|
|
| ID |
243 |
| OMIM_ID |
603903
|
| Disease |
SICKLE CELL ANEMIA |
| Gene |
HBB
|
| SNP_ID |
rs12290192
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/C
|
| Orientation |
fwd/T |
| Chr-Number |
11 |
| SNP
type |
M |
| Length |
1001 |
| 5'
Near Seq 30 bp |
acaacaagagcaaaactccatctaaaaaaa |
| 3'
Near Seq 30 bp |
aaaaaaatctactctctttgcaaattttaa |
| Fasta
Sequence |
GCATTTTTTT ATTTTTTAGT TTTTTAATTC ATGTGATGTC TATTCTTTTT TATTAttctt
caactttatt gaggtatcat tcacaaataa aaattgtata tatttaaggt gtacaacatg
atgttttaat atatgtatac cttgtgaaat gattaccaca atcaagctaa ttaacatacc
cattatctca catagttacc tttttcttgt ggtaaatgct tttaagatct actctcggcc
aggcccggtg gctcacgcct gtaatcccag ccctttgggt ggccgaggca ggcggatcag
cctgaccaac atggagaaac cccgtctcta ctaaaaatac aaaattagct gggcatggtg
tcgcatgcct gtaatcccag ctactcggga ggctgaggca ggagatttgc ttgaacccag
gaggcggagg ttgcagtgag ccaagatctt gccattgcac tccagcctgg acaacaagag
caaaactcca tctaaaaaaa
M
aaaaaaatct actctctttg caaattttaa atatacttac agtacaatta actacagtca
cgatgctgta cattagatat ctagaattta ttcatcccac ataactgaaa ttttataccc
tttgagtaat agtttcctga ttctcccacc cccaacccct ggaaaccata cctctactgt
ctgtttccat gagagtgact tttttatgtt tcacatatga gcaaggttgt gtagtatttg
tctttttgtg tcaggcttat ttttcttagt tttacatcct ccaggttcat caattctgcc
ataaatggca ggattttctt ctttttAATT TTTTTATTTT CCTATTTtta attttttgtt
tgttattgaa tcatctgtgt ttcttatata ttttggatat taaccaaaat atttaagaaa
tatttggttt gcaaatatgc catttcatgg ttcacctttc atttgttcat tgttttgttt
tttgtgtgga aattttttaG
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