ClinVar Miner

List of variants in gene SGCD reported as uncertain significance for not specified

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Total variants: 14
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HGVS dbSNP
NM_000337.5(SGCD):c.160A>G (p.Ile54Val) rs200671745
NM_000337.5(SGCD):c.193-12G>T rs727503421
NM_000337.5(SGCD):c.383-11A>T rs727504584
NM_000337.5(SGCD):c.383-17_383-10dup8 rs727504998
NM_000337.5(SGCD):c.4-12C>T rs727504580
NM_000337.5(SGCD):c.451T>G (p.Ser151Ala) rs121909298
NM_000337.5(SGCD):c.494G>A (p.Arg165Gln) rs727503423
NM_000337.5(SGCD):c.506C>T (p.Ala169Val) rs876658001
NM_000337.5(SGCD):c.697G>A (p.Glu233Lys) rs768979513
NM_000337.5(SGCD):c.699+18C>G rs180898690
NM_000337.5(SGCD):c.699+72A>C rs376317697
NM_000337.5(SGCD):c.731C>T (p.Pro244Leu) rs375159661
NM_000337.5(SGCD):c.839C>A (p.Ser280Tyr) rs397516337
NM_000337.5(SGCD):c.92G>A (p.Arg31Gln) rs200476861

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