I am using exome seq to search for causative mutations in a family with Mendel type genetic disease.
A mutation was found in all the patients while absent among normal people of the pedigree. function of the gene is strongly supporting the phenotype of the disease.
however, the mutation has been reported in the 1000 genome project, although in a very low frequency(1 out of 1094). clinical features of the disease is very mild, only affecting skin pigment distribution.
my questions are:
Does this mutation worth further investigation?
If does, what should I do?
thanks for you attention.
A mutation was found in all the patients while absent among normal people of the pedigree. function of the gene is strongly supporting the phenotype of the disease.
however, the mutation has been reported in the 1000 genome project, although in a very low frequency(1 out of 1094). clinical features of the disease is very mild, only affecting skin pigment distribution.
my questions are:
Does this mutation worth further investigation?
If does, what should I do?
thanks for you attention.
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