|
|
| ID |
485 |
| OMIM_ID |
104300
|
| Disease |
Alzheimer disease |
| Gene |
APP
|
| SNP_ID |
rs11326732
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/T
|
| Orientation |
fwd/B |
| Chr-Number |
21 |
| SNP
type |
N |
| Length |
801 |
| 5'
Near Seq 30 bp |
agcaaccactctttattttcctactttctt |
| 3'
Near Seq 30 bp |
aaaacttcatttccttttcctctatggacc |
| Fasta
Sequence |
TGGGTAAAAT AAGGCTGGGA CCTACTGGGC TGCATTCCCA GAGGGTTAAG TCATTCTAAG
TCACAGGATG AGATTGTAGG TCTGCATAAG ATACAGGTCA TAAAGACCTT GCTCATAAAA
CAAGTTGCAG TAAAGAAGCC GGTCAAAACC CACCAAAACC AAGATAGCAA TGAGAGTGAC
CTCTGGTTGT CCTCACTGCT ACACTCCCAC TAGAGCCATG ACGGTTTACA AATGCCATGG
CAACATCAGG AAGTTACCCT ATATGGTCTA CCAAGGGGAG GCATGAATAA TTCAGCCCTT
GTTTAGTAAA TAATTAAGAA ATAACAATAA AATGGGCAAC CAGCAGCCCT TAGGTTCACT
CTGCCTATGG AGCAACCACT CTTTATTTTC CTACTTTCTT
N
AAAACTTCAT TTCCTTTTCC TCTATGGACC CGCCTTGAAT TCTTTCTTGC ATGAGATCCA
AGAACCCTGT CTTGGGGTCT GGATTGGGAC CCCTTTCTGG TAACAAAATG ATCAAAGTTA
AAGCTGTAGT TACTGTAACT GAGTTGGCCT TGGAATGCCA TCCCATATAG TGCCATGTTT
GAGAGCTGGT TTTCATTTCA TTGGTGGCAT TAGAAATGTA CTATTATATT AGGGTTAATT
CGCCCTGCTA CCCCAACTAG CTAGCTACCT CCCCTTGGGC CAGGCAAAAT GGAACAGTAG
CTTGTACATA TGAATTGTTA ACATGTACAT ATCTTCATAC AGCAGTCATG TCTAACTGTC
CCTAACAGGG CAAGGGAGAT GACCGGTCAT TTTTTCTCAT
|
|
|
