Mutation Details for c.3918C>T
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cDNA Name
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c.3918C>T
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Exon or Intron
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exon 24
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Legacy Exon or Intron
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exon 21
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P1306P (4050C/T)
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Other Details
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no change (Pro at 1306)
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Contributors
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Ferec C,
Quere I,
Audrezet MP,
Verlingue C,
Guillermit H,
Mercier B,
Raguenes O
1993-01-19
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Institute
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Centre de Transfusion Sanguine et de Biogenetique
Brest, France
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Submitted Phenotype Details
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P1306P is a polymorphism. No clinical data available. (pers.corr. Ferec)
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Reference
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Férec et al. (NL#52)
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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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