ClinVar Miner

List of variants reported as likely pathogenic for Sialic acid storage disease, severe infantile type

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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_012434.5(SLC17A5):c.116G>A (p.Arg39His) rs769235753 0.00001
NM_012434.5(SLC17A5):c.1001C>G (p.Pro334Arg) rs119491110
NM_012434.5(SLC17A5):c.1111G>A (p.Gly371Arg) rs1277966688
NM_012434.5(SLC17A5):c.409del (p.Met137fs) rs794729653
NM_012434.5(SLC17A5):c.467_525+125del
NM_012434.5(SLC17A5):c.527G>T (p.Gly176Val)
NM_012434.5(SLC17A5):c.744_747del (p.Ser249fs) rs753141230

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