SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 327
OMIM_ID 107400
Disease ALPHA-1-ANTITRYPSIN DEFICIENCY
Gene

SERPINA1

SNP_ID

rs2073333

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/G
Orientation fwd/T
Chr-Number 14
SNP type R
Length 601
5' Near Seq 30 bp ttcatggagcatctggctgggtaggcacat
3' Near Seq 30 bp ctgggcttgaatccaggggggactgaatcc
Fasta Sequence TTGTCTTCTT AATGATTGAA CAAAATACCA AGTCTCCCCT CTTCATGGGA AAAGTGGTGA ATCCCACCCA AAAATAACTG CCTCTCGCTC CTCAACCCCT CCCCTCCATC CCTGGCCCCC TCCCTGGATG ACATTAAAGA AGGGTTGAGC TGGTCCCTGC CTGCATGTGA CTGTAAATCC CTCCCATGTT TTCTCTGAGT CTCCCTTTGC CTGCTGAGGC TGTATGTGGG CTCCAGGTAA CAGTGCTGTC TTCGGGCCCC CTGAACTGTG TTCATGGAGC ATCTGGCTGG GTAGGCACAT R CTGGGCTTGA ATCCAGGGGG GACTGAATCC TCAGCTTACG GACCTGGGCC CATCTGTTTC TGGAGGGCTC CAGTCTTCCT TGTCCTGTCT TGGAGTCCCC AAGAAGGAAT CACAGGGGAG GAACCAGATA CCAGCCATGA CCCCAGGCTC CACCAAGCAT CTTCATGTCC CCCTGCTCAT CCCCCACTCC CCCCCACCCA GAGTTGCTCA TCCTGCCAGG GCTGGCTGTG CCCACCCCAA GGCTGCCCTC CTGGGGGCCC CAGAACTGCC TGATCGTGCC GTGGCCCAGT TTTGTGGCAT
     

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