|
|
| ID |
313 |
| OMIM_ID |
107400
|
| Disease |
ALPHA-1-ANTITRYPSIN DEFICIENCY |
| Gene |
SERPINA1
|
| SNP_ID |
rs877083
|
| 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 |
cctctgaaccataccacctcaccacactct |
| 3'
Near Seq 30 bp |
cccttcgagggtcacgctaaacttctgcag |
| 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
tctctcacaa tgtcacacag ctcataagtg gcaaagctgg CTTGATGGGC TACTTGTTCC
TCTGAACCAT ACCACCTCAC CACACTCT
Y
CCCTTCGAGG GTCACGCTAA ACTTCTGCAG AGGTAATTCC TCCTTAAACC AGAAGGGTTG
CTGGTGGCCC ACAGCTCACG CCTAGCACAC TTCATGAGAA AAACACCCTG TGCCCAGTGT
GGAGCAGGCA TTGAGCTGAA GGTGGTGAGC AGAAGCTCAT CCACCAGATG TTGACACAGC
CCGCAGCCTT GGGCGACCCA CAGGACTCCT CTTATTTAAC TGGCATTTGG TAGGAGAACA
GGGGCAGAGT CAAAGACAAG TTGGCTTTCT GGAGAGCCCA GGGCAGGGAA GGAGGTGGCA
GCGCTGAAGG CGGTCACCTT AGACACCATC GTTTTACTTT GAAGAATTGT CTGTCACACA
CGAGTTGACA GTCAGGATGG GAGAAACCCA TTCAACTAGC ATACCTCCCC AAGGAATTCC
TGGGGTCCCC TG
|
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