ClinVar Miner

List of variants in gene SGCD reported as uncertain significance by Invitae

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Total variants: 38
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HGVS dbSNP
NM_000337.5(SGCD):c.101G>A (p.Cys34Tyr)
NM_000337.5(SGCD):c.160A>G (p.Ile54Val) rs200671745
NM_000337.5(SGCD):c.175G>T (p.Val59Phe) rs1274415049
NM_000337.5(SGCD):c.191T>C (p.Ile64Thr) rs376780156
NM_000337.5(SGCD):c.194A>G (p.Asp65Gly)
NM_000337.5(SGCD):c.197G>C (p.Gly66Ala)
NM_000337.5(SGCD):c.19T>C (p.Tyr7His) rs1561633494
NM_000337.5(SGCD):c.1A>G (p.Met1Val) rs756367674
NM_000337.5(SGCD):c.285G>C (p.Gln95His) rs1421460814
NM_000337.5(SGCD):c.340A>G (p.Ile114Val)
NM_000337.5(SGCD):c.354G>T (p.Gln118His) rs770930747
NM_000337.5(SGCD):c.359A>C (p.Lys120Thr) rs1385323214
NM_000337.5(SGCD):c.394G>A (p.Val132Ile) rs367819390
NM_000337.5(SGCD):c.434C>G (p.Ser145Cys) rs1324593212
NM_000337.5(SGCD):c.437G>T (p.Gly146Val) rs1438925313
NM_000337.5(SGCD):c.451T>G (p.Ser151Ala) rs121909298
NM_000337.5(SGCD):c.458A>G (p.Asp153Gly) rs752000538
NM_000337.5(SGCD):c.461A>G (p.Asn154Ser) rs759767804
NM_000337.5(SGCD):c.494G>A (p.Arg165Gln) rs727503423
NM_000337.5(SGCD):c.547G>A (p.Val183Ile)
NM_000337.5(SGCD):c.559C>T (p.Pro187Ser) rs769250018
NM_000337.5(SGCD):c.566A>G (p.Lys189Arg) rs538002169
NM_000337.5(SGCD):c.593G>A (p.Arg198Gln)
NM_000337.5(SGCD):c.659C>T (p.Thr220Ile) rs1471128348
NM_000337.5(SGCD):c.662G>A (p.Cys221Tyr) rs1561899959
NM_000337.5(SGCD):c.699+8delA
NM_000337.5(SGCD):c.744T>G (p.His248Gln) rs1160680799
NM_000337.5(SGCD):c.755C>T (p.Thr252Met) rs199520526
NM_000337.5(SGCD):c.761C>T (p.Thr254Ile) rs372607729
NM_000337.5(SGCD):c.767C>T (p.Thr256Met) rs578056399
NM_000337.5(SGCD):c.793G>A (p.Val265Ile) rs772185467
NM_000337.5(SGCD):c.799G>A (p.Ala267Thr)
NM_000337.5(SGCD):c.821C>T (p.Ser274Phe)
NM_000337.5(SGCD):c.832G>A (p.Ala278Thr) rs753240054
NM_000337.5(SGCD):c.832G>T (p.Ala278Ser)
NM_000337.5(SGCD):c.91C>T (p.Arg31Trp)
NM_000337.5(SGCD):c.92G>A (p.Arg31Gln) rs200476861
NM_000337.5(SGCD):c.98G>A (p.Arg33Gln) rs1488623227

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