List of variants in gene NALCN reported by University of Washington Center for Mendelian Genomics, University of Washington

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_052867.4(NALCN):c.1526T>C (p.Leu509Ser)	rs786203987
NM_052867.4(NALCN):c.1534T>G (p.Phe512Val)	rs878853132
NM_052867.4(NALCN):c.1538C>A (p.Thr513Asn)	rs878853131
NM_052867.4(NALCN):c.1733A>C (p.Tyr578Ser)	rs786203988
NM_052867.4(NALCN):c.1768C>T (p.Leu590Phe)	rs786203986
NM_052867.4(NALCN):c.3017T>C (p.Val1006Ala)	rs878853130
NM_052867.4(NALCN):c.3050T>C (p.Ile1017Thr)	rs878853129
NM_052867.4(NALCN):c.3493A>C (p.Thr1165Pro)	rs878853128
NM_052867.4(NALCN):c.3542G>A (p.Arg1181Gln)	rs786201003
NM_052867.4(NALCN):c.4338T>G (p.Ile1446Met)	rs878853127
NM_052867.4(NALCN):c.530A>C (p.Gln177Pro)	rs786203984
NM_052867.4(NALCN):c.682C>T (p.His228Tyr)	rs2045687348
NM_052867.4(NALCN):c.934C>A (p.Leu312Ile)	rs878853134
NM_052867.4(NALCN):c.938T>G (p.Val313Gly)	rs786203985
NM_052867.4(NALCN):c.979G>A (p.Glu327Lys)	rs878853133

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