ClinVar Miner

List of variants in gene combination CLCNKA, LOC106501712 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004070.4(CLCNKA):c.1612C>T (p.Arg538Cys)	rs139564196	0.00350
NM_004070.4(CLCNKA):c.969-7C>G	rs201309731	0.00227
NM_004070.4(CLCNKA):c.1708del (p.Val570fs)	rs556704888
NM_004070.4(CLCNKA):c.679A>G (p.Met227Val)

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