SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 315
OMIM_ID 107400
Disease ALPHA-1-ANTITRYPSIN DEFICIENCY
Gene

SERPINA1

SNP_ID

rs877081

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 cagagaataaatagaactacatttcttgca
3' Near Seq 30 bp ttatgagctttctgtgaatcagacatccct
Fasta Sequence tgtgtgacct tcgtgaagtc gccaaacctc tctgagcccc agtCATTGCT AGTAAGACCT GCCTTTGAGT TGGTATGATG TTCAAGTTAG ATAACAAAAT GTTTATACCC ATTAGAACAG AGAATAAATA GAACTACATT TCTTGCA Y TTATGAGCTT TCTGTGAATC AGACATCCCT ATGAAGTACC TCCCCTGGCT GTTTCTCATT TACTCACTGT AGCAGCACTG CGATGTGTGA GTATATCTGC TGTGCTCTTA AACTCCAAAT Ctgaggaaac tgaggctcag agaggctact ggtctctcac aatgtcacac agctcataag tggcaaagct ggCTTGATGG GCTACTTGTT CCTCTGAACC ATACCACCTC ACCACACTCT CCCCTTCGAG GGTCACGCTA AACTTCTGCA GAGGTAATTC CTCCTTAAAC CAGAAGGGTT GCTGGTGGCC CACAGCTCAC GCCTAGCACA CTTCATGAGA AAAACACCCT GTGCCCAGTG TGGAGCAGGC ATTGAGCTGA AGGTGGTGAG CAGAAGCTCA TCCACCAGAT GTTGACACAG CCCGCAGCCT TGGGCGACCC ACAGGACTCC TCTTATTTAA CTGGCATTTG GTAGGAGAAC AGGGGCAGAG TCAAAGACAA GTTGGCTTTC TGGAGAGCCC AGGGCAGGGA AGGAGGTGGC AGCGCTGAAG GCGGTCACCT TAGACACCAT CGTTTTACTT TGAAGAATTG TCTGTCACAC ACGAGTTGAC AGTCAGGATG GGAGAAACCC ATTCAACTAG CATACCTCCC CAAGGAATTC CTGGGGTCCC CTG
     

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