ClinVar Miner

List of variants in gene CTNS reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_004937.3(CTNS):c.*1031_*1033dup rs1355863772 0.18984
NM_004937.3(CTNS):c.124G>A (p.Val42Ile) rs35086888 0.01867
NM_004937.3(CTNS):c.*1669C>T rs117079843 0.01548
NM_004937.3(CTNS):c.*2012C>T rs138871128 0.00686
NM_004937.3(CTNS):c.108C>T (p.Asn36=) rs117404824 0.00664
NM_004937.3(CTNS):c.*2132G>A rs74485511 0.00447
NM_004937.3(CTNS):c.*2119G>T rs80249487 0.00388
NM_004937.3(CTNS):c.462-7C>A rs189632527 0.00259
NM_004937.3(CTNS):c.*180C>T rs552754402 0.00003
NM_004937.3(CTNS):c.*1174CT[1] rs397857879
NM_004937.3(CTNS):c.*847C>T rs146131305

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