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|
| ID |
314 |
| OMIM_ID |
107400
|
| Disease |
ALPHA-1-ANTITRYPSIN DEFICIENCY |
| Gene |
SERPINA1
|
| SNP_ID |
rs877082
|
| 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 |
aaactgaggctcagagaggctactggtctc |
| 3'
Near Seq 30 bp |
cacaatgtcacacagctcataagtggcaaa |
| Fasta
Sequence |
tgtgtgacct tcgtgaagtc gccaaacctc tctgagcccc agtCATTGCT AGTAAGACCT
GCCTTTGAGT TGGTATGATG TTCAAGTTAG ATAACAAAAT GTTTATACCC ATTAGAACAG
AGAATAAATA GAACTACATT TCTTGCACTT ATGAGCTTTC TGTGAATCAG ACATCCCTAT
GAAGTACCTC CCCTGGCTGT TTCTCATTTA CTCACTGTAG CAGCACTGCG ATGTGTGAGT
ATATCTGCTG TGCTCTTAAA CTCCAAATCt gaggaaactg aggctcagag aggctactgg
tctc
Y
cacaatgtca cacagctcat aagtggcaaa gctggCTTGA TGGGCTACTT GTTCCTCTGA
ACCATACCAC CTCACCACAC TCTCCCCTTC GAGGGTCACG CTAAACTTCT GCAGAGGTAA
TTCCTCCTTA AACCAGAAGG GTTGCTGGTG GCCCACAGCT CACGCCTAGC ACACTTCATG
AGAAAAACAC CCTGTGCCCA GTGTGGAGCA GGCATTGAGC TGAAGGTGGT GAGCAGAAGC
TCATCCACCA GATGTTGACA CAGCCCGCAG CCTTGGGCGA CCCACAGGAC TCCTCTTATT
TAACTGGCAT TTGGTAGGAG AACAGGGGCA GAGTCAAAGA CAAGTTGGCT TTCTGGAGAG
CCCAGGGCAG GGAAGGAGGT GGCAGCGCTG AAGGCGGTCA CCTTAGACAC CATCGTTTTA
CTTTGAAGAA TTGTCTGTCA CACACGAGTT GACAGTCAGG ATGGGAGAAA CCCATTCAAC
TAGCATACCT CCCCAAGGAA TTCCTGGGGT CCCCTG
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