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. 2011 May 11;6:21. doi: 10.1186/1750-1172-6-21

Table 1.

Genotypes of USH patients

Genes MYO7A USH1C CDH23 PCDH15 USH1G USH2A VLGR1 WHRN USH3A
Patient USH type

U37 I [p.R666X] + [p.E1917X]

U57 I [p.C1198X]+ [p.R1240Q]

P0485 I [p.Q1798X] + [p.E1917X]

U14 C I [p.R972X] + [p.R972X]

U9 C I [p.K164X] + [p.K164X]

U36 I [p.R2024X] + [p.G519D] [p.R1060W]

U20 I [p.R669X] + [p.R1883Q]

P0505 I [p.Q1798X] + [p.A2009fsX32]

S1556 C I [p.H133fsX7] + [p.H133fsX7]

S1295 C I [p.Y1302fsX97] + [p.Y1302sX97] [p.G1301V] [p.Q5459H]

P0504 I [p.D75fsX31] + [p.R1240Q] [p.R357W]

U45 I [p.D75fsX31] + [p.T165M]

P0411 C I [c.2283-1G>T] + [c.2283-1G>T] [p.D4707Y]

P0070 I [p.G163R] + [p.A198T]

P0052 I [c.1690+1G>A] + [p.F1963del]

U3 I [p.L2186P] [p.L16V] [p.C3307W]

DID C I [p.R80fsX69] + [p.R80fsX69] [p.R3043W]

U47 I [p.R80fsX69] + [p.R103H]

P0469 I [p.E2135fsX3] + [c.6050-9G>A]

S1212 I [p.R1379P] + [p.D2639G]

U38 I [p.R991X] + [p.R991X]

S1530 I [p.R1273S]

P0257 I [p.W38X]

S1273 I [p.D29fsX29] + [p.D29fsX29]

U46 I

U50 I

S1823 C I


P0486 II [p.A457V] +
[p.K269del]

U6 II [p.E3562X] + [p.E767fsX21]

U24 II [p.P1220L] [p.S1307X] + [p.C536R]

U48 II [p.W3955X] + [p.R2509fsX19]

P0483 II [p.E1492X] + [p.T3571M]

P0418 II [p.K268R] [p.S5030X]

U56 C II [p.T2991fsX61] + [p.T2991fsX61]

U42 II [p.E767fsX21] + [p.Y4128fsX24]

P0449 II [p.E767fsX21] + [p.C575Y]

P0493 II [p.H308fsX16] + [p.T4809I]

P0432 II [p.R1189W] [p.M1344fsX42]

U51 II [p.V218E] + [p.R317R]

P0511 II [p.T3571M] + [p.T352I]

U49 II [p.E4321X] + [p.Q753fsX8]

P0473 II [p.P522fsX8] + [p.M5890fsX10] [p.S11R]

U58 II [p.F112fsX29] + [p.H3399P]

P0463 II [p.E4186fsX17]

U10 II

U53 II [p.P246fsX13] + [p.P246fsX13]

U19 C II [p.H755Y]

P0426 II


U21 III [p.Y1730fsX6] + [c.10586-1G>C]

U30 III [p.E767fsX21] + [p.R303H]

S1226 III [p.G2752R] + [c.5776+1G>A]

P0239 III [p.N4885S]

P0484 III [p.D1944N]

P0069 III [p.R379W]

Novel mutations are in bold. C (2nd column) denotes consanguinity.