SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 313
OMIM_ID 107400
Disease ALPHA-1-ANTITRYPSIN DEFICIENCY
Gene

SERPINA1

SNP_ID

rs877083

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 cctctgaaccataccacctcaccacactct
3' Near Seq 30 bp cccttcgagggtcacgctaaacttctgcag
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 tctctcacaa tgtcacacag ctcataagtg gcaaagctgg CTTGATGGGC TACTTGTTCC TCTGAACCAT ACCACCTCAC CACACTCT Y CCCTTCGAGG GTCACGCTAA ACTTCTGCAG AGGTAATTCC TCCTTAAACC AGAAGGGTTG CTGGTGGCCC ACAGCTCACG CCTAGCACAC TTCATGAGAA AAACACCCTG TGCCCAGTGT GGAGCAGGCA TTGAGCTGAA GGTGGTGAGC AGAAGCTCAT CCACCAGATG TTGACACAGC CCGCAGCCTT GGGCGACCCA CAGGACTCCT CTTATTTAAC TGGCATTTGG TAGGAGAACA GGGGCAGAGT CAAAGACAAG TTGGCTTTCT GGAGAGCCCA GGGCAGGGAA GGAGGTGGCA GCGCTGAAGG CGGTCACCTT AGACACCATC GTTTTACTTT GAAGAATTGT CTGTCACACA CGAGTTGACA GTCAGGATGG GAGAAACCCA TTCAACTAGC ATACCTCCCC AAGGAATTCC TGGGGTCCCC TG
     

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