List of variants in gene TSKU reported as likely benign

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_015516.4(TSKU):c.484G>T (p.Val162Leu)	rs148661218	0.00181
NM_015516.4(TSKU):c.730G>C (p.Glu244Gln)	rs768003667	0.00007
NM_015516.4(TSKU):c.1026C>T (p.Thr342=)	rs543814340	0.00002
NM_015516.4(TSKU):c.206G>A (p.Arg69Gln)
NM_015516.4(TSKU):c.944G>A (p.Arg315Gln)

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