ClinVar Miner

List of variants in gene SLC37A4 reported as uncertain significance by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 12
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HGVS dbSNP
NM_001164277.1(SLC37A4):c.1099G>A (p.Ala367Thr) rs80356492
NM_001164277.1(SLC37A4):c.1168C>T (p.His390Tyr) rs199764888
NM_001164277.1(SLC37A4):c.1240C>T (p.Leu414=) rs200703321
NM_001164277.1(SLC37A4):c.1252C>T (p.Arg418Cys)
NM_001164277.1(SLC37A4):c.149G>A (p.Gly50Glu) rs193302877
NM_001164277.1(SLC37A4):c.492C>A (p.Ser164Arg) rs369399624
NM_001164277.1(SLC37A4):c.497G>A (p.Arg166His) rs186476316
NM_001164277.1(SLC37A4):c.556C>T (p.Leu186Phe)
NM_001164277.1(SLC37A4):c.785-7A>G rs781887799
NM_001164277.1(SLC37A4):c.839C>T (p.Ala280Val) rs555640045
NM_001164277.1(SLC37A4):c.878T>C (p.Leu293Pro) rs886042302
NM_001164277.1(SLC37A4):c.930C>T (p.Gly310=)

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