SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 319
OMIM_ID 107400
Disease ALPHA-1-ANTITRYPSIN DEFICIENCY
Gene

SERPINA1

SNP_ID

rs11628917

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number 14
SNP type Y
Length 601
5' Near Seq 30 bp cttaccacaggggctattcaggaacagcct
3' Near Seq 30 bp ctgccgtggcactggagctgcggtggccct
Fasta Sequence TCATGTAGAA TTGCTAATTT CACCATTTTG AACTATCGAA ATCACTATTT GGTATGACTC AACCTCATCC TTTAAGTACA CATTCATGAC AGTGAGTGGT TAGACAGTGA TTCCTAGATT AGTTTGGGAT GGGGCAGTGC CTTCCATAGG ACAAGGCCAT TCCTGGTAGA GACGGAGGGA GCAGGCTGTC CTTCAGCTAG GGGCCCAGGG GACTTCCTGG CTGCTGTGTC CTTTAGCAGG GCCTTGGAGG ATGGAAGGAC TCTCCTGGCC CTTACCACAG GGGCTATTCA GGAACAGCCT Y CTGCCGTGGC ACTGGAGCTG CGGTGGCCCT CTGAAGACTG CAGGGACAGC AACAGGCACA AAGAAGTCAG GCTGCATGTG GCCCCAGTCG GGACTCAGAG GAGGAAAGGG AGGGGTTGCG GGGGTCAATG GGTGATGTGC TTCCTCTCCC ATAGCTGAGG AGTCCTTGCA ATGGCCTTCC TGAGCCATCA GCAGGCCTAT GGCCATGTGA CTGGGGAGGA GAAGGGATAT AGGGTAATGG TCTTCTGGGG CCTGCTGGGC CTGGTCAAGT CTGAGGAGGA GATAGAGAAA ACAAAGCAGA
     

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