ClinVar Miner

List of variants in gene DHODH reported as uncertain significance for Miller syndrome

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Total variants: 49
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HGVS dbSNP
NM_001361.5(DHODH):c.*1035_*1038del rs886052283
NM_001361.5(DHODH):c.*144G>A
NM_001361.5(DHODH):c.*189C>T rs750442401
NM_001361.5(DHODH):c.*216G>A
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.*500G>A rs886052281
NM_001361.5(DHODH):c.*645T>C
NM_001361.5(DHODH):c.*64C>G rs886052280
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.*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.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.22-11C>T rs770515591
NM_001361.5(DHODH):c.454G>A (p.Gly152Arg) rs267606766
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.570C>T (p.Ala190=) rs149123373
NM_001361.5(DHODH):c.606C>T (p.Gly202=)
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.73G>A (p.Ala25Thr)
NM_001361.5(DHODH):c.753C>A (p.Val251=) rs373893426
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.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

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