Mutation Details for c.489+31C>G
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cDNA Name
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c.489+31C>G
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Exon or Intron
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intron 4
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Legacy Exon or Intron
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intron 4
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621+31C/G
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Other Details
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This polymorphism was seen in a Pakistani individual with no known family history of cystic fibrosis.
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Contributors
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Andrew N,
Malone G,
Schwarz M
1999-09-02
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Institute
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Royal Manchester Children's Hospital,
England
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Submitted Phenotype Details
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Reference
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Andrew et al. 1999
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