SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 399
OMIM_ID 173900
Disease POLYCYSTIC KIDNEY DISEASE
Gene

PKD1

SNP_ID

rs154653

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number 16
SNP type Y
Length 701
5' Near Seq 30 bp cgggtactgactcgggccgcgcacggagat
3' Near Seq 30 bp gcgggagaaggatccacaaccgcggaagaa
Fasta Sequence cctcagcctc tcgagtacct gggactacaa gcgtgagcca gtttggctaa ttttggctaa tttttgtaga aacggggtct cgccatgttg gccaggctgg tctccaactc ctggactcaa gggatccacc ttcctccccc tctcaaagtt ctgggattac cggagtgagc cactgtgccc tgctggcaaa tttcttaaac tgtctgtgcc tcagtgacct catttaataa agggaataat tgtagcacac tttttctaga gctgtgaaga ttcaatggaa taaataAGGC AATAAATGAA TGGATGGGGA ATGAAGGATG TGGGTTTCCT CCCTCTTGTC TTTCAATAAG CTCTCACCAT CAACCTCCCA TTGCCTGTtc tctctcttcc ccctctctcc ctctgtctct ctctcAGCCA GGAAACCTGG GGTAGGGAGG CTTGGAGCCA GCGGGTGCGT CGGGAGGCTG CGGGTACTGA CTCGGGCCGC GCACGGAGAT Y GCGGGAGAAG GATCCACACC GCGGAAGAAG GATCAGGGTG GAGCCTGTGG CTGCTGCAGG AGGAGGAACC CGCCGCCTGG CCCACACCAC AGGAGAAGGG CGGAGCCAGA TGGCACCCTG CCCACCGCTT CCCGCCCACG CACTTTAGCC TGCAGCGGGG CGGAGCGTGA AAAATAGCTC GTGCGCCTCG GCCGACTCTG
     

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