ClinVar Miner

List of variants in gene IVD reported as benign for classic organic aciduria

Included ClinVar conditions (39):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_002225.5(IVD):c.*1208G>A
NM_002225.5(IVD):c.*1471G>A rs4923865
NM_002225.5(IVD):c.*14C>T rs8040294
NM_002225.5(IVD):c.*1577C>G rs11630850
NM_002225.5(IVD):c.*1610C>T rs11630878
NM_002225.5(IVD):c.*1890G>C rs12185076
NM_002225.5(IVD):c.*1893del rs398026948
NM_002225.5(IVD):c.*195C>T rs77680513
NM_002225.5(IVD):c.*2070C>T rs187887699
NM_002225.5(IVD):c.*2275T>C rs11790
NM_002225.5(IVD):c.*2285C>G rs114657778
NM_002225.5(IVD):c.*261G>A rs2075624
NM_002225.5(IVD):c.*2844T>C rs7207
NM_002225.5(IVD):c.*2912G>A rs11557072
NM_002225.5(IVD):c.*3036del rs5812161
NM_002225.5(IVD):c.*447C>G rs79191320
NM_002225.5(IVD):c.*596G>A rs115034694
NM_002225.5(IVD):c.*808C>G rs2075625
NM_002225.5(IVD):c.*825C>A
NM_002225.5(IVD):c.-48G>A rs114259808
NM_002225.5(IVD):c.1066-5C>T rs115077254
NM_002225.5(IVD):c.1122C>T (p.Asp374=) rs372504234
NM_002225.5(IVD):c.229C>T (p.Leu77=) rs143807229
NM_002225.5(IVD):c.234+14T>C rs2289331
NM_002225.5(IVD):c.235-18G>A rs78272986
NM_002225.5(IVD):c.400A>G (p.Ile134Val) rs151118565
NM_002225.5(IVD):c.551-18C>T rs142064071
NM_002225.5(IVD):c.597C>T (p.Gly199=)
NM_002225.5(IVD):c.723C>T (p.Asp241=) rs2229312
NM_002225.5(IVD):c.88C>T (p.His30Tyr) rs73383128
NM_002225.5(IVD):c.891G>A (p.Ala297=) rs138427412

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