Table 2 Initial clinical diagnosis and monoallelic variants identified by other approaches in each of the probands included in the study.

From: Searching the second hit in patients with inherited retinal dystrophies and monoallelic variants in ABCA4, USH2A and CEP290 by whole-gene targeted sequencing

Family ID (index)

Clinical diagnosis

Previous variants

Previous studies

Second variant in the same gene

Solved with this panel

A (II:1)

STGD

None

Yes (ABCA4)

B(II:1)

COD

m4:ABCA4 c.466A > G; p.Ile156Val

Complete sequencing by NGS of coding exons of ABCA4 and CRX (External genetics laboratory - Imegen, S.L.)

No

Yes (CNGB3)

C (II:1)

sRP and unilateral maculopathy

m6:ABCA4 c.6148G > C; p.Val2050Leu

Targeted Sequencing Panel30

No

Unknown (FSCN2)

D (II:1)

LCA

None

Yes (LRAT)

E (II:4)

sRP

M9:USH2A c.2276G > T; p.Cys759Phe

Sanger Sequencing of USH2A exon 13

Yes

Yes

F (II:3)

sRP

M9:USH2A c.2276G > T; p.Cys759Phe

Targeted Sequencing Panel30 [Bravo-Gil et al., 2017]

Yes

Yes

G (II:1)

sRP

M9:USH2A c.2276G > T; p.Cys759Phe

Sanger Sequencing of USH2A exon 13

Yes

Yes

H (II:3)

arRP

M9:USH2A c.2276G > T; p.Cys759Phe

Sanger Sequencing of USH2A exon 13

Yes

Yes

I (II:2)

sRP

M9:USH2A c.2276G > T; p.Cys759Phe

Sanger Sequencing of USH2A exon 13

Yes

Yes

J (II:1)

sRP

M9:USH2A c.2276G > T; p.Cys759Phe

Sanger Sequencing of USH2A exon 13

Yes

Yes

K (II:1)

sRP sine pigmento

M9:USH2A c.2276G > T; p.Cys759Phe

Sanger Sequencing of USH2A exon 13

Yes

Yes

L (II:1)

sRP

M9:USH2A c.2276G > T; p.Cys759Phe

Sanger Sequencing of USH2A exon 13

Yes

Yes

M (II:1)

USHER

M17: USH2A c.2299del; p.Glu767Serfs*21

Sanger Sequencing of USH2A exon 13

Yes

Yes

N (II:12)

arRP

M17: USH2A c.2299del; p.Glu767Serfs*21

Genotyping microarray for arRP (584 known variants, Asper Biotech, Ltd)

Yes

Yes

O (II:1)

sRP

M9:USH2A c.2276G > T; p.Cys759Phe

Sanger Sequencing of USH2A exon 13

Yes

Yes

P (II:9)

USHER

M20:USH2A c.907 C > A; p.Arg303Ser

Genotyping microarray for arRP (584 known variants, Asper Biotech, Ltd)

Yes

Yes

Q (II:4)

arRP

M20:USH2A c.907 C > A; p.Arg303Ser

Targeted Sequencing with the same panel as30 [Bravo-Gil et al., 2017]

Yes

Yes

R (II:6)

USHER

None

Yes (USH2A)

S (II:1)

sRP

m33:USH2A c.5363A > G; p.Asp1788Gly

Targeted Sequencing Panel30 [Bravo-Gil et al., 2017]

No

Unknown (USH2A)

T (II:1)

sRP

m26:ABCA4 c.5881G > A; p.Gly1961Arg//m27:CEP290 c.2691A > G; p.Ile897Met

Targeted Sequencing Panel30 [Bravo-Gil et al., 2017]

No

No

U (II:3)

sRP

m28:ABCA4 c.5882G > A p.Gly1961Glu

Targeted Sequencing Panel30 [Bravo-Gil et al., 2017]

No

No

V (II:1)

sRP

m29:ABCA4 c.5908 C > T; p.Leu1970Phe

Targeted Sequencing Panel30 [Bravo-Gil et al., 2017]

No

No

W (II:3)

sRP

m6:ABCA4 c.6148G > C; p.Val2050Leu

Targeted Sequencing Panel30 [Bravo-Gil et al., 2017]

No

No

X (II:1)

sRP

m6:ABCA4 c.6148G > C; p.Val2050Leu

Targeted Sequencing Panel30 [Bravo-Gil et al., 2017]

No

No

Y (II:1)

arRP

m30:CEP290 c.3517C > A p.Gln1173Lys

Targeted Sequencing Panel30 [Bravo-Gil et al., 2017]

No

No

Z (II:1)

sRP

m31:CEP290 c.4237G > C; p.Asp1413His

Targeted Sequencing Panel30 [Bravo-Gil et al., 2017]

No

No

AA (II:4)

sRP

m32:USH2A c.1486A > G; p.Thr496Ala

Targeted Sequencing Panel30 [Bravo-Gil et al., 2017]

No

No

AB (II:1)

STGD

None

No

AC (II:3)

STGD

m4:ABCA4 c.466A > G; p.Ile156Val

Targeted Sequencing Panel30 [Bravo-Gil et al., 2016]

No

No

  1. arRP: Autosomal recessive Retinitis Pigmentosa; COD: Cone Dystrophy; LCA: Leber Congenital Amaurosis; sRP: Simplex RP; STGD: Stargardt disease. Uppercase “M#” indicates likely causal mutations, lowercase “m#” indicates other variants.