"PreventionGenetics, part of Exact Sciences"[submitter] AND "CD207"[ge - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3060971	NM_015717.5(CD207):c.984G>A (p.Pro328=)	CD207, LOC126806248	Single nucleotide variant (synonymous variant)	CD207-related disorder	GBenign
Select item 3060627	NM_015717.5(CD207):c.942G>A (p.Thr314=)	CD207, LOC126806248	Single nucleotide variant (synonymous variant)	CD207-related disorder	GBenign
Select item 3059640	NM_015717.5(CD207):c.833T>C (p.Val278Ala)	CD207, LOC126806248 (V278A)	Single nucleotide variant (missense variant)	CD207-related disorder	GBenign
Select item 3059699	NM_015717.5(CD207):c.711T>C (p.Ser237=)	CD207	Single nucleotide variant (synonymous variant)	CD207-related disorder	GBenign
Select item 3060755	NM_015717.5(CD207):c.406C>G (p.Gln136Glu)	CD207 (Q136E)	Single nucleotide variant (missense variant)	CD207-related disorder	GBenign
Select item 3060821	NM_015717.5(CD207):c.341A>T (p.Glu114Val)	CD207 (E114V)	Single nucleotide variant (missense variant)	CD207-related disorder	GBenign
Select item 3060462	NM_015717.5(CD207):c.234C>T (p.Val78=)	CD207	Single nucleotide variant (synonymous variant)	CD207-related disorder	GBenign
Select item 3049037	NM_015717.5(CD207):c.183C>T (p.Ala61=)	CD207	Single nucleotide variant (synonymous variant)	CD207-related disorder	GLikely benign
Select item 3059383	NM_015717.5(CD207):c.164C>T (p.Ala55Val)	CD207 (A55V)	Single nucleotide variant (missense variant)	CD207-related disorder	GBenign