SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 317
OMIM_ID 107400
Disease ALPHA-1-ANTITRYPSIN DEFICIENCY
Gene

SERPINA1

SNP_ID

rs9944155

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number 14
SNP type Y
Length 701
5' Near Seq 30 bp ggtatgactcaacctcatcctttaagtaca
3' Near Seq 30 bp attcatgacagtgagtggttagacagtgat
Fasta Sequence ATCGCAGTGC TGCTACAGTG AGTAAATGAG AAACAGCCAG GGGAGGTACT TCATAGGGAT GTCTGATTCA CAGAAAGCTC ATAAGTGCAA GAAATGTAGT TCTATTTATT CTCTGTTCTA ATGGGTATAA ACATTTTGTT ATCTAACTTG AACATCATAC CAACTCAAAG GCAGGTCTTA CTAGCAATGa ctggggctca gagaggtttg gcgacttcac gaaggtcaca cagctgtcag ggggaaaagt cagaacttgg atccaggtct tcagactctc agGTCTGGTG TCATCCTAGG GGGCTTGGTG ATGGCCATAT CTTTAATGTA TTTGTGGAGA GTGAAAGGCT GTCAGTGAGT AAGCTTAAGA GAACAGGAGA CTTGTGTGGG AAACAGTCGG TATCCATTGA TTAGACTGAA TCATGTAGAA TTGCTAATTT CACCATTTTG AACTATCGAA ATCACTATTT GGTATGACTC AACCTCATCC TTTAAGTACA Y ATTCATGACA GTGAGTGGTT AGACAGTGAT TCCTAGATTA GTTTGGGATG GGGCAGTGCC TTCCATAGGA CAAGGCCATT CCTGGTAGAG ACGGAGGGAG CAGGCTGTCC TTCAGCTAGG GGCCCAGGGG ACTTCCTGGC TGCTGTGTCC TTTAGCAGGG CCTTGGAGGA TGGAAGGACT CTCCTGGCCC TTACCACAGG
     

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