List of variants in gene CASK reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001367721.1(CASK):c.2734C>T (p.Leu912Phe)	rs777220099	0.00002
NM_001367721.1(CASK):c.1394C>G (p.Ser465Cys)	rs2147201432
NM_001367721.1(CASK):c.1447G>C (p.Glu483Gln)
NM_001367721.1(CASK):c.1727C>T (p.Ser576Leu)	rs2065202221
NM_001367721.1(CASK):c.2324C>G (p.Thr775Ser)	rs2519688829
NM_001367721.1(CASK):c.2482G>A (p.Glu828Lys)	rs192044507
NM_001367721.1(CASK):c.881_882delinsCC (p.Gln294Pro)	rs2519079470

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