Mutation Details for c.3835_3836delTT
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cDNA Name
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c.3835_3836delTT
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Protein Name
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p.Leu1279AlafsX22
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Exon or Intron
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exon 23
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Other Details
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The patient is compound heterozygote, the second mutation is F508del; the mutation was detected after sequencing of the whole CFTR gene and was detected only once in our cohort of CF-patients
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Contributors and Institutes
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| Wagner Klaus | - | Medical University Graz, Institute of Human Genetics |
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Submitted Phenotype Details
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The female patient was born 2007, parents are from Austria and father showed the same allele. Sweat test was repeatedly positive
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Reference
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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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