ClinVar Miner

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

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Total variants: 51
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HGVS dbSNP
NM_000337.5(SGCD):c.-43-1G>A rs767016855
NM_000337.5(SGCD):c.116T>C (p.Val39Ala) rs794729164
NM_000337.5(SGCD):c.123C>G (p.Leu41=) rs200670993
NM_000337.5(SGCD):c.160A>G (p.Ile54Val) rs200671745
NM_000337.5(SGCD):c.191T>C (p.Ile64Thr) rs376780156
NM_000337.5(SGCD):c.193-7A>G rs747018859
NM_000337.5(SGCD):c.213G>A (p.Arg71=) rs74846539
NM_000337.5(SGCD):c.22A>G (p.Thr8Ala) rs1554094932
NM_000337.5(SGCD):c.242_244del (p.Gly81del) rs794729165
NM_000337.5(SGCD):c.268T>A (p.Tyr90Asn) rs786205286
NM_000337.5(SGCD):c.270C>T (p.Tyr90=) rs749273088
NM_000337.5(SGCD):c.295-10C>T rs1334538970
NM_000337.5(SGCD):c.3+7A>G rs1561622931
NM_000337.5(SGCD):c.306G>A (p.Leu102=) rs1554119164
NM_000337.5(SGCD):c.32G>A (p.Arg11Gln) rs752548592
NM_000337.5(SGCD):c.333A>T (p.Thr111=) rs886042290
NM_000337.5(SGCD):c.352C>A (p.Gln118Lys)
NM_000337.5(SGCD):c.357T>C (p.Thr119=) rs886044132
NM_000337.5(SGCD):c.358A>G (p.Lys120Glu)
NM_000337.5(SGCD):c.383-33CTCTCTAT[4] rs727504998
NM_000337.5(SGCD):c.394G>A (p.Val132Ile) rs367819390
NM_000337.5(SGCD):c.402T>C (p.Ala134=) rs190935424
NM_000337.5(SGCD):c.415T>A (p.Phe139Ile) rs886044160
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.45T>A (p.Pro15=) rs727505092
NM_000337.5(SGCD):c.481G>A (p.Ala161Thr) rs886043902
NM_000337.5(SGCD):c.494G>A (p.Arg165Gln) rs727503423
NM_000337.5(SGCD):c.510G>A (p.Glu170=) rs368838376
NM_000337.5(SGCD):c.516A>G (p.Thr172=) rs753952200
NM_000337.5(SGCD):c.543T>G (p.Pro181=) rs200451694
NM_000337.5(SGCD):c.54G>A (p.Val18=) rs756970013
NM_000337.5(SGCD):c.566A>G (p.Lys189Arg) rs538002169
NM_000337.5(SGCD):c.575+6C>T rs886044432
NM_000337.5(SGCD):c.632A>G (p.Asn211Ser) rs794727901
NM_000337.5(SGCD):c.699+18C>G rs180898690
NM_000337.5(SGCD):c.699+49C>G rs752646426
NM_000337.5(SGCD):c.699+76C>T
NM_000337.5(SGCD):c.699+77G>A rs200686844
NM_000337.5(SGCD):c.69C>T (p.Tyr23=) rs397517923
NM_000337.5(SGCD):c.731C>T (p.Pro244Leu) rs375159661
NM_000337.5(SGCD):c.734G>C (p.Arg245Thr) rs886042870
NM_000337.5(SGCD):c.755C>T (p.Thr252Met) rs199520526
NM_000337.5(SGCD):c.756G>A (p.Thr252=) rs756467431
NM_000337.5(SGCD):c.768G>A (p.Thr256=) rs376141942
NM_000337.5(SGCD):c.792C>T (p.Cys264=)
NM_000337.5(SGCD):c.793G>A (p.Val265Ile) rs772185467
NM_000337.5(SGCD):c.848A>G (p.Gln283Arg) rs397516338
NM_000337.5(SGCD):c.89G>C (p.Trp30Ser) rs121909296
NM_000337.5(SGCD):c.8C>T (p.Pro3Leu) rs1554094928
NM_000337.5(SGCD):c.92G>A (p.Arg31Gln) rs200476861

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