ClinVar Miner

List of variants in gene TALDO1 reported as uncertain significance for carbohydrate metabolism disease

Included ClinVar conditions (161):
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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_006755.1(TALDO1):c.-21_-19dupCGC rs71464113
NM_006755.1(TALDO1):c.-30C>T rs373293125
NM_006755.1(TALDO1):c.-37T>C rs886048655
NM_006755.2(TALDO1):c.*12G>A rs369845141
NM_006755.2(TALDO1):c.*30C>T rs200971004
NM_006755.2(TALDO1):c.*33C>T rs375388046
NM_006755.2(TALDO1):c.-6C>T
NM_006755.2(TALDO1):c.181C>G (p.Leu61Val) rs149640294
NM_006755.2(TALDO1):c.197T>C (p.Ile66Thr) rs146282855
NM_006755.2(TALDO1):c.293A>T (p.Lys98Met) rs758756190
NM_006755.2(TALDO1):c.330-10_330delinsAGA
NM_006755.2(TALDO1):c.356T>C (p.Val119Ala)
NM_006755.2(TALDO1):c.36G>A (p.Glu12=) rs150420496
NM_006755.2(TALDO1):c.402C>T (p.Ile134=) rs886048663
NM_006755.2(TALDO1):c.461+14C>T rs373077928
NM_006755.2(TALDO1):c.462-4G>A
NM_006755.2(TALDO1):c.475C>G (p.Gln159Glu) rs144914498
NM_006755.2(TALDO1):c.476A>G (p.Gln159Arg) rs147961544
NM_006755.2(TALDO1):c.480C>T (p.His160=)
NM_006755.2(TALDO1):c.488A>G (p.His163Arg) rs886048664
NM_006755.2(TALDO1):c.48C>T (p.Asp16=) rs886048658
NM_006755.2(TALDO1):c.574C>T (p.Arg192Cys) rs751425603
NM_006755.2(TALDO1):c.575G>A (p.Arg192His) rs151052416
NM_006755.2(TALDO1):c.604G>A (p.Asp202Asn) rs140985565
NM_006755.2(TALDO1):c.662A>G (p.Tyr221Cys) rs765872752
NM_006755.2(TALDO1):c.68C>G (p.Thr23Ser) rs144787855
NM_006755.2(TALDO1):c.706G>A (p.Ala236Thr)
NM_006755.2(TALDO1):c.726C>T (p.Gly242=) rs764708645
NM_006755.2(TALDO1):c.784G>C (p.Glu262Gln)
NM_006755.2(TALDO1):c.78C>G (p.Ala26=) rs886048659
NM_006755.2(TALDO1):c.884G>A (p.Arg295His)
NM_006755.2(TALDO1):c.888G>A (p.Trp296Ter)
NM_006755.2(TALDO1):c.930C>T (p.Asp310=) rs181385165
NM_006755.2(TALDO1):c.952G>A (p.Asp318Asn) rs866261597
NM_006755.2(TALDO1):c.956C>T (p.Ala319Val)
NM_006755.2(TALDO1):c.971G>A (p.Arg324Gln) rs186015859
NM_006755.2(TALDO1):c.982-8_982-5del rs773135701
NM_006755.2(TALDO1):c.982G>A (p.Glu328Lys)

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