"Genome-Nilou Lab"[submitter] AND "AP4M1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1192439	NM_004722.4(AP4M1):c.147+35T>C	AP4M1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 678005	NM_004722.4(AP4M1):c.462+34G>A	AP4M1	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 50 +2 more	GBenign
Select item 1192440	NM_004722.4(AP4M1):c.544-75T>C	AP4M1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 680070	NM_004722.4(AP4M1):c.1025+44T>C	AP4M1	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 50 +1 more	GBenign
Select item 1260154	NM_004722.4(AP4M1):c.*322A>G	AP4M1, TAF6	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 712377	NM_139315.3(TAF6):c.1904C>T (p.Pro635Leu)	AP4M1, TAF6 (P672L +3 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GBenign

ClinVar