List of variants reported as benign for Usher syndrome type 1F by Genome-Nilou Lab

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Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_001384140.1(PCDH15):c.2869-109T>C	rs2456699	0.77156
NM_001384140.1(PCDH15):c.3374-72A>G	rs2593124	0.75471
NM_001384140.1(PCDH15):c.705+93C>T	rs857395	0.74876
NM_001384140.1(PCDH15):c.3374-68T>G	rs10740559	0.74015
NM_001384140.1(PCDH15):c.706-8C>T	rs10740579	0.71606
NM_001384140.1(PCDH15):c.986-81C>T	rs10763086	0.71010
NM_001384140.1(PCDH15):c.3010-48G>A	rs2593107	0.70086
NM_001384140.1(PCDH15):c.2751+37C>T	rs3812658	0.59606
NM_001384140.1(PCDH15):c.92-52T>G	rs10825347	0.50625
NM_001384140.1(PCDH15):c.4367+119T>C	rs10740555	0.43920
NM_001384140.1(PCDH15):c.4203-151C>A	rs4935096	0.38898
NM_001384140.1(PCDH15):c.4203-162T>C	rs4935472	0.38838
NM_001384140.1(PCDH15):c.3984-20C>T	rs7089209	0.37411
NM_001384140.1(PCDH15):c.3717+35T>C	rs10825135	0.35243
NM_001384140.1(PCDH15):c.594+232A>G	rs2153822	0.26148
NM_001384140.1(PCDH15):c.1263T>C (p.Thr421=)	rs7921598	0.23801
NM_001384140.1(PCDH15):c.1138G>A (p.Gly380Ser)	rs10825269	0.22813
NM_001384140.1(PCDH15):c.2786G>A (p.Arg929Gln)	rs2135720	0.22399
NM_001384140.1(PCDH15):c.2220+47T>C	rs3812657	0.22115
NM_001384140.1(PCDH15):c.55T>G (p.Ser19Ala)	rs11004439	0.20535
NM_001384140.1(PCDH15):c.319-31T>C	rs11594958	0.20278
NM_001384140.1(PCDH15):c.5156A>C (p.Gln1719Pro)	rs17704703	0.20017
NM_001384140.1(PCDH15):c.1306-4123C>T	rs16905686	0.17435
NM_001384140.1(PCDH15):c.4671+1344A>C	rs11003863	0.17427
NM_001384140.1(PCDH15):c.1304A>C (p.Asp435Ala)	rs4935502	0.15952
NM_033056.4(PCDH15):c.4581C>A (p.Pro1527=)	rs10825114	0.12444
NM_001384140.1(PCDH15):c.157+3A>G	rs41274636	0.09581
NM_001384140.1(PCDH15):c.2752-75C>G	rs2253647	0.07354
NM_001384140.1(PCDH15):c.1591-68G>A	rs41274632	0.07262
NM_001384140.1(PCDH15):c.2868+69G>A	rs11003980	0.05390
NM_001384140.1(PCDH15):c.1910A>G (p.Asn637Ser)	rs61731389	0.02908
NM_001384140.1(PCDH15):c.3718-19C>A	rs75248212	0.02141
NM_001384140.1(PCDH15):c.546A>G (p.Gly182=)	rs34164469	0.01517
NM_001384140.1(PCDH15):c.4367+88A>G	rs45466098	0.00811
NM_033056.4(PCDH15):c.4850A>G (p.Asn1617Ser)	rs111033362	0.00631
NM_001384140.1(PCDH15):c.1590+20A>G	rs7093302
NM_001384140.1(PCDH15):c.1917+13GT[10]	rs5785040
NM_001384140.1(PCDH15):c.3502-14dup	rs5785023

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