ClinVar Miner

List of variants in gene ALDH7A1 reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP
NM_001182.4(ALDH7A1):c.-117G>T rs146562077
NM_001182.4(ALDH7A1):c.-132A>C rs900641
NM_001182.4(ALDH7A1):c.-151C>T rs900640
NM_001182.4(ALDH7A1):c.-29T>C rs556650006
NM_001182.4(ALDH7A1):c.-60G>A rs144272515
NM_001182.4(ALDH7A1):c.-80T>G rs563928852
NM_001182.5(ALDH7A1):c.*1368A>T rs115645125
NM_001182.5(ALDH7A1):c.*1441C>T rs541286622
NM_001182.5(ALDH7A1):c.*1484T>C rs886059841
NM_001182.5(ALDH7A1):c.*1496T>A rs886059840
NM_001182.5(ALDH7A1):c.*1529A>G rs886059839
NM_001182.5(ALDH7A1):c.*1672A>G rs78029541
NM_001182.5(ALDH7A1):c.*1693A>C rs557939339
NM_001182.5(ALDH7A1):c.*1702del rs5871218
NM_001182.5(ALDH7A1):c.*1730C>T rs185960737
NM_001182.5(ALDH7A1):c.*1741T>A rs744720
NM_001182.5(ALDH7A1):c.*1748T>A rs744721
NM_001182.5(ALDH7A1):c.*1748_*1749delinsAT rs386692155
NM_001182.5(ALDH7A1):c.*1749G>T rs744722
NM_001182.5(ALDH7A1):c.*1804C>T rs744723
NM_001182.5(ALDH7A1):c.*1836C>A rs763990036
NM_001182.5(ALDH7A1):c.*1839G>A rs886059838
NM_001182.5(ALDH7A1):c.*2126G>A rs115168957
NM_001182.5(ALDH7A1):c.*2254T>A rs76249070
NM_001182.5(ALDH7A1):c.*2314T>C rs561998848
NM_001182.5(ALDH7A1):c.*2365C>T rs886059837
NM_001182.5(ALDH7A1):c.*2387A>G rs116566135
NM_001182.5(ALDH7A1):c.*2409A>C rs776633516
NM_001182.5(ALDH7A1):c.*2423C>T rs114575585
NM_001182.5(ALDH7A1):c.*2464dup rs200155555
NM_001182.5(ALDH7A1):c.*2492C>T rs768166252
NM_001182.5(ALDH7A1):c.*2499G>A rs7715516
NM_001182.5(ALDH7A1):c.*2512G>A rs76363408
NM_001182.5(ALDH7A1):c.*2549G>C rs556404419
NM_001182.5(ALDH7A1):c.*2568_*2569dup rs771970643
NM_001182.5(ALDH7A1):c.*2584C>A rs886059836
NM_001182.5(ALDH7A1):c.*2700A>T rs886059835
NM_001182.5(ALDH7A1):c.*2781C>T rs886059834
NM_001182.5(ALDH7A1):c.*2818T>C rs886059833
NM_001182.5(ALDH7A1):c.*2820dup rs886059832
NM_001182.5(ALDH7A1):c.*2996_*2997dup rs5871217
NM_001182.5(ALDH7A1):c.*2997dup rs5871217
NM_001182.5(ALDH7A1):c.*3022T>C rs2035471
NM_001182.5(ALDH7A1):c.*3124A>G rs572425402
NM_001182.5(ALDH7A1):c.*403C>T rs112493228
NM_001182.5(ALDH7A1):c.*404G>A rs533678440
NM_001182.5(ALDH7A1):c.*409del rs556732113
NM_001182.5(ALDH7A1):c.*548C>T rs1060856
NM_001182.5(ALDH7A1):c.*641G>A rs372065850
NM_001182.5(ALDH7A1):c.*65G>A rs886059848
NM_001182.5(ALDH7A1):c.*68A>G rs2775
NM_001182.5(ALDH7A1):c.*690T>C rs139905907
NM_001182.5(ALDH7A1):c.*717G>A rs886059847
NM_001182.5(ALDH7A1):c.*726C>T rs1060857
NM_001182.5(ALDH7A1):c.*807C>G rs1807
NM_001182.5(ALDH7A1):c.*818G>A rs1138005
NM_001182.5(ALDH7A1):c.*898_*900del rs543290589
NM_001182.5(ALDH7A1):c.1008+11C>T rs367574304
NM_001182.5(ALDH7A1):c.119C>T (p.Ala40Val) rs745385277
NM_001182.5(ALDH7A1):c.1234A>G (p.Thr412Ala) rs2306618
NM_001182.5(ALDH7A1):c.1279G>C (p.Glu427Gln) rs121912707
NM_001182.5(ALDH7A1):c.1315A>C (p.Lys439Gln) rs12514417
NM_001182.5(ALDH7A1):c.1406G>A (p.Arg469His) rs147940248
NM_001182.5(ALDH7A1):c.141_142insA (p.Arg48fs) rs1296037862
NM_001182.5(ALDH7A1):c.1439T>C (p.Ile480Thr) rs886059849
NM_001182.5(ALDH7A1):c.1567A>G (p.Thr523Ala) rs61757684
NM_001182.5(ALDH7A1):c.244del (p.Gln82fs) rs1317880376
NM_001182.5(ALDH7A1):c.273T>C (p.Thr91=) rs60720055
NM_001182.5(ALDH7A1):c.313-15G>A rs201720741
NM_001182.5(ALDH7A1):c.373A>G (p.Ile125Val) rs117295656
NM_001182.5(ALDH7A1):c.394-15G>A rs766287925
NM_001182.5(ALDH7A1):c.518-12T>G rs79544459
NM_001182.5(ALDH7A1):c.518-8G>A rs886059850
NM_001182.5(ALDH7A1):c.615C>T (p.Asn205=) rs369380330
NM_001182.5(ALDH7A1):c.675C>T (p.Leu225=) rs57902950

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