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. 2017 May 5;130(9):1049–1054. doi: 10.4103/0366-6999.204925

Table 2.

GJB1 mutations in 22 CMT1X patients from unrelated families in this study

Patient number Nucleotide changes Amino acid changes Domain Novel mutation
1 c.44G>T R15L N-terminal domain No
2 c.59T>G I20T N-terminal domain No
3 c.62G>A G21D N-terminal domain No
4 c.115G>T A39S TM1 Yes
5 c.194A>G Y65C EC1 No
6 c.263C>A A88D TM2 Yes
7 c.379A>T I127F IC Yes
8 c.380T>A I127N IC No
9 C.403_404insT Y135fsX146 TM3 No
10 c.424C>T R142W TM3 No
11 c.424C>T R142W TM3 No
12 c.425G>A R142Q TM3 No
13 c.425G>A R142Q TM3 No
14 c.490C>T R164W EC2 No
15 c.533A>G D178G EC2 No
16 c.548G>A R183H EC2 No
17 c.548G>A R183H EC2 No
18 c.547C>T R183C EC2 No
19 c.556G>A E186K EC2 No
20 c.590C>T A197V TM4 No
21 c.614A>G N205S TM4 No
22 c.818_819insGGGCT L273fs C-terminal domain Yes

CMT1X: X-linked Charcot-Marie-Tooth type 1; EC: Extracellular domain; TM: Transmembrane domain; IC: Intracellular loop; GJB1: Gap junction beta-1 protein.