Mutation Details for c.3468+42G>A
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cDNA Name
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c.3468+42G>A
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Exon or Intron
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intron 21
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Legacy Exon or Intron
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intron 18
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3600+42G/A
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Other Details
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The intron 18 variant was only observed once in an individual suspected to have CF.
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Contributors
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Dörk T,
El-Harith E-H A,
Schmidtke J,
Stuhrmann M
1996-11-21
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Institute
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Institut fur Humangenetik,
Medizinische Hachschule Hannover,
Hannover, Germany
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Submitted Phenotype Details
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Reference
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Dörk et al. (NL#69)
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To check if there are any papers published about this mutation/variant on PubMed, please click here.
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