ClinVar Miner

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

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP
NM_003361.3(UMOD):c.*104C>T rs111699931
NM_003361.3(UMOD):c.*130C>T rs113468667
NM_003361.3(UMOD):c.*226_*229del rs886051782
NM_003361.3(UMOD):c.*231A>G rs886051781
NM_003361.3(UMOD):c.*59G>A rs886051783
NM_003361.3(UMOD):c.*88G>A rs547514548
NM_003361.3(UMOD):c.-14del rs764637746
NM_003361.3(UMOD):c.-1746T>C rs13333226
NM_003361.3(UMOD):c.-47T>C rs75645968
NM_003361.3(UMOD):c.-56G>A rs79245268
NM_003361.3(UMOD):c.1062C>T (p.Phe354=) rs78613713
NM_003361.3(UMOD):c.1131G>C (p.Trp377Cys) rs201738891
NM_003361.3(UMOD):c.1177T>C (p.Leu393=) rs748849021
NM_003361.3(UMOD):c.1182+5G>T rs755374625
NM_003361.3(UMOD):c.1372G>T (p.Val458Leu) rs55772253
NM_003361.3(UMOD):c.1375C>T (p.Arg459Trp) rs139607138
NM_003361.3(UMOD):c.1406C>T (p.Thr469Met) rs143583842
NM_003361.3(UMOD):c.1458C>T (p.Tyr486=) rs141800038
NM_003361.3(UMOD):c.1463G>A (p.Gly488Asp) rs1555486021
NM_003361.3(UMOD):c.1464C>T (p.Gly488=) rs141912637
NM_003361.3(UMOD):c.1500A>G (p.Ala500=) rs200895986
NM_003361.3(UMOD):c.1623G>T (p.Gly541=) rs562726925
NM_003361.3(UMOD):c.1680C>G (p.Asp560Glu) rs200473249
NM_003361.3(UMOD):c.1742C>A (p.Thr581Asn) rs143641292
NM_003361.3(UMOD):c.184A>C (p.Thr62Pro) rs143248111
NM_003361.3(UMOD):c.1859dup (p.Leu620fs) rs886051784
NM_003361.3(UMOD):c.1916T>C (p.Phe639Ser) rs145165861
NM_003361.3(UMOD):c.230G>A (p.Cys77Tyr) rs121917768
NM_003361.3(UMOD):c.264C>T (p.Gly88=) rs77875418
NM_003361.3(UMOD):c.278_289delinsCCGCCTCCT (p.Val93_Gly97delinsAlaAlaSerCys) rs878855325
NM_003361.3(UMOD):c.307G>T (p.Gly103Cys) rs28934584
NM_003361.3(UMOD):c.358T>G (p.Cys120Gly) rs1555487621
NM_003361.3(UMOD):c.376T>C (p.Cys126Arg) rs121917769
NM_003361.3(UMOD):c.383A>G (p.Asn128Ser) rs121917770
NM_003361.3(UMOD):c.425G>A (p.Arg142Gln) rs199835347
NM_003361.3(UMOD):c.443G>A (p.Cys148Tyr) rs28934582
NM_003361.3(UMOD):c.490G>T (p.Glu164Ter) rs1057515585
NM_003361.3(UMOD):c.522C>T (p.Cys174=) rs7193058
NM_003361.3(UMOD):c.529_555del (p.His177_Arg185del) rs1555487528
NM_003361.3(UMOD):c.538C>G (p.Leu180Val) rs187555378
NM_003361.3(UMOD):c.587A>G (p.Asp196Gly) rs1060499657
NM_003361.3(UMOD):c.649T>C (p.Cys217Arg) rs28934583
NM_003361.3(UMOD):c.649T>G (p.Cys217Gly) rs28934583
NM_003361.3(UMOD):c.743G>C (p.Cys248Ser) rs398122388
NM_003361.3(UMOD):c.764G>A (p.Cys255Tyr) rs121917771
NM_003361.3(UMOD):c.792G>A (p.Val264=) rs13335818
NM_003361.3(UMOD):c.817G>T (p.Val273Phe) rs121917774
NM_003361.3(UMOD):c.840C>T (p.Pro280=) rs78691203
NM_003361.3(UMOD):c.865+7C>G rs759063012
NM_003361.3(UMOD):c.885G>A (p.Gly295=) rs28544423
NM_003361.3(UMOD):c.898T>G (p.Cys300Gly) rs121917772
NM_003361.3(UMOD):c.943T>C (p.Cys315Arg) rs121917773
NM_003361.3(UMOD):c.947A>C (p.Gln316Pro) rs1555487318
NM_003361.3(UMOD):c.949T>G (p.Cys317Gly) rs1555487316
NM_003361.3(UMOD):c.974-15C>G rs201798915

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