"Genome-Nilou Lab"[submitter] AND "ZNF454"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 99643	NM_000843.4(GRM6):c.2196G>A (p.Thr732=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 99629	NM_000843.4(GRM6):c.1500+23A>G	GRM6, ZNF454	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 99628	NM_000843.4(GRM6):c.1392A>G (p.Gly464=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 99627	NM_000843.4(GRM6):c.1353T>C (p.Asn451=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 198105	NM_000843.4(GRM6):c.1308T>C (p.Thr436=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	Congenital stationary night blindness 1B +2 more	GBenign
Select item 99626	NM_000843.4(GRM6):c.1227C>T (p.Tyr409=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 99625	NM_000843.4(GRM6):c.1131C>T (p.Asp377=)	ZNF454, GRM6	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign

ClinVar