<data>
  <!--   -->
  <variant uri='http://findis.org/internal_id/35'>
     <name scheme='findis'>c.125A&gt;G</name>
     <seq_type>DNA</seq_type>
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Israel-Arab</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='9600239'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.125A&gt;G:c.125A&gt;G</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='X55330' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:c.125A&gt;G:H42R</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='X55330' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/36'>
     <name scheme='findis'>c.136G&gt;A</name>
     <seq_type>DNA</seq_type>
     <ref_seq db='unknown' accession='NM_000481' />
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Caucasian</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='16450403'/>
       <ethnicity db='pubmed' accession='8005589'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.136G&gt;A:c.136G&gt;A</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:c.136G&gt;A:G47R</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/37'>
     <name scheme='findis'>c.434A&gt;T</name>
     <seq_type>DNA</seq_type>
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Caucasian/native american</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='11286506'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.434A&gt;T:c.434A&gt;T</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:c.434A&gt;T:N145I</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/38'>
     <name scheme='findis'>183delC</name>
     <seq_type>DNA</seq_type>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Japanese</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='9621520'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:183delC:183delC</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/39'>
     <name scheme='findis'>c.574C&gt;T</name>
     <seq_type>DNA</seq_type>
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Unknown</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='10873393'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.574C&gt;T:c.574C&gt;T</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:c.574C&gt;T:Q192X</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/40'>
     <name scheme='findis'>c.806G&gt;A</name>
     <seq_type>DNA</seq_type>
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Italian</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='8005589'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.806G&gt;A:c.806G&gt;A</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:c.806G&gt;A:G269D</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/41'>
     <name scheme='findis'>955G&gt;C</name>
     <seq_type>DNA</seq_type>
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Japanese</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='9621520'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:955G&gt;C:955G&gt;C</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:955G&gt;C:D276H</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/42'>
     <name scheme='findis'>IVS7-1G&gt;A</name>
     <seq_type>DNA</seq_type>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Mexican Hispanic</population>
       <population>Portuguese</population>
       <population>Spanish</population>
       <population>Dutch</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='11139253'/>
       <ethnicity db='pubmed' accession='11286506'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:IVS7-1G&gt;A:IVS7-1G&gt;A</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/43'>
     <name scheme='findis'>c.959G&gt;A</name>
     <seq_type>DNA</seq_type>
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Anglo-European</population>
       <population>Dutch/Spanish</population>
       <population>Portugese</population>
       <population>Caucasian</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='10873393'/>
       <ethnicity db='pubmed' accession='8005589'/>
       <ethnicity db='pubmed' accession='11139253'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.959G&gt;A:c.959G&gt;A</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:c.959G&gt;A:R320H</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/44'>
     <name scheme='findis'>c.887G&gt;A</name>
     <seq_type>DNA</seq_type>
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Mexican Hispanic</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='12948742'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.887G&gt;A:c.887G&gt;A</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:c.887G&gt;A:R296H</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/45'>
     <name scheme='findis'>GTG&gt;GCG</name>
     <seq_type>DNA</seq_type>
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Unknown</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='12948742'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:GTG&gt;GCG:GTG&gt;GCG</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:GTG&gt;GCG:V212A</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/46'>
     <name scheme='findis'>TAC&gt;TGC</name>
     <seq_type>DNA</seq_type>
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Unknown</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='12948742'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:TAC&gt;TGC:TAC&gt;TGC</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:TAC&gt;TGC:Y225C</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/47'>
     <name scheme='findis'>c.217C&gt;T</name>
     <seq_type>DNA</seq_type>
     <ref_seq db='unknown' accession='NM_000481' />
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Caucasian</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='16450403'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.217C&gt;T:c.217C&gt;T</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:c.217C&gt;T:R73C</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/48'>
     <name scheme='findis'>c.230C&gt;T</name>
     <seq_type>DNA</seq_type>
     <ref_seq db='unknown' accession='NM_000481' />
     <consequence>
       <consequence></consequence>
     </consequence>
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Caucasian</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='16450403'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.230C&gt;T:c.230C&gt;T</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
      <variant>
         <name scheme='findis'>AMT:c.230C&gt;T:S77L</name>
         <seq_type>Protein</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/49'>
     <name scheme='findis'>c.60delG</name>
     <seq_type>DNA</seq_type>
     <ref_seq db='unknown' accession='NM_000481' />
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Caucasian</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='16450403'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.60delG:c.60delG</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/50'>
     <name scheme='findis'>c.61delC</name>
     <seq_type>DNA</seq_type>
     <ref_seq db='unknown' accession='NM_000481' />
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Oriental</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='16450403'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.61delC:c.61delC</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/51'>
     <name scheme='findis'>c.147delG</name>
     <seq_type>DNA</seq_type>
     <ref_seq db='unknown' accession='NM_000481' />
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Oriental</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='16450403'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.147delG:c.147delG</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/52'>
     <name scheme='findis'>c.452_466del</name>
     <seq_type>DNA</seq_type>
     <ref_seq db='unknown' accession='NM_000481' />
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Caucasian</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='16450403'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.452_466del:c.452_466del</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/53'>
     <name scheme='findis'>c.970_972delATG</name>
     <seq_type>DNA</seq_type>
     <ref_seq db='unknown' accession='NM_000481' />
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Oriental</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='16450403'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.970_972delATG:c.970_972delATG</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/54'>
     <name scheme='findis'>c.982_972GC&gt;T</name>
     <seq_type>DNA</seq_type>
     <ref_seq db='unknown' accession='NM_000481' />
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Caucasian</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='16450403'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.982_972GC&gt;T:c.982_972GC&gt;T</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/55'>
     <name scheme='findis'>c.471+2T&gt;C</name>
     <seq_type>DNA</seq_type>
     <ref_seq db='unknown' accession='NM_000481' />
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Caucasian</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='16450403'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.471+2T&gt;C:c.471+2T&gt;C</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
  <!--   -->
  <variant uri='http://findis.org/internal_id/56'>
     <name scheme='findis'>c.535delC</name>
     <seq_type>DNA</seq_type>
     <ref_seq db='unknown' accession='NM_000481' />
     <phenotypes>
      <phenotype accession='NKH'>
         Nonketotic hyperglycinemia
      </phenotype>
     </phenotypes>
     <populations> 
       <population>Oriental</population>
     </populations> 
     <publications>
       <ethnicity db='pubmed' accession='16450403'/>
     </publications>
     <seq_change>
      <variant>
         <name scheme='findis'>AMT:c.535delC:c.535delC</name>
         <seq_type>DNA</seq_type>
         <ref_seq db='unknown' accession='NM_000481' />
      </variant>
     </seq_change>
  </variant>
</data>
