ClinVar Miner

List of variants in gene SLC37A4 reported as likely benign for not provided

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Gene type:
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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001164277.2(SLC37A4):c.148+332T>C rs71482166 0.01809
NM_001164277.2(SLC37A4):c.871+56G>A rs117813240 0.01228
NM_001164277.2(SLC37A4):c.986-91C>G rs74536648 0.01050
NM_001164277.2(SLC37A4):c.1275C>T (p.Ser425=) rs35010541 0.01045
NM_001164277.2(SLC37A4):c.149-264G>A rs77425559 0.01038
NM_001164277.2(SLC37A4):c.986-92T>C rs75212035 0.00798
NM_001164277.2(SLC37A4):c.1062C>T (p.Asn354=) rs61730035 0.00758
NM_001164277.2(SLC37A4):c.149-265C>T rs148686645 0.00592
NM_001164277.2(SLC37A4):c.872-123G>C rs59206251 0.00546
NM_001164277.2(SLC37A4):c.872-21T>C rs116083740 0.00282
NM_001164277.2(SLC37A4):c.593A>T (p.Asn198Ile) rs34203644 0.00280
NM_001164277.2(SLC37A4):c.467C>T (p.Ala156Val) rs201036248 0.00214
NM_001164277.2(SLC37A4):c.1240C>T (p.Leu414=) rs200703321 0.00041
NM_001164277.2(SLC37A4):c.1128C>T (p.Gly376=) rs200713586 0.00013
NM_001164277.2(SLC37A4):c.150G>T (p.Gly50=) rs202137454 0.00010
NM_001164277.2(SLC37A4):c.-699-7C>G rs570606800 0.00001
NM_001164277.2(SLC37A4):c.498C>T (p.Arg166=) rs1592113035
NM_001164277.2(SLC37A4):c.603C>T (p.Pro201=) rs368398459
NM_001164277.2(SLC37A4):c.872C>T (p.Ala291Val) rs200147602

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