ClinVar Miner

List of variants in gene DHODH studied for bone disorder

Included ClinVar conditions (1350):
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Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_001361.5(DHODH):c.435-38G>C rs11075914 0.99994
NM_001361.5(DHODH):c.*1051A>G rs2287999 0.55850
NM_001361.5(DHODH):c.*783A>G rs2288000 0.55819
NM_001361.5(DHODH):c.*1171T>C rs2287998 0.55799
NM_001361.5(DHODH):c.*574G>T rs2288001 0.55770
NM_001361.5(DHODH):c.518-39G>T rs1862752 0.54545
NM_001361.5(DHODH):c.19A>C (p.Lys7Gln) rs3213422 0.54012
NM_001361.5(DHODH):c.*569G>A rs113365769 0.10579
NM_001361.4(DHODH):c.-29A>G rs34270657 0.06520
NM_001361.5(DHODH):c.*595C>T rs111810095 0.04483
NM_001361.5(DHODH):c.*612T>C rs7191724 0.04342
NM_001361.5(DHODH):c.819+10G>A rs114267707 0.01597
NM_001361.5(DHODH):c.*1014C>T rs79926352 0.01533
NM_001361.5(DHODH):c.*748C>T rs117655998 0.01294
NM_001361.5(DHODH):c.573G>A (p.Ala191=) rs148523165 0.00894
NM_001361.5(DHODH):c.*868A>G rs149599098 0.00547
NM_001361.5(DHODH):c.457C>A (p.Leu153Ile) rs61741731 0.00410
NM_001361.5(DHODH):c.294C>T (p.Asp98=) rs61747639 0.00227
NM_001361.5(DHODH):c.72C>T (p.Phe24=) rs61753576 0.00163
NM_001361.5(DHODH):c.765C>T (p.Ile255=) rs61757214 0.00128
NM_001361.5(DHODH):c.949C>T (p.Arg317Trp) rs192923495 0.00088
NM_001361.5(DHODH):c.*1088T>C rs567852382 0.00063
NM_001361.5(DHODH):c.403C>T (p.Arg135Cys) rs201230446 0.00054
NM_001361.5(DHODH):c.*936T>C rs763009216 0.00053
NM_001361.5(DHODH):c.682G>A (p.Glu228Lys) rs201202896 0.00051
NM_001361.5(DHODH):c.804C>T (p.Ala268=) rs374538940 0.00048
NM_001361.5(DHODH):c.890G>A (p.Arg297His) rs200181357 0.00045
NM_001361.5(DHODH):c.518-11G>A rs201023112 0.00028
NM_001361.5(DHODH):c.753C>A (p.Val251=) rs373893426 0.00021
NM_001361.5(DHODH):c.*980A>G rs766237954 0.00016
NM_001361.5(DHODH):c.570C>T (p.Ala190=) rs149123373 0.00016
NM_001361.5(DHODH):c.*841G>A rs764720601 0.00014
NM_001361.5(DHODH):c.655G>A (p.Gly219Arg) rs369556950 0.00013
NM_001361.5(DHODH):c.881G>A (p.Gly294Asp) rs369181023 0.00013
NM_001361.5(DHODH):c.*819A>G rs886052282 0.00010
NM_001361.5(DHODH):c.606C>T (p.Gly202=) rs573177564 0.00007
NM_001361.5(DHODH):c.*1174T>G rs148338434 0.00006
NM_001361.5(DHODH):c.*795C>T rs1042981090 0.00006
NM_001361.5(DHODH):c.454G>A (p.Gly152Arg) rs267606766 0.00006
NM_001361.5(DHODH):c.154G>C (p.Glu52Gln) rs368395651 0.00005
NM_001361.5(DHODH):c.*645T>C rs1324665374 0.00004
NM_001361.5(DHODH):c.104G>A (p.Arg35His) rs199675109 0.00004
NM_001361.5(DHODH):c.517+8G>A rs758925798 0.00004
NM_001361.5(DHODH):c.605G>A (p.Gly202Asp) rs267606767 0.00004
NM_001361.5(DHODH):c.492G>T (p.Gln164His) rs768224976 0.00003
NM_001361.5(DHODH):c.595C>T (p.Arg199Cys) rs267606769 0.00003
NM_001361.5(DHODH):c.869C>T (p.Ala290Val) rs199626701 0.00003
NM_001361.5(DHODH):c.22-11C>T rs770515591 0.00001
NM_001361.5(DHODH):c.546G>T (p.Gly182=) rs954515669 0.00001
NM_001361.5(DHODH):c.666C>G (p.Ser222Arg) rs528598713 0.00001
NM_001361.5(DHODH):c.681C>T (p.Ala227=) rs776932166 0.00001
NM_001361.5(DHODH):c.730C>T (p.Arg244Trp) rs267606768 0.00001
NM_001361.5(DHODH):c.807T>A (p.Ser269Arg) rs886052277 0.00001
NM_001361.5(DHODH):c.820T>C (p.Leu274=) rs886052278 0.00001
NM_001361.5(DHODH):c.*1035_*1038del rs886052283
NM_001361.5(DHODH):c.*500G>A rs886052281
NM_001361.5(DHODH):c.14A>G (p.His5Arg) rs1430616655
NM_001361.5(DHODH):c.248_261del (p.Leu83fs) rs776973679
NM_001361.5(DHODH):c.262C>T (p.Arg88Ter)
NM_001361.5(DHODH):c.498G>A (p.Lys166=) rs199920621
NM_001361.5(DHODH):c.505A>C (p.Lys169Gln) rs1243279715
NM_001361.5(DHODH):c.56G>A (p.Gly19Glu) rs267606765
NM_001361.5(DHODH):c.605G>C (p.Gly202Ala) rs267606767
NM_001361.5(DHODH):c.611del (p.Leu204fs) rs1215488320
NM_001361.5(DHODH):c.616G>A (p.Asp206Asn)
NM_001361.5(DHODH):c.72C>G (p.Phe24Leu) rs61753576
NM_001361.5(DHODH):c.731G>A (p.Arg244Gln)
NM_001361.5(DHODH):c.73G>A (p.Ala25Thr) rs200549060
NM_001361.5(DHODH):c.952G>T (p.Glu318Ter) rs1288171226
NM_001361.5(DHODH):c.959A>C (p.Tyr320Ser) rs886052279
NM_001361.5(DHODH):c.959A>G (p.Tyr320Cys) rs886052279
NM_001361.5(DHODH):c.95G>T (p.Gly32Val)
NM_001361.5(DHODH):c.973+11C>T rs2041242918

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