List of variants reported as uncertain significance for retinitis pigmentosa 51

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_144596.4(TTC8):c.1327C>T (p.Arg443Trp)	rs140698625	0.00064
NM_144596.4(TTC8):c.1262G>C (p.Arg421Thr)	rs374742528	0.00021
NM_144596.4(TTC8):c.433G>A (p.Ala145Thr)	rs540856754	0.00010
NM_144596.4(TTC8):c.1294G>A (p.Glu432Lys)	rs114401181	0.00009
NM_144596.4(TTC8):c.905A>G (p.Tyr302Cys)	rs370111364	0.00008
NM_144596.4(TTC8):c.308G>T (p.Gly103Val)	rs140710339	0.00007
NM_144596.4(TTC8):c.1051C>T (p.Arg351Trp)	rs755412340	0.00006
NM_144596.4(TTC8):c.4A>G (p.Ser2Gly)	rs759112760	0.00006
NM_144596.4(TTC8):c.874G>A (p.Val292Ile)	rs375086490	0.00006
NM_144596.4(TTC8):c.913A>G (p.Met305Val)	rs143237548	0.00006
NM_144596.4(TTC8):c.1078G>A (p.Gly360Ser)	rs771231605	0.00005
NM_144596.4(TTC8):c.800T>A (p.Val267Asp)	rs770333148	0.00004
NM_144596.4(TTC8):c.980A>G (p.Glu327Gly)	rs749721461	0.00003
NM_144596.4(TTC8):c.43T>C (p.Phe15Leu)	rs1379428942	0.00002
NM_144596.4(TTC8):c.607G>A (p.Glu203Lys)	rs1018209116	0.00002
NM_144596.4(TTC8):c.855A>C (p.Leu285Phe)	rs774379732	0.00002
NM_144596.4(TTC8):c.988G>A (p.Ala330Thr)	rs568563702	0.00002
NM_144596.4(TTC8):c.1133T>C (p.Met378Thr)	rs1003053014	0.00001
NM_144596.4(TTC8):c.1215T>G (p.His405Gln)	rs753212470	0.00001
NM_144596.4(TTC8):c.1363C>A (p.Gln455Lys)	rs773278542	0.00001
NM_144596.4(TTC8):c.1402C>T (p.His468Tyr)	rs148602884	0.00001
NM_144596.4(TTC8):c.145-10T>C	rs754997963	0.00001
NM_144596.4(TTC8):c.452T>A (p.Ile151Asn)	rs774233751	0.00001
NM_144596.4(TTC8):c.488C>T (p.Thr163Met)	rs758942370
NM_144596.4(TTC8):c.983C>T (p.Ala328Val)	rs755533153

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