List of variants in gene CNNM2 reported as benign for inherited renal tubular disease

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_017649.5(CNNM2):c.2418+20T>C	rs943036	0.40434
NM_017649.5(CNNM2):c.1842T>C (p.Ser614=)	rs2275271	0.40382
NM_017649.5(CNNM2):c.*879G>A	rs1046411	0.32109
NM_017649.5(CNNM2):c.*3C>T	rs2296568	0.10834
NM_017649.5(CNNM2):c.2310C>T (p.Ala770=)	rs943037	0.08142
NM_017649.5(CNNM2):c.2544C>T (p.Asp848=)	rs35647154	0.05419
NM_017649.5(CNNM2):c.113G>A (p.Arg38Gln)	rs76057237	0.05045
NM_017649.5(CNNM2):c.1622-6C>T	rs74464353	0.01345
NM_017649.5(CNNM2):c.*794G>A	rs41287480	0.01310
NM_017649.5(CNNM2):c.*904G>C	rs145537350	0.00916
NM_017649.5(CNNM2):c.*619A>G	rs138807273	0.00554
NM_017649.5(CNNM2):c.564C>T (p.Ser188=)	rs117691462	0.00404
NM_017649.5(CNNM2):c.*891G>T	rs185818969	0.00291
NM_017649.5(CNNM2):c.*52C>T	rs367767821	0.00271
NM_017649.5(CNNM2):c.*528G>A	rs3740388	0.00255
NM_017649.5(CNNM2):c.1134C>T (p.Leu378=)	rs2297785	0.00253
NM_017649.5(CNNM2):c.2073+14T>C	rs184406418	0.00150
NM_017649.5(CNNM2):c.903C>T (p.Tyr301=)	rs140279763	0.00044
NM_017649.5(CNNM2):c.604G>A (p.Ala202Thr)	rs75800852	0.00034
NM_017649.5(CNNM2):c.342G>T (p.Thr114=)	rs375416482	0.00029
NM_017649.5(CNNM2):c.1515C>T (p.Pro505=)	rs144140948	0.00026
NM_017649.5(CNNM2):c.*311G>A	rs376027544	0.00023
NM_017649.5(CNNM2):c.*543A>G	rs145025818	0.00018
NM_017649.5(CNNM2):c.*34C>T	rs202217837	0.00015
NM_017649.5(CNNM2):c.*1162G>A	rs148051463	0.00014
NM_017649.5(CNNM2):c.*455C>T	rs3740389	0.00006
NM_017649.5(CNNM2):c.801C>T (p.Cys267=)	rs367789750	0.00004
NM_017649.5(CNNM2):c.90C>T (p.Arg30=)	rs202027427	0.00004
NM_017649.5(CNNM2):c.*1246G>C	rs553490290	0.00001
NM_017649.5(CNNM2):c.1128C>T (p.Ile376=)	rs770748859	0.00001
NM_017649.5(CNNM2):c.-110A>T	rs555951352
NM_017649.5(CNNM2):c.1094C>T (p.Ser365Phe)	rs1845549123

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