ClinVar Miner

List of variants in gene LOXHD1 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 101
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HGVS dbSNP
NM_144612.6(LOXHD1):c.*124A>G rs144543819
NM_144612.6(LOXHD1):c.*19C>T rs778387862
NM_144612.6(LOXHD1):c.*73A>T rs748582582
NM_144612.6(LOXHD1):c.*96G>A rs569671846
NM_144612.6(LOXHD1):c.1191G>T (p.Trp397Cys) rs201033524
NM_144612.6(LOXHD1):c.1303G>A (p.Asp435Asn) rs561064266
NM_144612.6(LOXHD1):c.1431+10G>T rs57330753
NM_144612.6(LOXHD1):c.1459T>C (p.Tyr487His) rs886053839
NM_144612.6(LOXHD1):c.1476G>T (p.Trp492Cys) rs369682197
NM_144612.6(LOXHD1):c.1500T>C (p.Ser500=) rs886053838
NM_144612.6(LOXHD1):c.1571G>A (p.Arg524His) rs187658135
NM_144612.6(LOXHD1):c.1617G>A (p.Met539Ile) rs143142227
NM_144612.6(LOXHD1):c.1714A>C (p.Asn572His) rs886053837
NM_144612.6(LOXHD1):c.1716C>T (p.Asn572=) rs147582935
NM_144612.6(LOXHD1):c.1717G>A (p.Val573Ile) rs188554662
NM_144612.6(LOXHD1):c.1730T>G (p.Leu577Arg) rs727503147
NM_144612.6(LOXHD1):c.1828G>A (p.Glu610Lys) rs535637788
NM_144612.6(LOXHD1):c.1875T>C (p.Asp625=) rs886053836
NM_144612.6(LOXHD1):c.1876G>T (p.Gly626Cys) rs34589386
NM_144612.6(LOXHD1):c.1887C>T (p.Ser629=) rs189550119
NM_144612.6(LOXHD1):c.1944C>T (p.Ser648=) rs369039902
NM_144612.6(LOXHD1):c.197C>G (p.Thr66Arg) rs199536893
NM_144612.6(LOXHD1):c.2027A>G (p.Asp676Gly) rs16978578
NM_144612.6(LOXHD1):c.2100G>A (p.Thr700=) rs367826075
NM_144612.6(LOXHD1):c.2227A>G (p.Thr743Ala) rs759325484
NM_144612.6(LOXHD1):c.2245-13G>A rs749554659
NM_144612.6(LOXHD1):c.231C>T (p.Leu77=) rs200306249
NM_144612.6(LOXHD1):c.2370C>T (p.Asp790=) rs34723936
NM_144612.6(LOXHD1):c.2386G>A (p.Gly796Arg) rs886053835
NM_144612.6(LOXHD1):c.2438-9C>A rs886053834
NM_144612.6(LOXHD1):c.245+5G>A rs374277176
NM_144612.6(LOXHD1):c.246-14C>T rs139812523
NM_144612.6(LOXHD1):c.2468G>C (p.Gly823Ala) rs886053833
NM_144612.6(LOXHD1):c.2497C>T (p.Arg833Ter) rs188119157
NM_144612.6(LOXHD1):c.2516A>T (p.Tyr839Phe) rs752014328
NM_144612.6(LOXHD1):c.2575C>T (p.Arg859Trp) rs372546084
NM_144612.6(LOXHD1):c.2648C>T (p.Thr883Met) rs186315227
NM_144612.6(LOXHD1):c.274G>A (p.Val92Ile) rs115275492
NM_144612.6(LOXHD1):c.2770C>T (p.Arg924Trp) rs886053832
NM_144612.6(LOXHD1):c.2839G>A (p.Asp947Asn) rs371808826
NM_144612.6(LOXHD1):c.2851G>A (p.Glu951Lys) rs138190875
NM_144612.6(LOXHD1):c.287G>A (p.Arg96Gln) rs376467400
NM_144612.6(LOXHD1):c.2907G>A (p.Glu969=) rs886053831
NM_144612.6(LOXHD1):c.3016G>A (p.Glu1006Lys) rs868583953
NM_144612.6(LOXHD1):c.3024C>T (p.Val1008=) rs370616818
NM_144612.6(LOXHD1):c.3090G>A (p.Thr1030=) rs113994614
NM_144612.6(LOXHD1):c.3165C>T (p.Gly1055=) rs768431469
NM_144612.6(LOXHD1):c.3195C>T (p.Ser1065=) rs886053830
NM_144612.6(LOXHD1):c.3236A>G (p.Tyr1079Cys) rs367863703
NM_144612.6(LOXHD1):c.3269G>A (p.Arg1090Gln) rs118174674
