ClinVar Miner

List of variants in gene ALDOB reported by Eurofins NTD LLC (GA)

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Gene type:
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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_000035.4(ALDOB):c.-214G>A rs185972191 0.00678
NM_000035.4(ALDOB):c.448G>C (p.Ala150Pro) rs1800546 0.00319
NM_000035.4(ALDOB):c.156T>G (p.Thr52=) rs149671008 0.00302
NM_000035.4(ALDOB):c.799+6G>A rs141888548 0.00251
NM_000035.4(ALDOB):c.906T>C (p.Tyr302=) rs138866018 0.00151
NM_000035.4(ALDOB):c.324+8C>G rs118168553 0.00103
NM_000035.4(ALDOB):c.543T>G (p.Asn181Lys) rs35885472 0.00086
NM_000035.4(ALDOB):c.525C>T (p.Ala175=) rs144196914 0.00058
NM_000035.4(ALDOB):c.681C>T (p.Thr227=) rs61757689 0.00032
NM_000035.4(ALDOB):c.524C>A (p.Ala175Asp) rs76917243 0.00030
NM_000035.4(ALDOB):c.334G>A (p.Gly112Arg) rs373330514 0.00021
NM_000035.4(ALDOB):c.582T>C (p.Asp194=) rs141988626 0.00018
NM_000035.4(ALDOB):c.445C>T (p.Arg149Cys) rs190464963 0.00011
NM_000035.4(ALDOB):c.1013C>T (p.Ala338Val) rs77718928 0.00010
NM_000035.4(ALDOB):c.488C>T (p.Ala163Val) rs202210810 0.00009
NM_000035.4(ALDOB):c.590A>G (p.His197Arg) rs368140282 0.00008
NM_000035.4(ALDOB):c.991C>T (p.Arg331Trp) rs150407710 0.00007
NM_000035.4(ALDOB):c.1000-3T>C rs369238799 0.00006
NM_000035.4(ALDOB):c.226G>A (p.Gly76Ser) rs759204107 0.00006
NM_000035.4(ALDOB):c.401G>A (p.Arg134His) rs145252200 0.00004
NM_000035.4(ALDOB):c.853A>C (p.Asn285His) rs781725589 0.00004
NM_000035.4(ALDOB):c.128G>A (p.Arg43His) rs780442649 0.00003
NM_000035.4(ALDOB):c.760G>A (p.Val254Ile) rs776649110 0.00003
NM_000035.4(ALDOB):c.766G>T (p.Ala256Ser) rs201551409 0.00003
NM_000035.4(ALDOB):c.465C>T (p.Ala155=) rs569981883 0.00002
NM_000035.4(ALDOB):c.954T>C (p.Ala318=) rs572044496 0.00002
NM_000035.4(ALDOB):c.1014G>A (p.Ala338=) rs546735701 0.00001
NM_000035.4(ALDOB):c.136A>T (p.Arg46Trp) rs41281039 0.00001
NM_000035.4(ALDOB):c.179G>A (p.Arg60Gln) rs141267935 0.00001
NM_000035.4(ALDOB):c.489T>A (p.Ala163=) rs578048957 0.00001
NM_000035.4(ALDOB):c.538C>A (p.Gln180Lys) rs574635615 0.00001
NM_000035.4(ALDOB):c.599A>G (p.Glu200Gly) rs1564077843 0.00001
NM_000035.4(ALDOB):c.612T>A (p.Tyr204Ter) rs370793608 0.00001
NM_000035.4(ALDOB):c.952G>T (p.Ala318Ser) rs1364757729 0.00001
NM_000035.4(ALDOB):c.1005C>G (p.Asn335Lys) rs78340951
NM_000035.4(ALDOB):c.264C>A (p.Asp88Glu) rs200585150
NM_000035.4(ALDOB):c.302del (p.Lys101fs) rs974582114
NM_000035.4(ALDOB):c.360_363del (p.Asn120fs) rs387906225
NM_000035.4(ALDOB):c.428T>C (p.Val143Ala) rs896736761
NM_000035.4(ALDOB):c.476C>T (p.Pro159Leu) rs1564078173
NM_000035.4(ALDOB):c.485T>C (p.Leu162Pro) rs1564078167
NM_000035.4(ALDOB):c.487G>A (p.Ala163Thr) rs17852652
NM_000035.4(ALDOB):c.518G>A (p.Arg173His) rs756357123
NM_000035.4(ALDOB):c.529A>C (p.Ile177Leu) rs139442303
NM_000035.4(ALDOB):c.551T>C (p.Val184Ala) rs1554702550
NM_000035.4(ALDOB):c.759C>T (p.Thr253=) rs146360505
NM_000035.4(ALDOB):c.992G>A (p.Arg331Gln) rs371526091

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