List of variants in gene DCC reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_005215.4(DCC):c.1409G>A (p.Gly470Asp)	rs141813053	0.00296
NM_005215.4(DCC):c.2105A>G (p.Asn702Ser)	rs35691189	0.00284
NM_005215.4(DCC):c.1743A>G (p.Leu581=)	rs148819965	0.00071
NM_005215.4(DCC):c.1157G>A (p.Arg386Gln)	rs140711456	0.00014
NM_005215.4(DCC):c.2000G>A (p.Arg667His)	rs200099519	0.00013
NM_005215.4(DCC):c.4255-187A>G	rs753489837	0.00001
NM_005215.4(DCC):c.120G>A (p.Leu40=)
NM_005215.4(DCC):c.1256A>G (p.Lys419Arg)	rs144623089
NM_005215.4(DCC):c.1572G>A (p.Glu524=)
NM_005215.4(DCC):c.1821C>T (p.Gly607=)
NM_005215.4(DCC):c.2631G>A (p.Glu877=)
NM_005215.4(DCC):c.3399G>A (p.Arg1133=)
NM_005215.4(DCC):c.3741C>T (p.Val1247=)
NM_005215.4(DCC):c.549C>T (p.Ile183=)
NM_005215.4(DCC):c.706C>T (p.Leu236=)
NM_005215.4(DCC):c.783T>C (p.Cys261=)

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