SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 314
OMIM_ID 107400
Disease ALPHA-1-ANTITRYPSIN DEFICIENCY
Gene

SERPINA1

SNP_ID

rs877082

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number 14
SNP type Y
Length 821
5' Near Seq 30 bp aaactgaggctcagagaggctactggtctc
3' Near Seq 30 bp cacaatgtcacacagctcataagtggcaaa
Fasta Sequence tgtgtgacct tcgtgaagtc gccaaacctc tctgagcccc agtCATTGCT AGTAAGACCT GCCTTTGAGT TGGTATGATG TTCAAGTTAG ATAACAAAAT GTTTATACCC ATTAGAACAG AGAATAAATA GAACTACATT TCTTGCACTT ATGAGCTTTC TGTGAATCAG ACATCCCTAT GAAGTACCTC CCCTGGCTGT TTCTCATTTA CTCACTGTAG CAGCACTGCG ATGTGTGAGT ATATCTGCTG TGCTCTTAAA CTCCAAATCt gaggaaactg aggctcagag aggctactgg tctc Y cacaatgtca cacagctcat aagtggcaaa gctggCTTGA TGGGCTACTT GTTCCTCTGA ACCATACCAC CTCACCACAC TCTCCCCTTC GAGGGTCACG CTAAACTTCT GCAGAGGTAA TTCCTCCTTA AACCAGAAGG GTTGCTGGTG GCCCACAGCT CACGCCTAGC ACACTTCATG AGAAAAACAC CCTGTGCCCA GTGTGGAGCA GGCATTGAGC TGAAGGTGGT GAGCAGAAGC TCATCCACCA GATGTTGACA CAGCCCGCAG CCTTGGGCGA CCCACAGGAC TCCTCTTATT TAACTGGCAT TTGGTAGGAG AACAGGGGCA GAGTCAAAGA CAAGTTGGCT TTCTGGAGAG CCCAGGGCAG GGAAGGAGGT GGCAGCGCTG AAGGCGGTCA CCTTAGACAC CATCGTTTTA CTTTGAAGAA TTGTCTGTCA CACACGAGTT GACAGTCAGG ATGGGAGAAA CCCATTCAAC TAGCATACCT CCCCAAGGAA TTCCTGGGGT CCCCTG
     

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