SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 312
OMIM_ID 107400
Disease ALPHA-1-ANTITRYPSIN DEFICIENCY
Gene

SERPINA1

SNP_ID

rs877084

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/T
Orientation fwd/T
Chr-Number 14
SNP type W
Length 821
5' Near Seq 30 bp cttaaaccagaagggttgctggtggcccac
3' Near Seq 30 bp gctcacgcctagcacacttcatgagaaaaa
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 CACACTCTCC CCTTCGAGGG TCACGCTAAA CTTCTGCAGA GGTAATTCCT CCTTAAACCA GAAGGGTTGC TGGTGGCCCA C W GCTCACGCCT AGCACACTTC ATGAGAAAAA CACCCTGTGC CCAGTGTGGA GCAGGCATTG AGCTGAAGGT GGTGAGCAGA AGCTCATCCA CCAGATGTTG ACACAGCCCG CAGCCTTGGG CGACCCACAG GACTCCTCTT ATTTAACTGG CATTTGGTAG GAGAACAGGG GCAGAGTCAA AGACAAGTTG GCTTTCTGGA GAGCCCAGGG CAGGGAAGGA GGTGGCAGCG CTGAAGGCGG TCACCTTAGA CACCATCGTT TTACTTTGAA GAATTGTCTG TCACACACGA GTTGACAGTC AGGATGGGAG AAACCCATTC AACTAGCATA CCTCCCCAAG GAATTCCTGG GGTCCCCTG
     

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