SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 321
OMIM_ID 107400
Disease ALPHA-1-ANTITRYPSIN DEFICIENCY
Gene

SERPINA1

SNP_ID

rs1051052

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 agaccattaccctatatcccttctcctccc
3' Near Seq 30 bp agtcacatggccataggctgnctgatggct
Fasta Sequence CCTCCTCTTG ACCCGCTGTC ACCTAACCAG ACTCGGGCCC TGCACCTCTC AGGCACTTCT GGAAAATGAC TGAGGCAGAT TCTTCCTGAA GCCCATTCTC CATGGGGCAA CAAGGACACC TATTCTGTCC TTGTCCTTCC ATCGCTGCCC CAGAAAGCCT CACATATCTC CGTTTAGAAT CAGGTCCCTT CTCCCCAGAT GAAGAGGAGG GTCTCTGCTT TGTTTTCTCT ATCTCCTCCT CAGACTTGAC CAGGCCCAGC AGGCCCCAGA AGACCATTAC CCTATATCCC TTCTCCTCCC Y AGTCACATGG CCATAGGCCT GCTGATGGCT CAGGAAGGCC ATTGCAAGGA CTCCTCAGCT ATGGGAGAGG AAGCACATCA CCCATTGACC CCCGCAACCC CTCCCTTTCC TCCTCTGAGT CCCGACTGGG GCCACATGCA GCCTGACTTC TTTGTGCCTG TTGCTGTCCC TGCAGTCTTC AGAGGGCCAC CGCAGCTCCA GTGCCACGGC AGGAGGCTGT TCCTGAATAG CCCCTGTGGT AAGGGCCAGG AGAGTCCTTC CATCCTCCAA GGCCCTGCTA AAGGACACAG CAGCCAGGAA
     

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