Skip to main content

Table 2 Genetic mutations identified in this study

From: Consanguinity-based analysis of exome sequencing yields likely genetic causes in patients with inherited retinal dystrophy

ID

Gene

Mutation

Protein change

Transcript

MuationTaster

Poly Phen-2

Sift

CADD

gnomAD

References

F1-III:4

FAM161A

c.1654_1655delAG

p.R552Afs*5

NM_032180.3

D

/

/

/

0

Novel

F2-III:3

RDH12

c.437 T > A

p.V146D

NM_152443.3

D

D

D

27

0.00001193

Gong et al. [34]

F3-III:5

USH2A

c.9469C > T

p.Q3157X

NM_206933.4

D

/

/

37

0.00001631

Jiang et al. [35]

F4-III:4

EYS

c.7228 + 1G > A

splicing

NM_001142800.2

D

/

/

25.9

0.00002783

Gu et al. [36]

F5-III:1

EYS

c.6174 T > G

p.Y2058X

NM_001142800.2

D

/

/

37

0

ClinVar submitted

F6-III:1

USH2A

c.9570 + 1G > A

splicing

NM_206933.4

D

/

/

24.6

0.0000408

Xu et al. [37]

F7-III:4

CRB1

c.3991C > T

p.R1331C

NM_201253.3

D

D

D

32

0.00001989

Tsang et al. [38]

F8-III:5

CEP78

c.830 T > C

p.L277P

NM_032171.3

P

D

D

23.2

0.00003244

Novel

F9-III:2

CYP4V2

c.1091-2A > G

splicing

NM_207352.4

D

/

/

33

0.00004771

Yin et al. [39]

F10-III:1

IQCB1

c.445_448delCTCT

p.L149Sfs*30

NM_001023570.4

D

/

/

/

0

Otto et al. [40]

  1. Homo, homozygous; Mutation Taster-D, disease causing; P, polymorphism; Polyphen-2-D, probably damaging; Sift-D, damaging