|
|
| ID |
255 |
| OMIM_ID |
603903
|
| Disease |
SICKLE CELL ANEMIA |
| Gene |
HBB
|
| SNP_ID |
rs7110263
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
G/T
|
| Orientation |
fwd/B |
| Chr-Number |
11 |
| SNP
type |
K |
| Length |
601 |
| 5'
Near Seq 30 bp |
aatccttttctgagggatgaataaggcata |
| 3'
Near Seq 30 bp |
gcatcaggggctgttgccaatgtgcattag |
| Fasta
Sequence |
TTTCCTTCTT CAAGTAGACC TCTATAAGAC AACAGAGACA ACTAAGGCTG AGTGGCCAGG
CGAGGAGAAA CCATCTCGCC GTAAAACATG GAAGGAACAC TTCAGGGGAA AGGTGGTATC
TCTAAGCAAG AGAACTGAGT GGAGTCAAGG CTGAGAGATG CAGGATAAGC AAATGGGTAG
TGAAAAGACA TTCATGAGGA CAGCTAAAAC AATAAGTAAT GTAAAATACA GCATAGCAAA
ACTTTAACCT CCAAATCAAG CCTCTACTTG AATCCTTTTC TGAGGGATGA ATAAGGCATA
K
GCATCAGGGG CTGTTGCCAA TGTGCATTAG CTGTTTGCAG CCTCACCTTC TTTCATGGAG
TTTAAGATAT AGTGTATTTT CCCAAGGTTT GAACTAGCTC TTCATTTCTT TATGTTTTAA
ATGCACTGAC CTCCCACATT CCCTTTTTAG TAAAATATTC AGAAATAATT TAAATACATC
ATTGCAATGA AAATAAATGT TTTTTATTAG GCAGAATCCA GATGCTCAAG GCCCTTCATA
ATATCCCCCA GTTTAGTAGT TGGACTTAGG GAACAAAGGA ACCTTTAATA GAAATTGGAC
|
|
|