Identification of Two Single Nucleotide Polymorphisms in Exon 8 of PAX2

We estimate the allele frequencies of two single nucleotide polymorphisms (1410 C → T) and (1521 A → C) in the coding region of PAX2. The coding region single nucleotide polymorphisms (cSNPs) were identified by sequencing of amplimers of PAX2 exon 8 exhibiting variant migration patterns in the cours...

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Veröffentlicht in:Molecular genetics and metabolism 1999-12, Vol.68 (4), p.507-510
Hauptverfasser: Shim, Heather H, Nakamura, Brooke N, Cantor, Rita M, Schimmenti, Lisa A
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Sprache:eng
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Zusammenfassung:We estimate the allele frequencies of two single nucleotide polymorphisms (1410 C → T) and (1521 A → C) in the coding region of PAX2. The coding region single nucleotide polymorphisms (cSNPs) were identified by sequencing of amplimers of PAX2 exon 8 exhibiting variant migration patterns in the course of genomic DNA mutation screening from patients with renal-coloboma syndrome. Allele frequencies of the two polymorphisms were 0.94 for 1410C and 0.72 for 1521A. Cosegregation analyses of both alleles suggest that they are each in Hardy-Weinberg equilibrium and jointly in linkage equilibrium and may represent ancient polymorphisms. Characterization of PAX2 exon 8 cSNPs will serve as useful tools for mapping at the PAX2 locus.
ISSN:1096-7192
1096-7206
DOI:10.1006/mgme.1999.2931