Mutation Details for c.259T>A

cDNA Name c.259T>A 
Protein Name p.Phe87Ile 
Exon or Intron exon 3 
Other Details The above mutation was identified by SSCP analysis and characterized by direct DNA sequencing. This mutation was detected in infertile male with congenital bilateral absence of vas deferens. Mutation on other allele was Delta F508 mutation. This mutation was not found on 100 non-CF chromosomes. 
Contributors and Institutes
Sharma N - Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Acharya N - Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Singh SK - Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Singh M - Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Kaur G - Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Prasad R - Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  
Submitted Phenotype Details This is a case of 32 year old infertile male married for 8 years. His sweat chloride was 88 mEq/L, Testosterone- 250ng/dl, FSH- 3.8 mIU/ml, LH- 4.3mIU/ml, Urea- 28 mg/dl and Creatinine- 0.9mg/dl. Semen analysis demonstrated nil sperm count and FNAC revealed normal spermatogenesis. Transrectal ultrasound and abdominal ultrasonography showed no other urogenital malformation. Chest X-ray was normal. However, on physical examination congenital bilateral absence of vas deferens was reported (pers. corr. Prasad). 
Reference  

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The Database was last updated at Apr 25, 2011