ClinVar Miner

List of variants in gene SLC37A4 reported as benign for Glucose-6-phosphate transport defect

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001164277.2(SLC37A4):c.1224G>A (p.Thr408=) rs8192696 0.24878
NM_001164277.2(SLC37A4):c.-195-64C>T rs56258965 0.15980
NM_001164277.2(SLC37A4):c.626+19C>T rs741811 0.11021
NM_001164277.2(SLC37A4):c.183T>C (p.Ala61=) rs34123220 0.04188
NM_001164277.2(SLC37A4):c.1278G>A (p.Lys426=) rs34871377 0.01583
NM_001164277.2(SLC37A4):c.626+14C>T rs56394886 0.01293
NM_001164277.2(SLC37A4):c.149-14A>G rs79849261 0.01232
NM_001164277.2(SLC37A4):c.1275C>T (p.Ser425=) rs35010541 0.01045
NM_001164277.2(SLC37A4):c.1062C>T (p.Asn354=) rs61730035 0.00758
NM_001164277.2(SLC37A4):c.593A>T (p.Asn198Ile) rs34203644 0.00280
NM_001164277.2(SLC37A4):c.968C>T (p.Thr323Ile) rs202209699 0.00273
NM_001164277.2(SLC37A4):c.467C>T (p.Ala156Val) rs201036248 0.00206
NM_001164277.2(SLC37A4):c.497G>A (p.Arg166His) rs186476316 0.00076
NM_001164277.2(SLC37A4):c.991A>G (p.Ile331Val) rs201967384 0.00029
NM_001164277.2(SLC37A4):c.80A>G (p.Asn27Ser) rs782308530 0.00005
NM_001164277.2(SLC37A4):c.781G>A (p.Val261Ile) rs561701030 0.00001
NM_001164277.2(SLC37A4):c.1067G>C (p.Ser356Thr) rs547488738
NM_001164277.2(SLC37A4):c.1125-7dup rs2497010654
NM_001164277.2(SLC37A4):c.527= (p.Cys176=) rs56966114
NM_001164277.2(SLC37A4):c.626+10del rs2497027403
NM_001164277.2(SLC37A4):c.626+16G>A rs74673344

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