"Genome-Nilou Lab"[submitter] AND "UNC13D"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 263240	NM_199242.3(UNC13D):c.3198A>G (p.Glu1066=)	UNC13D	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 263236	NM_199242.3(UNC13D):c.2830+37C>G	LOC112533672, UNC13D	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 263228	NM_199242.3(UNC13D):c.2599A>G (p.Lys867Glu)	UNC13D (K867E)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 263222	NM_199242.3(UNC13D):c.1992+5G>A	UNC13D	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 263212	NM_199242.3(UNC13D):c.1389+36G>A	UNC13D	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 263247	NM_199242.3(UNC13D):c.888G>C (p.Pro296=)	UNC13D	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 263214	NM_199242.3(UNC13D):c.154-19G>A	UNC13D	Single nucleotide variant (intron variant)	not specified +2 more	GBenign

ClinVar