Mutation Details for c.869+11C>T
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cDNA Name
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c.869+11C>T
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Exon or Intron
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intron 7
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Legacy Exon or Intron
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intron 6b
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1001+11C/T
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Other Details
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The 1001+11C->T polymorphism in intron 6b was found in 19 out of 63 unrelated Belgian CF chromosomes.
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Contributors
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Cuppens H,
Marynen P,
Cassiman JJ
1991-11-15
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Institute
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University of Leuven
Leuven, Belgium
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Submitted Phenotype Details
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This is a frequent polymorphism. No additional clinical data available. (pers. corr. Cuppens)
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Reference
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Cuppens et al. (NL #40)
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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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