|
|
| ID |
253 |
| OMIM_ID |
603903
|
| Disease |
SICKLE CELL ANEMIA |
| Gene |
HBB
|
| SNP_ID |
rs10837630
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/G
|
| Orientation |
fwd/B |
| Chr-Number |
11 |
| SNP
type |
S |
| Length |
601 |
| 5'
Near Seq 30 bp |
acagtagtgaatatcaagctacaaaaagcc |
| 3'
Near Seq 30 bp |
cctttcaaattcttctcagtcctaactttt |
| Fasta
Sequence |
CAGAATTTGA CTGGGAGAGA GGACAAGGAC CACTTGAGAC TCATATTTTA TTTCCAGAAT
CTAGCATCTA CCTACCTAGG TATTGAATAA GAAAAATGAA GTTAAGGTGG TTGATGGTAA
CACTATGCTA ATAACTGCAG AGCCAGAAGC ACCATAAGGG ACATGATAAG GGAGCCAGCA
GACCTCTGAT CTCTTCCTGA ATGCTAATCT TAAACATCCT GAGGAAGAAT GGGACTTCCA
TTTGGGGTGG GCCTATGACA GGGTAATAAG ACAGTAGTGA ATATCAAGCT ACAAAAAGCC
S
CCTTTCAAAT TCTTCTCAGT CCTAACTTTT CATACTAAGC CCAGTCCTTC CAAAGCAGAC
TGTGAAAGAG TGATAGTTCC GGGAGACTAG CACTGCAGAT TCCGGGTCAC TGTGAGTGGG
GGAGGCAGGG AAGAAGGGCT CACAGGACAG TCAAACCATG ACCCCTGTTT TTCCTTCTTC
AAGTAGACCT CTATAAGACA ACAGAGACAA CTAAGGCTGA GTGGCCAGGC GAGGAGAAAC
CATCTCGCCG TAAAACATGG AAGGAACACT TCAGGGGAAA GGTGGTATCT CTAAGCAAGA
|
|
|
