Instructions: Enter a mutation entry in HGBase format or select from samples below. When done, click on the SUBMIT button. The script will extract individual data elements from your input.

MUTATION ENTRY:

Sample Input:

HaplotypeID HAP000000001 Allele SNP000006633.ALE000010573: G Allele SNP000006216.ALE000009739: G IsInBlock No (SRC000000969) XX Observation PopulationID POP000000142 Population Caucasian (216 individuals) Frequency 96 % (159 individuals) XX SourceID SRC000000969 Citation Koper JW, et al, Hum Genet 99:663-668, 1997 Submitter Jan W. Koper (SUB000000136) SourceComment Submitted data (27-02-2002) from published studies MeSH Aged MeSH Amino Acid Sequence MeSH Base Sequence MeSH Blood Pressure MeSH Body Constitution MeSH Body Mass Index MeSH Chronic Disease MeSH Codon MeSH Drug Resistance/genetics* MeSH Exons MeSH Female MeSH Glucocorticoids/pharmacology* MeSH Human MeSH Male MeSH Middle Age MeSH Netherlands MeSH Polymerase Chain Reaction MeSH Polymorphism (Genetics)* MeSH Polymorphism, Single-Stranded Conformational MeSH Receptors, Glucocorticoid/genetics* MeSH Regression Analysis MeSH Sex Characteristics MeSH Support, Non-U.S. Govt //

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