ClinVar Miner

List of variants studied for Miller syndrome

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Total variants: 83
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HGVS dbSNP
NM_001361.4(DHODH):c.-29A>G rs34270657
NM_001361.5(DHODH):c.*1014C>T rs79926352
NM_001361.5(DHODH):c.*1035_*1038del rs886052283
NM_001361.5(DHODH):c.*1051A>G rs2287999
NM_001361.5(DHODH):c.*1088T>C rs567852382
NM_001361.5(DHODH):c.*1171T>C rs2287998
NM_001361.5(DHODH):c.*1174T>G rs148338434
NM_001361.5(DHODH):c.*139C>T rs140263128
NM_001361.5(DHODH):c.*144G>A
NM_001361.5(DHODH):c.*14C>T rs370049658
NM_001361.5(DHODH):c.*189C>T rs750442401
NM_001361.5(DHODH):c.*216G>A
NM_001361.5(DHODH):c.*252C>T rs147792232
NM_001361.5(DHODH):c.*341C>T
NM_001361.5(DHODH):c.*349A>C
NM_001361.5(DHODH):c.*372C>T
NM_001361.5(DHODH):c.*383G>A
NM_001361.5(DHODH):c.*404G>A rs150155845
NM_001361.5(DHODH):c.*500G>A rs886052281
NM_001361.5(DHODH):c.*569G>A rs113365769
NM_001361.5(DHODH):c.*574G>T rs2288001
NM_001361.5(DHODH):c.*595C>T rs111810095
NM_001361.5(DHODH):c.*612T>C rs7191724
NM_001361.5(DHODH):c.*645T>C
NM_001361.5(DHODH):c.*64C>G rs886052280
NM_001361.5(DHODH):c.*748C>T rs117655998
NM_001361.5(DHODH):c.*783A>G rs2288000
NM_001361.5(DHODH):c.*795C>T
NM_001361.5(DHODH):c.*819A>G rs886052282
NM_001361.5(DHODH):c.*841G>A rs764720601
NM_001361.5(DHODH):c.*868A>G
NM_001361.5(DHODH):c.*936T>C
NM_001361.5(DHODH):c.*980A>G rs766237954
NM_001361.5(DHODH):c.1009A>T (p.Ser337Cys) rs376142632
NM_001361.5(DHODH):c.1020C>T (p.Asp340=) rs199666119
NM_001361.5(DHODH):c.1022C>T (p.Ala341Val) rs61733129
NM_001361.5(DHODH):c.1036C>T (p.Arg346Trp) rs201947120
NM_001361.5(DHODH):c.1043G>C (p.Gly348Ala)
NM_001361.5(DHODH):c.1048T>G (p.Ser350Ala)
NM_001361.5(DHODH):c.14A>G (p.His5Arg)
NM_001361.5(DHODH):c.154G>C (p.Glu52Gln) rs368395651
NM_001361.5(DHODH):c.19A>C (p.Lys7Gln) rs3213422
NM_001361.5(DHODH):c.22-11C>T rs770515591
NM_001361.5(DHODH):c.294C>T (p.Asp98=) rs61747639
NM_001361.5(DHODH):c.403C>T (p.Arg135Cys) rs201230446
NM_001361.5(DHODH):c.454G>A (p.Gly152Arg) rs267606766
NM_001361.5(DHODH):c.457C>A (p.Leu153Ile) rs61741731
NM_001361.5(DHODH):c.492G>T (p.Gln164His) rs768224976
NM_001361.5(DHODH):c.498G>A (p.Lys166=)
NM_001361.5(DHODH):c.505A>C (p.Lys169Gln)
NM_001361.5(DHODH):c.517+8G>A rs758925798
NM_001361.5(DHODH):c.518-11G>A
NM_001361.5(DHODH):c.546G>T (p.Gly182=)
NM_001361.5(DHODH):c.56G>A (p.Gly19Glu) rs267606765
NM_001361.5(DHODH):c.570C>T (p.Ala190=) rs149123373
NM_001361.5(DHODH):c.573G>A (p.Ala191=) rs148523165
NM_001361.5(DHODH):c.595C>T (p.Arg199Cys) rs267606769
NM_001361.5(DHODH):c.605G>A (p.Gly202Asp) rs267606767
NM_001361.5(DHODH):c.605G>C (p.Gly202Ala) rs267606767
NM_001361.5(DHODH):c.606C>T (p.Gly202=)
NM_001361.5(DHODH):c.611del (p.Leu204fs) rs1215488320
NM_001361.5(DHODH):c.655G>A (p.Gly219Arg) rs369556950
NM_001361.5(DHODH):c.666C>G (p.Ser222Arg) rs528598713
NM_001361.5(DHODH):c.681C>T (p.Ala227=) rs776932166
NM_001361.5(DHODH):c.682G>A (p.Glu228Lys) rs201202896
NM_001361.5(DHODH):c.72C>G (p.Phe24Leu)
NM_001361.5(DHODH):c.72C>T (p.Phe24=) rs61753576
NM_001361.5(DHODH):c.730C>T (p.Arg244Trp) rs267606768
NM_001361.5(DHODH):c.73G>A (p.Ala25Thr)
NM_001361.5(DHODH):c.753C>A (p.Val251=) rs373893426
NM_001361.5(DHODH):c.765C>T (p.Ile255=) rs61757214
NM_001361.5(DHODH):c.804C>T (p.Ala268=) rs374538940
NM_001361.5(DHODH):c.807T>A (p.Ser269Arg) rs886052277
NM_001361.5(DHODH):c.819+10G>A rs114267707
NM_001361.5(DHODH):c.820T>C (p.Leu274=) rs886052278
NM_001361.5(DHODH):c.869C>T (p.Ala290Val) rs199626701
NM_001361.5(DHODH):c.881G>A (p.Gly294Asp) rs369181023
NM_001361.5(DHODH):c.890G>A (p.Arg297His) rs200181357
NM_001361.5(DHODH):c.949C>T (p.Arg317Trp) rs192923495
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.973+11C>T
NM_001361.5(DHODH):c.983C>T (p.Pro328Leu)

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