|
|
| 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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