Mutation Details for c.3406G>A
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cDNA Name
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c.3406G>A
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Protein Name
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p.Ala1136Thr
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Exon or Intron
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exon 21
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Legacy Exon or Intron
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exon 18
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A1136T
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Other Details
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This mutation was found in a patient with pancreatitis.
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Contributors
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Férec C
2000-09-22
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Institute
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Laboratoire de Biogénétique,
University of Brest
Brest, France
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Submitted Phenotype Details
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The mutation was identified in a patient (male) with pancreatitis, carrying E217G on the other allele. (pers. corr. Ferec)
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Reference
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Férec 2000
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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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