ClinVar Miner

List of variants in gene DLAT reported as likely benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP
NM_001931.4(DLAT):c.381+22delT rs5794771
NM_001931.5(DLAT):c.1035A>G (p.Pro345=) rs140302942
NM_001931.5(DLAT):c.1071T>C (p.Val357=)
NM_001931.5(DLAT):c.1142A>G (p.Asp381Gly) rs144235197
NM_001931.5(DLAT):c.144G>A (p.Val48=) rs367745211
NM_001931.5(DLAT):c.1476C>T (p.Pro492=) rs370501604
NM_001931.5(DLAT):c.318C>A (p.Gly106=) rs201070254
NM_001931.5(DLAT):c.372A>C (p.Leu124=)
NM_001931.5(DLAT):c.54C>A (p.Leu18=)
NM_001931.5(DLAT):c.570A>G (p.Gln190=) rs143107853
NM_001931.5(DLAT):c.628G>A (p.Ala210Thr) rs140678772
NM_001931.5(DLAT):c.675C>T (p.Ala225=) rs782220140
NM_001931.5(DLAT):c.754C>T (p.Leu252=) rs139194443
NM_001931.5(DLAT):c.759A>G (p.Ala253=) rs914123181
NM_001931.5(DLAT):c.946C>T (p.Pro316Ser) rs149088081
NM_001931.5(DLAT):c.969A>C (p.Pro323=) rs587627931
NM_001931.5(DLAT):c.991C>G (p.Pro331Ala) rs78320677

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