ClinVar Miner

List of variants in gene MMAB reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_052845.4(MMAB):c.348+105T>C rs10850380 0.58164
NM_052845.4(MMAB):c.584+254A>G rs2058805 0.58162
NM_052845.4(MMAB):c.716T>A (p.Met239Lys) rs9593 0.57816
NM_052845.4(MMAB):c.645-156T>C rs888192 0.57808
NM_052845.4(MMAB):c.*1230G>T rs11067231 0.57792
NM_052845.4(MMAB):c.*857G>C rs877710 0.57567
NM_052845.4(MMAB):c.134+286T>C rs12314392 0.48699
NM_052845.4(MMAB):c.348+147G>A rs10850379 0.40515
NM_052845.4(MMAB):c.*2701G>C rs2241201 0.33323
NM_052845.4(MMAB):c.290+63T>C rs11836136 0.32654
NM_052845.4(MMAB):c.135-241T>C rs12322541 0.32362
NM_052845.4(MMAB):c.*3148G>A rs11067227 0.24433
NM_052845.4(MMAB):c.*625G>C rs11067233 0.24420
NM_052845.4(MMAB):c.*891C>A rs877709 0.24416
NM_052845.4(MMAB):c.349-207A>G rs11067271 0.18342
NM_052845.4(MMAB):c.*1535G>A rs34921355 0.17160
NM_052845.4(MMAB):c.*2835T>C rs12817689 0.17090
NM_052845.4(MMAB):c.519+157C>T rs2287180 0.17065
NM_052845.4(MMAB):c.520-128C>T rs2287181 0.17054
NM_052845.4(MMAB):c.520-96C>T rs11610545 0.17048
NM_052845.4(MMAB):c.*2684G>C rs35145546 0.16925
NM_052845.4(MMAB):c.644+212C>T rs35072126 0.16920
NM_052845.4(MMAB):c.520-139G>A rs12309115 0.11426
NM_052845.4(MMAB):c.645-247G>A rs12828717 0.11313
NM_052845.4(MMAB):c.585-204G>A rs2287182 0.10962
NM_052845.4(MMAB):c.*1467C>T rs1061440 0.10807
NM_052845.4(MMAB):c.*192T>C rs8228 0.10802
NM_052845.4(MMAB):c.*1952T>C rs61940463 0.10789
NM_052845.4(MMAB):c.*1810G>A rs73414076 0.10702
NM_052845.4(MMAB):c.*721T>G rs11831226 0.09002
NM_052845.4(MMAB):c.585-174G>A rs2287183 0.08550
NM_052845.4(MMAB):c.*378T>A rs66497319 0.08528
NM_052845.4(MMAB):c.348+177C>T rs61940511 0.08338
NM_052845.4(MMAB):c.584+24A>G rs78599682 0.07555
NM_052845.4(MMAB):c.*656C>A rs11067232 0.06631
NM_052845.4(MMAB):c.*1729A>C rs559163901 0.06120
NM_052845.4(MMAB):c.*376T>A rs527861371 0.05729
NM_052845.4(MMAB):c.585-262G>A rs72650185 0.05447
NM_052845.4(MMAB):c.*1005A>G rs67432283 0.05428
NM_052845.4(MMAB):c.196+279A>C rs72651703 0.05426
NM_052845.4(MMAB):c.584+251G>A rs68153744 0.05424
NM_052845.4(MMAB):c.135-23T>C rs66580225 0.05340
NM_052845.4(MMAB):c.*1657G>A rs111869218 0.05172
NM_052845.4(MMAB):c.644+213G>A rs112082462 0.05154
NM_052845.4(MMAB):c.290+204C>T rs113284916 0.04200
NM_052845.4(MMAB):c.*3178C>A rs73414071 0.02490
NM_052845.4(MMAB):c.*2628C>T rs73414074 0.02477
NM_052845.4(MMAB):c.*564G>C rs56760240 0.02466
NM_052845.4(MMAB):c.*374T>A rs549601416 0.02435
NM_052845.4(MMAB):c.585-203T>C rs74581509 0.01734
NM_052845.4(MMAB):c.*380A>T rs74967596 0.01505
NM_052845.4(MMAB):c.349-17T>C rs72650187 0.00583
NM_052845.4(MMAB):c.403G>A (p.Ala135Thr) rs35648932 0.00272
NM_052845.4(MMAB):c.135-38dup rs140204601 0.00165
NM_052845.4(MMAB):c.624C>T (p.Asn208=) rs146687452 0.00146
NM_052845.4(MMAB):c.394T>C (p.Cys132Arg) rs147457956 0.00085
NM_052845.4(MMAB):c.444G>A (p.Gly148=) rs117269384 0.00014
NM_052845.4(MMAB):c.197-146C>A rs12830693
NM_052845.4(MMAB):c.291-16del
NM_052845.4(MMAB):c.349-8dup rs759049347

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