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. 2019 Nov 12;9:16576. doi: 10.1038/s41598-019-51768-8

Table 2.

Genetic findings in 12 children with ocular features of albinism and no obvious skin pigmentation abnormalities.

proband ID gene panel used for testing (number of genes evaluated) variant 1 variant 2 variant 3 samples available for segregation
1 ocular/oculocutanous albinism (18) GPR143 c.659-1 G > A mother
2 nystagmus & foveal hypoplasia (26) SLC38A8 c.534 C > G p.(Ile178Met) SLC38A8 exon 2 to 5 deletion none
3 ocular/oculocutanous albinism (18) TYR c.1217 C > T p.(Pro406Leu) TYR c.575 C > A p.(Ser192Tyr) TYR 1205 G > A p.(Arg402Gln) none
4 optic nerve disorders (40) TYR c.1118 C > A p.(Thr373Lys) TYR c.575 C > A p.(Ser192Tyr) TYR 1205 G > A p.(Arg402Gln) mother & father
5 ocular/oculocutanous albinism (18) TYR c.823 G > T p.(Val275Phe) TYR c.[575 C > A; 1205 G > A] p.[(Ser192Tyr);(Arg402Gln)] OCA2 c.1327 G > A p.(Val443Ile) mother & father
6 nystagmus & foveal hypoplasia (26) TYR c.1118 C > A p.(Thr373Lys) TYR c.[575 C > A; 1205 G > A] p.[(Ser192Tyr);(Arg402Gln)] mother & father
7 nystagmus & foveal hypoplasia (26) TYR c.[575 C > A; 1205 G > A] p.[(Ser192Tyr);(Arg402Gln)] TYR c.[575 C > A; 1205 G > A] p.[(Ser192Tyr);(Arg402Gln)] no
8 ocular/oculocutanous albinism (18) TYR c.[575 C > A; 1205 G > A] p.[(Ser192Tyr);(Arg402Gln)] TYR c.[575 C > A; 1205 G > A] p.[(Ser192Tyr);(Arg402Gln)] TYRP1 c.208 G > A p.(Ala70Thr) mother, father & affected brother
9 clinical exome OCA2 c.1327 G > A p.(Val443Ile) TYR c.575 C > A p.(Ser192Tyr) TYR 1205 G > A p.(Arg402Gln) no
10 nystagmus & foveal hypoplasia (26) OCA2 c.2346deIG p.(Thr783Hisfs*2) TYR c.1392dupT p.(Lys465*) mother
11 nystagmus & foveal hypoplasia (26) OCA2 c.1441 G > A, (p.Ala481Thr) TYR c.1217 C > T, p.(Pro406Leu) mother
12 ocular/oculocutanous albinism (18) no pathogenic variant identified no

The genes and transcripts included in each gene panel can be found in Supplementary Table 1. The results of segregation are discussed in the text and family trees are provided in the Supplementary File.