List of variants in gene OPN1LW studied for perceptual disorders

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_020061.6(OPN1LW):c.920C>T (p.Pro307Leu)	rs782797093	0.00001
NC_000023.11:g.(154153459_154153462)_(154154925_154154928)del
NM_020061.6(OPN1LW):c.1013G>A (p.Gly338Glu)	rs104894913
NM_020061.6(OPN1LW):c.269G>A (p.Trp90Ter)	rs2067071714
NM_020061.6(OPN1LW):c.511G>A (p.Val171Met)	rs5986963
NM_020061.6(OPN1LW):c.513G>T (p.Val171=)	rs5986964
NM_020061.6(OPN1LW):c.607T>C (p.Cys203Arg)	rs121434621
NM_020061.6(OPN1LW):c.739C>T (p.Arg247Ter)	rs104894912
NM_020061.6(OPN1LW):c.764_765del (p.Glu255fs)
NM_020061.6(OPN1LW):c.843G>T (p.Trp281Cys)

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