Table 1.
Family | Diagnosis | Gene | Allele 1a |
Allele 1 predicted |
Allele 2b |
Allele 2 predicted |
Pathogenicity |
Pathogenicity |
Ethnicityc |
---|---|---|---|---|---|---|---|---|---|
protein changea | protein changeb | allele 1a | allele 2b | ||||||
46 |
USH2 |
USH2A |
c.6862G>T |
p.(Glu2288*) |
exon 40 deleted c.7452-68_7594+942del |
p.(Leu2485Thrfs*25) |
Pathogenic |
Pathogenic |
Caucasian |
148 |
USH2 |
USH2A |
c.2299delG |
p.(Glu767Serfs*21) |
exon 27 deleted c.[5299-932_5572+1023del; 5572+1100_5573-1099del] |
p.(Met1767Valfs*6) |
Pathogenic |
Pathogenic |
Caucasian |
151 |
USH2 |
USH2A |
c.3187_3188delCA |
p.(Gln1063Serfs*15) |
exon 22–23 deleted c.4628-15914_4885+472del |
p.(Ile1544_Gly1629del) |
Pathogenic |
Pathogenic |
Caucasian |
309 |
USH2 |
USH2A |
c.2299delG |
p.(Glu767Serfs*21) |
exon 4 deleted c.781_784+1375del |
p.? |
Pathogenic |
Pathogenic |
Caucasian |
657 |
USH2 |
USH2A |
c.187C>T |
p.(Arg63*) |
exon 70 deleted c.15053-26_15298-708del |
p.(Leu5019Valfs*77) |
Pathogenic |
Pathogenic |
Caucasian |
283 |
USH2 |
USH2A |
c.2299delG |
p.(Glu767Serfs*21) |
exons 4–13 duplicated |
p.? |
Pathogenic |
Pathogenic |
Caucasian |
24 |
USH2 |
USH2A |
c.2299delG |
p.(Glu767Serfs*21) |
c.7595-2144A>G |
p.(Lys2532Thrfs*56) |
Pathogenic |
Pathogenic |
Caucasian |
707 |
USH2 |
USH2A |
c.2299delG |
p.(Glu767Serfs*21) |
c.7595-2144A>G |
p.(Lys2532Thrfs*56) |
Pathogenic |
Pathogenic |
Caucasian |
128 | Atypical Usher | USH2A | Unknown | Unknown | c.7595-2144A>G | p.(Lys2532Thrfs*56) | Pathogenic |
Variants in bold are novel mutations, identified in this study.
a All allele 1 variants have been previously published in these individuals [7].
b All allele 2 variants were identified in this study by USH2A MLPA or sequencing for USH2A: c.7595-2144A>G.
c Caucasian represents UK and European.