List of variants studied for retinitis pigmentosa 88 by Fulgent Genetics, Fulgent Genetics

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_178857.6(RP1L1):c.844A>C (p.Asn282His)	rs75814156	0.02124
NM_178857.6(RP1L1):c.1478G>A (p.Arg493Gln)	rs79401306	0.02007
NM_178857.6(RP1L1):c.1691C>G (p.Ser564Cys)	rs77585543	0.00860
NM_178857.6(RP1L1):c.3955G>A (p.Ala1319Thr)	rs73201156	0.00515
NM_178857.6(RP1L1):c.444T>G (p.Leu148=)	rs112609335	0.00208
NM_178857.6(RP1L1):c.954C>T (p.Asp318=)	rs200317816	0.00031
NM_178857.6(RP1L1):c.455G>A (p.Arg152Gln)	rs200213603	0.00030
NM_178857.6(RP1L1):c.3201C>T (p.Gly1067=)	rs200462441	0.00023
NM_178857.6(RP1L1):c.5132G>C (p.Gly1711Ala)	rs200635063	0.00019
NM_178857.6(RP1L1):c.4482A>G (p.Gln1494=)	rs201357374	0.00011
NM_178857.6(RP1L1):c.1189C>T (p.Arg397Ter)	rs371886218	0.00005
NM_178857.6(RP1L1):c.202C>T (p.Leu68Phe)	rs902459185	0.00001
NM_178857.6(RP1L1):c.2499G>A (p.Pro833=)	rs373310698
NM_178857.6(RP1L1):c.3710A>G (p.Gln1237Arg)
NM_178857.6(RP1L1):c.3956_4003del (p.Ala1319_Glu1334del)	rs746122572
NM_178857.6(RP1L1):c.5673G>C (p.Glu1891Asp)

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