ClinVar Miner

List of variants in gene SGCD reported as likely benign for not specified

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Gene type:
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Total variants: 37
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HGVS dbSNP
NM_000337.5(SGCD):c.*2A>C rs200757725
NM_000337.5(SGCD):c.*4A>G rs144825977
NM_000337.5(SGCD):c.-13G>T rs1440354794
NM_000337.5(SGCD):c.-30G>A rs374043017
NM_000337.5(SGCD):c.-44+11G>A rs184722381
NM_000337.5(SGCD):c.-44+11_-44+13delGTT rs1554093300
NM_000337.5(SGCD):c.-80G>T rs1057522676
NM_000337.5(SGCD):c.105G>C (p.Leu35=) rs193922392
NM_000337.5(SGCD):c.123C>G (p.Leu41=) rs200670993
NM_000337.5(SGCD):c.144G>C (p.Val48=) rs372152495
NM_000337.5(SGCD):c.15G>C (p.Glu5Asp) rs549319429
NM_000337.5(SGCD):c.177C>T (p.Val59=) rs727505265
NM_000337.5(SGCD):c.193-12G>T rs727503421
NM_000337.5(SGCD):c.193-17T>G rs201079829
NM_000337.5(SGCD):c.213G>A (p.Arg71=) rs74846539
NM_000337.5(SGCD):c.290G>A (p.Arg97Gln) rs45559835
NM_000337.5(SGCD):c.294+15A>C rs377470284
NM_000337.5(SGCD):c.294+8T>C rs11748588
NM_000337.5(SGCD):c.295-20C>A rs144250417
NM_000337.5(SGCD):c.3+11C>T rs374790317
NM_000337.5(SGCD):c.3+14G>A rs538229806
NM_000337.5(SGCD):c.3+19C>T rs182715924
NM_000337.5(SGCD):c.383-11A>T rs727504584
NM_000337.5(SGCD):c.383-17_383-10delCTCTCTAT rs727504998
NM_000337.5(SGCD):c.393C>T (p.Ala131=) rs397517922
NM_000337.5(SGCD):c.394G>A (p.Val132Ile) rs367819390
NM_000337.5(SGCD):c.45T>A (p.Pro15=) rs727505092
NM_000337.5(SGCD):c.543T>G (p.Pro181=) rs200451694
NM_000337.5(SGCD):c.576-14_576-10delTGGGT rs1064794366
NM_000337.5(SGCD):c.576-15T>C rs918017706
NM_000337.5(SGCD):c.594G>T (p.Arg198=) rs754875886
NM_000337.5(SGCD):c.699+18C>G rs180898690
NM_000337.5(SGCD):c.69C>T (p.Tyr23=) rs397517923
NM_000337.5(SGCD):c.717G>A (p.Ala239=) rs145430692
NM_000337.5(SGCD):c.786G>A (p.Glu262=) rs1197695649
NM_000337.5(SGCD):c.817C>T (p.Leu273=) rs375029639
NM_000337.5(SGCD):c.848A>G (p.Gln283Arg) rs397516338

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