8,9 1|||||IVIII-8III-7III-3III-1III-51,2The pedigree above shows the pattern of inheritance of a vision disorder calledLeber congenital amaurosis, which is due to mutations in a gene on chromosome19 (filled symbols show affected individuals). Identification of the gene hingedon mapping it to a precise chromosomal location. Results of a small part of thatmapping effort are shown above, analyzing linkage between a SNP marker onchr. 19 and the vision disorder in this family. The numbers below each person'spedigree symbol show what alleles they have for this SNP marker.Which individual in generation III has inherited a recombinant chromosome?III-22,21,2 2,21 2 3 45 6(71,2 2,2 2,2 1,2 2,2 1,2 1,281,2 2,2?1,2 SNP A SNP BResults of ASO (antisense oligonucleotide) genotyping for two SNP markers areshown here for individual III-1 in the pedigree provided for Question 8. Orangeindicates the presence of a hybridization signal and white indicates nohybridization. Which of these markers could be the one informing the SNPgenotype designation "1,2" for individual III-1?SNP ACould be eitherSNP B

Name: 8,9 1|||||IVIII-8III-7III-3III-1III-51,2The pedigree above shows the p
Uploaded: 2024-03-20T06:42:55.000Z
Channel: Bartleby
Description: 8,9 1|||||IVIII-8III-7III-3III-1III-51,2The pedigree above shows the pattern of inheritance of a vision disorder calledLeber congenital amaurosis, which is due to mutations in a gene on chromosome19 (filled symbols show affected individuals). Identif