List of variants in gene MCCC1 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_020166.5(MCCC1):c.1337C>T (p.Ala446Val)	rs144182725	0.00068
NM_020166.5(MCCC1):c.1731+6C>A	rs369754994	0.00061
NM_020166.5(MCCC1):c.2009C>T (p.Ala670Val)	rs138937107	0.00049
NM_020166.5(MCCC1):c.2034C>T (p.Ile678=)	rs150305281	0.00037
NM_020166.5(MCCC1):c.384A>C (p.Gly128=)	rs139091481	0.00006
NM_020166.5(MCCC1):c.1701G>A (p.Thr567=)	rs377320336	0.00004
NM_020166.5(MCCC1):c.491+35G>A	rs756188495	0.00003
NM_020166.5(MCCC1):c.491+36A>G	rs376539910	0.00003
NM_020166.5(MCCC1):c.1772G>A (p.Ser591Asn)	rs569721834	0.00001
NM_020166.5(MCCC1):c.2172G>A (p.Ser724=)	rs781286566	0.00001
NM_020166.5(MCCC1):c.1662T>C (p.Thr554=)
NM_020166.5(MCCC1):c.1978-8del	rs747001867
NM_020166.5(MCCC1):c.231G>A (p.Ala77=)	rs144230304

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