|
|
| ID |
329 |
| OMIM_ID |
107400
|
| Disease |
ALPHA-1-ANTITRYPSIN DEFICIENCY |
| Gene |
SERPINA1
|
| SNP_ID |
rs1540256
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
14 |
| SNP
type |
Y |
| Length |
814 |
| 5'
Near Seq 30 bp |
cgctccgagcctgtttcctcatctgtcaaa |
| 3'
Near Seq 30 bp |
gggctctaacccactctgatctcccagggc |
| Fasta
Sequence |
GCCTGAGGCT GGTCAAAATT GAACCTCCTC CTGCTCTGAG CAGCCTAGGG GGCAGACTAA
GCAGAGGGCT GTGCAGACCC ACATAAAGAG CCTACTGTGT GCCAGGCACT TCACCCGAGG
CACTTCACAA GCATGCTTGG GAATGAAACT TCCAACTCTT TGGGATGCAG GTGAAACAGT
TCCTGGTTCA GAGAGGTGAA GCGGCCTGCC TGAGGCAGCA CAGCTCTTCT TTACAGATGT
GCTTCCCCAC CTCTACCCTG TCTCACGGCC CCCCATGCCA GCCTGACGGT TGTGTCTGCC
TCAGTCATGC TCCATTTTTC CATCGGGACC ATCAAGAGGG TGTTTGTGTC TAAGGctgac
tgggtaactt tggatgagcg gtctctccgc tccgagcctg tttcctcatc tgtcaaa
Y
gggCTCTAAC CCACTCTGAT CTCCCAGGGC GGCAGTAAGT CTTCAGCATC AGGCATTTTG
GGGTGACTCA GTAAATGGTA GATCTTGCTA CCAGTGGAAC AGCCACTAAG GATTCTGCAG
TGAGAGCAGA GGGCCAGCTA AGTGGTACTC TCCCAGAGAC TGTCTGACTC ACGCCACCCC
CTCCACCTTG GACACAGGAC GCTGTGGTTT CTGAGCCAGG TACAATGACT CCTTTCGGTA
AGTGCAGTGG AAGCTGTACA CTGCCCAGGC AAAGCGTCCG GGCAGCGTAG GCGGGCGACT
CAGATCCCAG CCAGTGGACT TAGCCCCTGT TTGCTCCTCC GATAACTGGG GTGACCTTGG
TTAATATTCA CCAGCAGCCT CCCCCGTTGC CCCTCT
|
|
|