (p.Gln371Glu) rs536900412
NM_018328.4(MBD5):c.113+8C>A rs886054908
NM_018328.4(MBD5):c.1368G>T (p.Ser456=) rs146020786
NM_018328.4(MBD5):c.1591A>G (p.Asn531Asp) rs757922781
NM_018328.4(MBD5):c.1596A>G (p.Val532=) rs114611333
NM_018328.4(MBD5):c.1602T>C (p.Asn534=) rs768359954
NM_018328.4(MBD5):c.1653A>G (p.Val551=) rs765225789
NM_018328.4(MBD5):c.1793A>G (p.Asn598Ser) rs774519380
NM_018328.4(MBD5):c.2030G>A (p.Ser677Asn) rs114314967
NM_018328.4(MBD5):c.2140C>G (p.His714Asp) rs886054909
NM_018328.4(MBD5):c.2277G>A (p.Val759=) rs750839601
NM_018328.4(MBD5):c.2301C>T (p.Asn767=) rs886054910
NM_018328.4(MBD5):c.2371G>A (p.Gly791Arg) rs769480362
NM_018328.4(MBD5):c.2454G>A (p.Thr818=) rs769275989
NM_018328.4(MBD5):c.2605G>A (p.Val869Ile) rs116207524
NM_018328.4(MBD5):c.274G>A (p.Ala92Thr) rs770801894
NM_018328.4(MBD5):c.2825T>C (p.Leu942Pro) rs886054911
NM_018328.4(MBD5):c.2974C>A (p.Leu992Ile) rs776251206
NM_018328.4(MBD5):c.2979G>C (p.Gln993His) rs148321416
NM_018328.4(MBD5):c.3044A>G (p.Gln1015Arg) rs143028540
NM_018328.4(MBD5):c.3055-9T>C rs370173652
NM_018328.4(MBD5):c.3152C>A (p.Pro1051His) rs761872951
NM_018328.4(MBD5):c.3253G>A (p.Val1085Ile) rs199626531
NM_018328.4(MBD5):c.3352C>T (p.Pro1118Ser) rs886054912
NM_018328.4(MBD5):c.3385T>C (p.Ser1129Pro) rs200395037
NM_018328.4(MBD5):c.3595G>A (p.Gly1199Arg) rs201334086
NM_018328.4(MBD5):c.3620G>A (p.Arg1207Gln) rs139042949
NM_018328.4(MBD5):c.398-12C>T rs556768118
NM_018328.4(MBD5):c.4038T>C (p.Asn1346=) rs147744781
NM_018328.4(MBD5):c.4221C>T (p.Asp1407=) rs768363712
NM_018328.4(MBD5):c.4432G>A (p.Gly1478Ser) rs886054913
NM_018328.4(MBD5):c.932A>C (p.Lys311Thr) rs200561241

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