"Clinical Genetics, Academic Medical Center"[submitter] AND "DDC"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 360429	NM_001082971.2(DDC):c.1385G>A (p.Arg462Gln)	DDC (R462Q +4 more)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 360434	NM_001082971.2(DDC):c.649A>G (p.Met217Val)	DDC (M217V +2 more)	Single nucleotide variant (missense variant +1 more)	Deficiency of aromatic-L-amino-acid decarboxylase +1 more	GBenign
Select item 235399	NM_001082971.2(DDC):c.629C>T (p.Pro210Leu)	DDC (P210L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GBenign/Likely benign
Select item 518386	NM_001082971.2(DDC):c.436-12T>C	DDC	Single nucleotide variant (intron variant)	Deficiency of aromatic-L-amino-acid decarboxylase +1 more	GBenign/Likely benign
Select item 518387	NM_001082971.2(DDC):c.436-16C>T	DDC	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 360442	NM_001082971.2(DDC):c.96C>T (p.Asp32=)	DDC	Single nucleotide variant (synonymous variant)	Deficiency of aromatic-L-amino-acid decarboxylase +1 more	GBenign/Likely benign
Select item 1168240	NM_001082971.2(DDC):c.49A>G (p.Met17Val)	DDC (M17V)	Single nucleotide variant (missense variant)	Deficiency of aromatic-L-amino-acid decarboxylase	GBenign

ClinVar