|
|
| ID |
397 |
| OMIM_ID |
173900
|
| Disease |
POLYCYSTIC KIDNEY DISEASE |
| Gene |
PKD1
|
| SNP_ID |
rs241569
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/T
|
| Orientation |
fwd/B |
| Chr-Number |
16 |
| SNP
type |
W |
| Length |
992 |
| 5'
Near Seq 30 bp |
cctcggccgactctgcagtgcgacgggcgg |
| 3'
Near Seq 30 bp |
gcttccagacgctccgccccacgtcgcatg |
| Fasta
Sequence |
CTCATTTAAT AAAGGGAATA ATTGTAGCAC ACTTTTTCTA GAGCTGTGAA GATTCAATGG
AATAAATAAG GCAATAAATG AATGGATGGG GAATGAAGGA TGTGGGTTTC CTCCCTCTTG
TCTTTCAATA AGCTCTCACC ATCAACCTCC CATTGCCTGT tctctctctt ccccctctct
ccctctgtct ctctctcAGC CAGGAAACCT GGGGTAGGGA GGCTTGGAGC CAGCGGGTGC
GTCGGGAGGC TGCGGGTACT GACTCGGGCC GCGCACGGAG ATCGCGGGAG AAGGATCCAC
AACCGCGGAA GAAGGATCAG GGTGGAGCCT GTGGCTGCTG CAGGAGGAGG AACCCGCCGC
CTGGCCCACA CCACAGGAGA AGGGCGGAGC AGATGGCACC CTGCCCACCG CTTCCCGCCC
ACGCACTTTA GCCTGCAGCG GGGCGGAGCG TGAAAAATAG CTCGTGCTCC TCGGCCGACT
CTGCAGTGCG ACGGCGG
W
GCTTCCAGAC GCTCCGCCCC ACGTCGCATG CGCCCCGGGA ACGCGTGGGG CGGAGCTTCC
GGAGGCCCCG CCCTGCTGCC GACCCTGTGG AGCGGAGGGT GAAGCCTCCG GATGCCAGTC
CCTCATCGCT GGCCCGGTCG CGCTGTGGCG AAGGGGGCGG AGCCTGCAcc cgccccgccc
cccctcgccc cgtccgcccc gcgccgcGCG GGGAGGAGGA GGAGGAGCCG CGGCGGGGCC
CGCACTGCAG CGCCAGCGTC CGAGCGGGCG GCCGAGCTCC CGGAGCGGCC TGGCCCCGAG
CCCCGAGCGG GCGTCGCTCA GCAGCAGGTC GCGGCCGCAG CCCCATCCAG CCCGCGCCCG
CCATGCCGTC CGCGGGCCCC GCCTGAGCTG CGGCCTCCGC GCGCGGGCGG GCCTGGGGAC
GGCGGGGCCA TGCGCGCGCT GCCCTAACGA Tgccgcccgc cgcgcccgcc cgccTGGCGC
TGGCCCTGGG CCTG
|
|
|
