|
|
| ID |
391 |
| OMIM_ID |
173900
|
| Disease |
POLYCYSTIC KIDNEY DISEASE |
| Gene |
PKD1
|
| SNP_ID |
rs36032671
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/AA
|
| Orientation |
fwd/ |
| Chr-Number |
16 |
| SNP
type |
N |
| Length |
601 |
| 5'
Near Seq 30 bp |
ggacggtattgcctgtcagtgaaataaata |
| 3'
Near Seq 30 bp |
gtcctgaccccagtgcacagacatagaggc |
| Fasta
Sequence |
GCTGTGGGGC GGGTGTGTGG GCAGAGCGGT TGCCACGCCT CCCAGACTTA CTGCCCAAGC
CGCCTCTGCC TTCAGATCTG CGAGGAAGCC GCCTACTCCA ACCCCAGCCT ACCTCTGGTG
CACCCTCCGT CCCATAGCAA AGCCCCTGCA CAGACTCCAG CCGAGCCCAC ACCTGGCTAT
GAGGTGGGCC AGCGGAAGCG CCTCATCTCC TCGGTGGAGG ACTTCACCGA GTTTGTGTGA
GGCCGGGGCC CTCCCTCCTG CACTGGCCTT GGACGGTATT GCCTGTCAGT GAAATAAATA
N
GTCCTGACCC CAGTGCACAG ACATAGAGGC ACAGATTGCA GTCAGACAGC TCTTTTATTG
ACTTTGTCTG CTTGGTGCGG GGGTTGGGGG GGTGTCGAGG CTCTAGAAGC GGCCATGCCC
ACAGAAGTGG TACACAGAAG CAGGCACAGC CAGCTCCGAG GGCCTTGAGG CTGCCTGGGC
CATACAGCAC ACTCGCGCGT GCGCGCGCGC ACACACACAC ACACACAGTC ACCTTCCTCC
ACCCTGGGAG CCAGCCCCCA GGAGGAGTCT TTTCCTCTAA CCACCCTGGG GTCCTCTGAC
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