ClinVar Miner

List of variants in gene NALCN reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_052867.4(NALCN):c.208G>T (p.Val70Leu) rs75606652 0.00116
NM_052867.4(NALCN):c.4103+4G>C rs201402954 0.00078
NM_052867.4(NALCN):c.1115G>A (p.Arg372His) rs75772824 0.00066
NM_052867.4(NALCN):c.1567A>G (p.Ile523Val) rs150580612 0.00060
NM_052867.4(NALCN):c.2193-9T>G rs367983664 0.00046
NM_052867.4(NALCN):c.4209G>A (p.Pro1403=) rs143988868 0.00040
NM_052867.4(NALCN):c.3057+8A>T rs371743357 0.00034
NM_052867.4(NALCN):c.2457-4C>G rs200652639 0.00025
NM_052867.4(NALCN):c.693A>G (p.Pro231=) rs151026600 0.00025
NM_052867.4(NALCN):c.4581C>T (p.Asp1527=) rs143067409 0.00016
NM_052867.4(NALCN):c.1280T>C (p.Val427Ala) rs371662809 0.00011
NM_052867.4(NALCN):c.175A>G (p.Met59Val) rs77203309 0.00009
NM_052867.4(NALCN):c.2580-7C>T rs368616205 0.00008
NM_052867.4(NALCN):c.942+8G>A rs374004710 0.00006
NM_052867.4(NALCN):c.522G>A (p.Ser174=) rs201866988 0.00004
NM_052867.4(NALCN):c.2495A>G (p.Tyr832Cys) rs549182297 0.00003
NM_052867.4(NALCN):c.3495G>A (p.Thr1165=) rs757748955 0.00001
NM_052867.4(NALCN):c.1014G>A (p.Ser338=)
NM_052867.4(NALCN):c.1026T>C (p.Thr342=)
NM_052867.4(NALCN):c.1425G>A (p.Thr475=)
NM_052867.4(NALCN):c.1434+5T>C
NM_052867.4(NALCN):c.2364+6_2364+12del
NM_052867.4(NALCN):c.3036C>T (p.Ser1012=)
NM_052867.4(NALCN):c.318C>T (p.Arg106=)
NM_052867.4(NALCN):c.3354G>A (p.Val1118=) rs756595210
NM_052867.4(NALCN):c.3852C>A (p.Gly1284=) rs772803115
NM_052867.4(NALCN):c.4455C>T (p.Ile1485=)
NM_052867.4(NALCN):c.4578C>T (p.Gly1526=)
NM_052867.4(NALCN):c.4977C>G (p.Asp1659Glu) rs78817184
NM_052867.4(NALCN):c.4977C>T (p.Asp1659=) rs78817184
NM_052867.4(NALCN):c.5024-10_5024-7dup rs569363992
NM_052867.4(NALCN):c.5127G>A (p.Ala1709=) rs111638537
NM_052867.4(NALCN):c.663T>C (p.Ser221=)

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