ClinVar Miner

List of variants in gene DLAT reported as uncertain significance for X-linked syndromic intellectual disability

Included ClinVar conditions (165):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_001931.4(DLAT):c.-137G>A rs886047692
NM_001931.4(DLAT):c.-203C>T rs781987834
NM_001931.4(DLAT):c.-212C>G rs587656558
NM_001931.4(DLAT):c.-222C>T rs587750751
NM_001931.4(DLAT):c.-338T>C rs587698124
NM_001931.4(DLAT):c.-383T>A rs886047691
NM_001931.4(DLAT):c.-471C>T rs886047690
NM_001931.4(DLAT):c.-500C>T rs886047689
NM_001931.4(DLAT):c.-572G>A rs183456915
NM_001931.4(DLAT):c.-590G>A rs587721916
NM_001931.4(DLAT):c.-647C>A rs190887558
NM_001931.4(DLAT):c.-90G>C rs587665696
NM_001931.4(DLAT):c.1142A>G (p.Asp381Gly) rs144235197
NM_001931.4(DLAT):c.1202C>T (p.Pro401Leu) rs781794850
NM_001931.4(DLAT):c.1290+5G>A rs886047694
NM_001931.4(DLAT):c.1399-13C>T rs374698306
NM_001931.4(DLAT):c.210G>C (p.Arg70=) rs782739576
NM_001931.4(DLAT):c.318C>A (p.Gly106=) rs201070254
NM_001931.4(DLAT):c.355A>G (p.Ile119Val) rs1555179245
NM_001931.4(DLAT):c.396dup (p.Ala133Serfs) rs782173047
NM_001931.4(DLAT):c.402T>C (p.Thr134=) rs886047693
NM_001931.4(DLAT):c.412G>T (p.Glu138Ter) rs781991355
NM_001931.4(DLAT):c.506+11C>T rs77846695
NM_001931.4(DLAT):c.506+12G>A rs372355218
NM_001931.4(DLAT):c.55G>C (p.Glu19Gln) rs61757217
NM_001931.4(DLAT):c.572C>T (p.Ala191Val) rs200500508
NM_001931.4(DLAT):c.606G>A (p.Ser202=) rs148153443
NM_001931.4(DLAT):c.828G>T (p.Leu276=) rs199835215
NM_001931.4(DLAT):c.946C>T (p.Pro316Ser) rs149088081
NM_001931.4(DLAT):c.974C>T (p.Pro325Leu) rs782527135
NM_001931.4(DLAT):c.991C>G (p.Pro331Ala) rs78320677

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