|
|
| ID |
386 |
| OMIM_ID |
173900
|
| Disease |
POLYCYSTIC KIDNEY DISEASE |
| Gene |
PKD1
|
| SNP_ID |
rs35688748
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/A
|
| Orientation |
fwd/ |
| Chr-Number |
16 |
| SNP
type |
N |
| Length |
601 |
| 5'
Near Seq 30 bp |
tgtctacaatgactccggtgaggacttcaa |
| 3'
Near Seq 30 bp |
gcttggcaccatcaaggtgagtgaggggcc |
| Fasta
Sequence |
CTTTGCGTCC CAAAGCCCTG CCCCTGGGGA GAGCCGAGGA CCACTGGCCA GGCACCAGAG
GACGTGGTCC CCGCAGGCCC CCAGAGCCCC TGGAGTAATC AGGAGGTGCC CCAGTGCAAG
GCACAGAGGG CCTCAGCACT GGCCCCACAA ACCCATCCGG CCCTGCTCAC CCTCAGCCGT
CTTCCACATC GCCACCCTGA TGCCCACCAA GGACGTGGAC AAGCACCGCT GCGACAAGAA
GCGCCACCTG GGCAACGACT TTGTGTCCAT TGTCTACAAT GACTCCGGTG AGGACTTCAA
N
GCTTGGCACC ATCAAGGTGA GTGAGGGGCC GTCAGTGAGG CTGGGCCCCA GGCAGGTGCC
CACTGCTGTG TCCCGGGTTG GTGGCAGGTC CTCCTCCCTG AGCTTCGGTC ACGAGGAGCA
GGAGGAGAGG CCGCAGTGCT CAGGGCCCCG TGGGCACGAG CTTCACCCCG AGCCTGCGTT
GTGTCCTCTG TGCCCTGAAG CCTGTGGCGC CTGCTGCTGA GTGTCTGTCA GGAGTAACTG
GCAAGTGCAG ACTGGGTGTG CTGGGTGGGC ACAGTGTAGT TGGTGCTTCC TGTCTGTCCG
|
|
|
