SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 329
OMIM_ID 107400
Disease ALPHA-1-ANTITRYPSIN DEFICIENCY
Gene

SERPINA1

SNP_ID

rs1540256

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number 14
SNP type Y
Length 814
5' Near Seq 30 bp cgctccgagcctgtttcctcatctgtcaaa
3' Near Seq 30 bp gggctctaacccactctgatctcccagggc
Fasta Sequence GCCTGAGGCT GGTCAAAATT GAACCTCCTC CTGCTCTGAG CAGCCTAGGG GGCAGACTAA GCAGAGGGCT GTGCAGACCC ACATAAAGAG CCTACTGTGT GCCAGGCACT TCACCCGAGG CACTTCACAA GCATGCTTGG GAATGAAACT TCCAACTCTT TGGGATGCAG GTGAAACAGT TCCTGGTTCA GAGAGGTGAA GCGGCCTGCC TGAGGCAGCA CAGCTCTTCT TTACAGATGT GCTTCCCCAC CTCTACCCTG TCTCACGGCC CCCCATGCCA GCCTGACGGT TGTGTCTGCC TCAGTCATGC TCCATTTTTC CATCGGGACC ATCAAGAGGG TGTTTGTGTC TAAGGctgac tgggtaactt tggatgagcg gtctctccgc tccgagcctg tttcctcatc tgtcaaa Y gggCTCTAAC CCACTCTGAT CTCCCAGGGC GGCAGTAAGT CTTCAGCATC AGGCATTTTG GGGTGACTCA GTAAATGGTA GATCTTGCTA CCAGTGGAAC AGCCACTAAG GATTCTGCAG TGAGAGCAGA GGGCCAGCTA AGTGGTACTC TCCCAGAGAC TGTCTGACTC ACGCCACCCC CTCCACCTTG GACACAGGAC GCTGTGGTTT CTGAGCCAGG TACAATGACT CCTTTCGGTA AGTGCAGTGG AAGCTGTACA CTGCCCAGGC AAAGCGTCCG GGCAGCGTAG GCGGGCGACT CAGATCCCAG CCAGTGGACT TAGCCCCTGT TTGCTCCTCC GATAACTGGG GTGACCTTGG TTAATATTCA CCAGCAGCCT CCCCCGTTGC CCCTCT
     

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