Mutation Details for c.895G>A
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cDNA Name
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c.895G>A
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Protein Name
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p.Ala299Thr
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Exon or Intron
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exon 8
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Legacy Exon or Intron
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exon 7
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A299T
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Other Details
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Asymptomatic subject.
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Contributors
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Férec C
1999-01-01
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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 an individual with neonatal hypertrypsinemia. (pers.corr. Ferec)
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Reference
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Férec 1999
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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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