"Genome-Nilou Lab"[submitter] AND "DCC"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1255454	NM_005215.4(DCC):c.67T>C (p.Phe23Leu)	DCC (F23L)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 1255455	NM_005215.4(DCC):c.354G>A (p.Glu118=)	DCC	Single nucleotide variant (synonymous variant)	Mirror movements 1 +2 more	GBenign
Select item 803493	NM_005215.4(DCC):c.601C>G (p.Arg201Gly)	DCC (R201G)	Single nucleotide variant (missense variant)	Mirror movements 1 +2 more	GBenign
Select item 1255456	NM_005215.4(DCC):c.2053+13A>G	DCC	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1255457	NM_005215.4(DCC):c.3108T>C (p.Pro1036=)	DCC	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1255458	NM_005215.4(DCC):c.3130+10A>G	DCC	Single nucleotide variant (intron variant)	not provided +2 more	GBenign

ClinVar