"Genome-Nilou Lab"[submitter] AND "TRPM1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 315490	NM_001252024.2(TRPM1):c.4560T>A (p.His1520Gln)	TRPM1 (H1498Q +2 more)	Single nucleotide variant (missense variant)	Congenital stationary night blindness 1C +1 more	GBenign
Select item 315497	NM_001252024.2(TRPM1):c.4201C>A (p.Pro1401Thr)	TRPM1 (P1379T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 315498	NM_001252024.2(TRPM1):c.4189G>T (p.Glu1397Ter)	TRPM1 (E1375* +2 more)	Single nucleotide variant (nonsense)	not provided +1 more	GBenign
Select item 315511	NM_001252024.2(TRPM1):c.2406T>C (p.Asn802=)	TRPM1	Single nucleotide variant (synonymous variant)	Congenital stationary night blindness 1C +1 more	GBenign
Select item 193856	NM_001252024.2(TRPM1):c.1305G>A (p.Thr435=)	TRPM1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 196343	NM_001252024.2(TRPM1):c.161G>A (p.Ser54Asn)	TRPM1 (S32N +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 315540	NM_001252024.2(TRPM1):c.68T>C (p.Met23Thr)	TRPM1 (M1T +2 more)	Single nucleotide variant (missense variant +1 more)	Congenital stationary night blindness 1C +1 more	GBenign
Select item 1227039	NM_001252024.2(TRPM1):c.4-36G>A	TRPM1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

ClinVar