NM_144612.6(LOXHD1):c.329T>C (p.Ile110Thr) rs556403714
NM_144612.6(LOXHD1):c.3371G>A (p.Arg1124His) rs762111513
NM_144612.6(LOXHD1):c.3426G>A (p.Val1142=) rs200068167
NM_144612.6(LOXHD1):c.3597C>G (p.Leu1199=) rs886053829
NM_144612.6(LOXHD1):c.3648A>G (p.Thr1216=) rs886053828
NM_144612.6(LOXHD1):c.3673A>G (p.Ser1225Gly) rs370149278
NM_144612.6(LOXHD1):c.3847G>A (p.Glu1283Lys) rs373541883
NM_144612.6(LOXHD1):c.3924C>T (p.Tyr1308=) rs184966970
NM_144612.6(LOXHD1):c.3941C>T (p.Thr1314Ile) rs182125538
NM_144612.6(LOXHD1):c.3951C>A (p.Val1317=) rs779507390
NM_144612.6(LOXHD1):c.4068G>A (p.Arg1356=) rs539688337
NM_144612.6(LOXHD1):c.409C>T (p.Arg137Cys) rs369244277
NM_144612.6(LOXHD1):c.4148C>T (p.Thr1383Met) rs7244681
NM_144612.6(LOXHD1):c.4180G>A (p.Val1394Met) rs368216643
NM_144612.6(LOXHD1):c.4239C>T (p.Cys1413=) rs886053827
NM_144612.6(LOXHD1):c.4376-6G>A rs369463541
NM_144612.6(LOXHD1):c.4428G>A (p.Thr1476=) rs577112286
NM_144612.6(LOXHD1):c.4476_4477insT (p.Glu1493Ter) rs763478051
NM_144612.6(LOXHD1):c.4523G>A (p.Arg1508Lys) rs199518750
NM_144612.6(LOXHD1):c.457C>T (p.Arg153Cys) rs112618498
NM_144612.6(LOXHD1):c.4690C>T (p.Leu1564Phe) rs573600473
NM_144612.6(LOXHD1):c.4743G>A (p.Glu1581=) rs886053826
NM_144612.6(LOXHD1):c.4824C>G (p.Val1608=) rs114557260
NM_144612.6(LOXHD1):c.4868A>G (p.Glu1623Gly) rs12606417
NM_144612.6(LOXHD1):c.4978A>G (p.Lys1660Glu) rs868705338
NM_144612.6(LOXHD1):c.5047G>A (p.Val1683Ile) rs571616553
NM_144612.6(LOXHD1):c.5085+1G>A rs1418245706
NM_144612.6(LOXHD1):c.5201A>G (p.Lys1734Arg) rs370816148
NM_144612.6(LOXHD1):c.5204A>G (p.Lys1735Arg) rs368286192
NM_144612.6(LOXHD1):c.5214-3C>T rs528236655
NM_144612.6(LOXHD1):c.5312C>G (p.Pro1771Arg) rs772058659
NM_144612.6(LOXHD1):c.5506+12G>A rs200518261
NM_144612.6(LOXHD1):c.5585C>T (p.Ser1862Leu) rs886053825
NM_144612.6(LOXHD1):c.572A>G (p.Asp191Gly) rs886053842
NM_144612.6(LOXHD1):c.5743C>T (p.Arg1915Cys) rs886053824
NM_144612.6(LOXHD1):c.5799C>T (p.Asp1933=) rs559560065
NM_144612.6(LOXHD1):c.580A>T (p.Ile194Phe) rs886053841
NM_144612.6(LOXHD1):c.5864-14C>T rs886053823
NM_144612.6(LOXHD1):c.5T>C (p.Met2Thr) rs761525328
NM_144612.6(LOXHD1):c.6057T>C (p.Cys2019=) rs199645176
NM_144612.6(LOXHD1):c.6066C>T (p.His2022=) rs753440039
NM_144612.6(LOXHD1):c.611-15T>C rs146912450
NM_144612.6(LOXHD1):c.611-8G>A rs748870133
NM_144612.6(LOXHD1):c.6147C>T (p.Tyr2049=) rs374858340
NM_144612.6(LOXHD1):c.6274G>A (p.Val2092Ile) rs182149228
NM_144612.6(LOXHD1):c.6413G>A (p.Arg2138Gln) rs148468627
NM_144612.6(LOXHD1):c.6473G>A (p.Arg2158His) rs886053822
NM_144612.6(LOXHD1):c.6555C>T (p.Ala2185=) rs189873733
NM_144612.6(LOXHD1):c.821C>T (p.Ala274Val) rs886053840
NM_144612.6(LOXHD1):c.868G>A (p.Gly290Arg) rs564030670
NM_144612.6(LOXHD1):c.889A>C (p.Thr297Pro) rs117747744

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