ClinVar Miner

List of variants in gene UBIAD1 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_013319.3(UBIAD1):c.*612T>C rs886045071 0.00050
NM_013319.3(UBIAD1):c.*1189A>G rs776390306 0.00039
NM_013319.3(UBIAD1):c.*1265T>A rs372234308 0.00034
NM_013319.3(UBIAD1):c.*295G>A rs904203949 0.00030
NM_013319.3(UBIAD1):c.*1535A>T rs536904644 0.00019
NM_013319.3(UBIAD1):c.*1010C>T rs886045075 0.00016
NM_013319.3(UBIAD1):c.*519G>A rs937500463 0.00016
NM_013319.3(UBIAD1):c.*239G>A rs766089759 0.00013
NM_013319.3(UBIAD1):c.*1506T>C rs896437124 0.00011
NM_013319.3(UBIAD1):c.*234C>T rs1057311020 0.00008
NM_013319.3(UBIAD1):c.*709C>T rs752647371 0.00008
NM_013319.3(UBIAD1):c.*1580C>T rs961079383 0.00007
NM_013319.3(UBIAD1):c.*1876G>A rs959093111 0.00006
NM_013319.3(UBIAD1):c.*531C>A rs550736303 0.00006
NM_013319.3(UBIAD1):c.*675A>G rs376227906 0.00006
NM_013319.3(UBIAD1):c.751C>A (p.Leu251Ile) rs780282620 0.00006
NM_013319.3(UBIAD1):c.*1565G>A rs1028565043 0.00004
NM_013319.3(UBIAD1):c.*2201C>A rs897434247 0.00004
NM_013319.3(UBIAD1):c.*465_*466del rs777958656 0.00004
NM_013319.3(UBIAD1):c.*1495T>C rs886045080 0.00003
NM_013319.3(UBIAD1):c.*1719A>G rs886045082 0.00003
NM_013319.3(UBIAD1):c.*997C>T rs886045074 0.00003
NM_013319.3(UBIAD1):c.*1167C>T rs886045076 0.00001
NM_013319.3(UBIAD1):c.*1228A>G rs917463872 0.00001
NM_013319.3(UBIAD1):c.*1426C>T rs886045077 0.00001
NM_013319.3(UBIAD1):c.*1427T>C rs886045078 0.00001
NM_013319.3(UBIAD1):c.*1459T>A rs886045079 0.00001
NM_013319.3(UBIAD1):c.*1494A>G rs868102858 0.00001
NM_013319.3(UBIAD1):c.*1570G>A rs955630598 0.00001
NM_013319.3(UBIAD1):c.*170T>G rs1399081788 0.00001
NM_013319.3(UBIAD1):c.*2091G>A rs1235983002 0.00001
NM_013319.3(UBIAD1):c.*2115C>G rs886045085 0.00001
NM_013319.3(UBIAD1):c.*2187G>A rs886045086 0.00001
NM_013319.3(UBIAD1):c.*2213C>T rs760259916 0.00001
NM_013319.3(UBIAD1):c.*619A>G rs886045072 0.00001
NM_013319.3(UBIAD1):c.*847A>T rs886045073 0.00001
NM_013319.3(UBIAD1):c.-4T>C rs770112579 0.00001
NM_013319.3(UBIAD1):c.740C>T (p.Thr247Met) rs371649705 0.00001
NM_013319.3(UBIAD1):c.*1586C>T rs886045081
NM_013319.3(UBIAD1):c.*1779C>T rs886045083
NM_013319.3(UBIAD1):c.*1810del rs781564164
NM_013319.3(UBIAD1):c.*1811G>C rs867059451
NM_013319.3(UBIAD1):c.*221_*223del rs886045069
NM_013319.3(UBIAD1):c.*247T>C rs886045070
NM_013319.3(UBIAD1):c.*94G>A rs535726476
NM_013319.3(UBIAD1):c.*990T>C rs1638286979
NM_013319.3(UBIAD1):c.191C>T (p.Pro64Leu) rs1651875842
NM_013319.3(UBIAD1):c.494T>G (p.Phe165Cys) rs886045058
NM_013319.3(UBIAD1):c.600G>A (p.Met200Ile) rs773070987
NM_013319.3(UBIAD1):c.711G>T (p.Met237Ile) rs776301691
NM_013319.3(UBIAD1):c.739A>G (p.Thr247Ala) rs1638253298

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