SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 320
OMIM_ID 107400
Disease ALPHA-1-ANTITRYPSIN DEFICIENCY
Gene

SERPINA1

SNP_ID

rs1243166

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 attgacccccgcaacccctccctttcctcc
3' Near Seq 30 bp ctgagtcccgactggggccacatgcagcct
Fasta Sequence GACACCTATT CTGTCCTTGT CCTTCCATCG CTGCCCCAGA AAGCCTCACA TATCTCCGTT TAGAATCAGG TCCCTTCTCC CCAGATGAAG AGGAGGGTCT CTGCTTTGTT TTCTCTATCT CCTCCTCAGA CTTGACCAGG CCCAGCAGGC CCCAGAAGAC CATTACCCTA TATCCCTTCT CCTCCCCAGT CACATGGCCA TAGGCCTGCT GATGGCTCAG GAAGGCCATT GCAAGGACTC CTCAGCTATG GGAGAGGAAG CACATCACCC ATTGACCCCC GCAACCCCTC CCTTTCCTCC Y CTGAGTCCCG ACTGGGGCCA CATGCAGCCT GACTTCTTTG TGCCTGTTGC TGTCCCTGCA GTCTTCAGAG GGCCACCGCA GCTCCAGTGC CACGGCAGGA GGCTGTTCCT GAATAGCCCC TGTGGTAAGG GCCAGGAGAG TCCTTCCATC CTCCAAGGCC CTGCTAAAGG ACACAGCAGC CAGGAAGTCC CCTGGGCCCC TAGCTGAAGG ACAGCCTGCT CCCTCCGTCT CTACCAGGAA TGGCCTTGTC CTATGGAAGG CACTGCCCCA TCCCAAACTA ATCTAGGAAT CACTGTCTAA
     

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