List of variants in gene MCCC2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_022132.5(MCCC2):c.1574+37C>G	rs138725621	0.01241
NM_022132.5(MCCC2):c.282-7G>A	rs115078899	0.00399
NM_022132.5(MCCC2):c.1373+27A>G	rs116092799	0.00281
NM_022132.5(MCCC2):c.450G>C (p.Val150=)	rs151098534	0.00121
NM_022132.5(MCCC2):c.114C>G (p.Gly38=)	rs750638270	0.00014
NM_022132.5(MCCC2):c.539G>A (p.Arg180Gln)	rs145846295	0.00012
NM_022132.5(MCCC2):c.1488+10G>A	rs190514867	0.00007
NM_022132.5(MCCC2):c.417C>T (p.Thr139=)	rs367635502	0.00006
NM_022132.5(MCCC2):c.1674C>T (p.Phe558=)	rs768354167	0.00004
NM_022132.5(MCCC2):c.*6A>G	rs1249235767	0.00001
NM_022132.5(MCCC2):c.1073-9T>C
NM_022132.5(MCCC2):c.1131T>C (p.Phe377=)
NM_022132.5(MCCC2):c.1200C>T (p.Phe400=)
NM_022132.5(MCCC2):c.1332C>T (p.Ser444=)

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