|
|
| ID |
256 |
| OMIM_ID |
603903
|
| Disease |
SICKLE CELL ANEMIA |
| Gene |
HBB
|
| SNP_ID |
rs12574989
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
11 |
| SNP
type |
Y |
| Length |
601 |
| 5'
Near Seq 30 bp |
tccttttctgagggatgaataaggcatatg |
| 3'
Near Seq 30 bp |
atcaggggctgttgccaatgtgcattagct |
| Fasta
Sequence |
TCCTTCTTCA AGTAGACCTC TATAAGACAA CAGAGACAAC TAAGGCTGAG TGGCCAGGCG
AGGAGAAACC ATCTCGCCGT AAAACATGGA AGGAACACTT CAGGGGAAAG GTGGTATCTC
TAAGCAAGAG AACTGAGTGG AGTCAAGGCT GAGAGATGCA GGATAAGCAA ATGGGTAGTG
AAAAGACATT CATGAGGACA GCTAAAACAA TAAGTAATGT AAAATACAGC ATAGCAAAAC
TTTAACCTCC AAATCAAGCC TCTACTTGAA TCCTTTTCTG AGGGATGAAT AAGGCATATG
Y
ATCAGGGGCT GTTGCCAATG TGCATTAGCT GTTTGCAGCC TCACCTTCTT TCATGGAGTT
TAAGATATAG TGTATTTTCC CAAGGTTTGA ACTAGCTCTT CATTTCTTTA TGTTTTAAAT
GCACTGACCT CCCACATTCC CTTTTTAGTA AAATATTCAG AAATAATTTA AATACATCAT
TGCAATGAAA ATAAATGTTT TTTATTAGGC AGAATCCAGA TGCTCAAGGC CCTTCATAAT
ATCCCCCAGT TTAGTAGTTG GACTTAGGGA ACAAAGGAAC CTTTAATAGA AATTGGACAG
|
|
|
