ClinVar Miner

List of variants in gene MMAB studied for abdominal and pelvic region disorder

Included ClinVar conditions (891):
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Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NC_000012.12:g.(?_109561020)_(109565196_?)del
NM_052845.3(MMAB):c.107delG (p.Gly36Alafs) rs1555276160
NM_052845.3(MMAB):c.185C>T (p.Thr62Met) rs115802744
NM_052845.3(MMAB):c.197-1G>T rs763935916
NM_052845.3(MMAB):c.197-2delA rs1555275604
NM_052845.3(MMAB):c.197_290del94 rs864309511
NM_052845.3(MMAB):c.287T>C (p.Ile96Thr) rs864309509
NM_052845.3(MMAB):c.291-1G>A rs199971687
NM_052845.3(MMAB):c.316A>G (p.Lys106Glu) rs765917146
NM_052845.3(MMAB):c.349-3dup rs759049347
NM_052845.3(MMAB):c.349_354delATCCAG rs864309510
NM_052845.3(MMAB):c.373G>A (p.Gly125Ser) rs193015172
NM_052845.3(MMAB):c.377C>T (p.Ser126Leu) rs771053425
NM_052845.3(MMAB):c.37_54del18 (p.Gly13_Leu18del) rs770077320
NM_052845.3(MMAB):c.388_411del24 (p.Thr130_Glu137del) rs1555274650
NM_052845.3(MMAB):c.398C>T (p.Ser133Phe) rs749936057
NM_052845.3(MMAB):c.403G>A (p.Ala135Thr) rs35648932
NM_052845.3(MMAB):c.454G>T (p.Glu152Ter) rs557884699
NM_052845.3(MMAB):c.520_584del65 rs756195708
NM_052845.3(MMAB):c.521C>T (p.Ser174Leu) rs140881518
NM_052845.3(MMAB):c.541G>A (p.Ala181Thr)
NM_052845.3(MMAB):c.548A>T (p.His183Leu) rs752866643
NM_052845.3(MMAB):c.556C>T (p.Arg186Trp) rs28941784
NM_052845.3(MMAB):c.557G>A (p.Arg186Gln) rs773059864
NM_052845.3(MMAB):c.562G>A (p.Val188Met) rs768176676
NM_052845.3(MMAB):c.563T>G (p.Val188Gly) rs869320654
NM_052845.3(MMAB):c.563_577dupTGTGCCGCCGGGCCG (p.Ala192_Glu193insValCysArgArgAla) rs1555274496
NM_052845.3(MMAB):c.568C>T (p.Arg190Cys) rs398124434
NM_052845.3(MMAB):c.569G>A (p.Arg190His) rs756414548
NM_052845.3(MMAB):c.56_57delGCinsAA (p.Arg19Gln) rs36013132
NM_052845.3(MMAB):c.571C>T (p.Arg191Trp) rs376128990
NM_052845.3(MMAB):c.572G>A (p.Arg191Gln) rs746219370
NM_052845.3(MMAB):c.573_577delGGCCG (p.Ala192Glufs)
NM_052845.3(MMAB):c.573_577dup (p.Glu193Glyfs) rs1555274497
NM_052845.3(MMAB):c.577G>A (p.Glu193Lys) rs749758687
NM_052845.3(MMAB):c.577G>C (p.Glu193Gln) rs749758687
NM_052845.3(MMAB):c.578_584dup (p.Val196Glufs) rs1555274493
NM_052845.3(MMAB):c.583_584+18del20 rs1555274484
NM_052845.3(MMAB):c.584+14_584+33del20 rs1555274482
NM_052845.3(MMAB):c.585-2A>C rs1555274254
NM_052845.3(MMAB):c.656A>G (p.Tyr219Cys) rs765547005
NM_052845.3(MMAB):c.660_661delCT (p.Phe221Hisfs) rs1383825118
NM_052845.3(MMAB):c.700C>T (p.Gln234Ter) rs369296618
NM_052845.3(MMAB):c.716T>A (p.Met239Lys) rs9593
NM_052845.4(MMAB):c.570_572dup (p.Arg191_Ala192insArg) rs864309512

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