ClinVar Miner

List of variants in gene SLC37A4 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_001164277.1(SLC37A4):c.*138C>T rs867580827
NM_001164277.1(SLC37A4):c.*139G>T rs886047747
NM_001164277.1(SLC37A4):c.*283T>C rs886047746
NM_001164277.1(SLC37A4):c.*298C>T rs886047745
NM_001164277.1(SLC37A4):c.*31C>T rs564775174
NM_001164277.1(SLC37A4):c.*360C>G rs886047744
NM_001164277.1(SLC37A4):c.*5A>C rs373050741
NM_001164277.1(SLC37A4):c.-108G>A rs536032716
NM_001164277.1(SLC37A4):c.-195-11G>T rs886047751
NM_001164277.1(SLC37A4):c.-217G>A rs527772065
NM_001164277.1(SLC37A4):c.-279C>T rs886047752
NM_001164277.1(SLC37A4):c.-291delG rs754442670
NM_001164277.1(SLC37A4):c.-384G>A rs886047753
NM_001164277.1(SLC37A4):c.-42G>C rs186567090
NM_001164277.1(SLC37A4):c.-50T>G rs886047750
NM_001164277.1(SLC37A4):c.-573C>G rs550169691
NM_001164277.1(SLC37A4):c.-64C>T rs150026242
NM_001164277.1(SLC37A4):c.-670C>T rs886047754
NM_001164277.1(SLC37A4):c.-700+9C>T rs534659292
NM_001164277.1(SLC37A4):c.1119C>T (p.Ala373=) rs886047749
NM_001164277.1(SLC37A4):c.287G>A (p.Trp96Ter) rs121908976
NM_001164277.1(SLC37A4):c.382-6C>A rs756248657
NM_001164277.1(SLC37A4):c.465G>C (p.Leu155=) rs776272750
NM_001164277.1(SLC37A4):c.492C>T (p.Ser164=) rs369399624
NM_001164277.1(SLC37A4):c.81T>A (p.Asn27Lys) rs193302889

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