SNP Browser for Human [Homo spaiens] Genetic Disorders

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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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