Table 2 Number of variants of FAM65A, NFATC3 and CDH23 gene

From: Comprehensive genetic exploration of selective tooth agenesis of mandibular incisors by exome sequencing

Gene

FAM65A

  

NFATC3

CDH23

Affected famili A

       

c.2771G>A

c.244A>G

              

c.4762C>T

   

Affected famili B

       

c.2771G>A

c.244A>G

               

c.5418C>G

  

SH1

 

c.148C>T

                         

SH2

                           

SH3

            

c.127G>A

              

SH4

                           

SH5

                           

SH6

                           

SH7

       

c.2771G>A

                 

c.5722G>A

 

SH9

                           

SH10

                           

SH11

                      

c.4346G>A

    

SH14

             

c.141T>G

             

SH15

            

c.127G>A

              

SH16

                           

SH18

               

c.1681T>G

           

SH19

            

c.127G>A

              

SH21

            

c.127G>A

      

c.3656G>A

       

SH23

                          

c.6023G>T

SH25

c.137C>T

                          

SH26

 

c.148C>T

                         

SH28

                           

SH29

                           

SH31

            

c.127G>A

              

SH32

                 

c.3352G>A

         

SH33

               

c.1681T>G

           

SH34

                

c.3179G>A

          

SH36

                           

SH37

                           

SH38

                           

SH39

                           

SH42

       

c.2771G>A

c.244A>G

                  

SH43

                           

SH44

                           

SH45

                       

c.4762C>T

   

SH47

           

c.1279C>G

               

SH49

                           

SH50

     

c.2668C>T

                     

SH51

            

c.127G>A

    

c.3352G>A

         

SH53

   

c.1994C>T

                       

SH55

c.137C>T

                          

SH56

      

c.2734C>A

  

c.281A>C

c.1043C>T

 

c.127G>A

              

SH58

c.137C>T

                          

SH59

       

c.2771G>A

c.244A>G

                  

SH61

    

c.2542G>A

                      

SH62

                       

c.4762C>T

   

SH63

     

c.2668C>T

 

c.2771G>A

c.244A>G

                  

SH64

     

c.2668C>T

                     

SH68

                    

c.4009G>A

      

SH70

       

c.2771G>A

c.244A>G

                  

SH72

                           

SH75

  

c.1117C>A

                        

SH76

c.137C>T

           

c.127G>A

              

SH77

            

c.127G>A

              

SH78

                           

SH79

c.137C>T

    

c.2668C>T

                     

SH80

              

c.1637G>C

      

c.4135C>T

     

SH81

                  

c.3397G>A

        

SH83

                           
  1. Only individuals with any variants are shown.
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