|
|
| ID |
312 |
| OMIM_ID |
107400
|
| Disease |
ALPHA-1-ANTITRYPSIN DEFICIENCY |
| Gene |
SERPINA1
|
| SNP_ID |
rs877084
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/T
|
| Orientation |
fwd/T |
| Chr-Number |
14 |
| SNP
type |
W |
| Length |
821 |
| 5'
Near Seq 30 bp |
cttaaaccagaagggttgctggtggcccac |
| 3'
Near Seq 30 bp |
gctcacgcctagcacacttcatgagaaaaa |
| 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 CACACTCTCC CCTTCGAGGG TCACGCTAAA CTTCTGCAGA
GGTAATTCCT CCTTAAACCA GAAGGGTTGC TGGTGGCCCA C
W
GCTCACGCCT AGCACACTTC ATGAGAAAAA CACCCTGTGC CCAGTGTGGA GCAGGCATTG
AGCTGAAGGT GGTGAGCAGA AGCTCATCCA CCAGATGTTG ACACAGCCCG CAGCCTTGGG
CGACCCACAG GACTCCTCTT ATTTAACTGG CATTTGGTAG GAGAACAGGG GCAGAGTCAA
AGACAAGTTG GCTTTCTGGA GAGCCCAGGG CAGGGAAGGA GGTGGCAGCG CTGAAGGCGG
TCACCTTAGA CACCATCGTT TTACTTTGAA GAATTGTCTG TCACACACGA GTTGACAGTC
AGGATGGGAG AAACCCATTC AACTAGCATA CCTCCCCAAG GAATTCCTGG GGTCCCCTG
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