|
|
| ID |
315 |
| OMIM_ID |
107400
|
| Disease |
ALPHA-1-ANTITRYPSIN DEFICIENCY |
| Gene |
SERPINA1
|
| SNP_ID |
rs877081
|
| 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 |
cagagaataaatagaactacatttcttgca |
| 3'
Near Seq 30 bp |
ttatgagctttctgtgaatcagacatccct |
| Fasta
Sequence |
tgtgtgacct tcgtgaagtc gccaaacctc tctgagcccc agtCATTGCT AGTAAGACCT
GCCTTTGAGT TGGTATGATG TTCAAGTTAG ATAACAAAAT GTTTATACCC ATTAGAACAG
AGAATAAATA GAACTACATT TCTTGCA
Y
TTATGAGCTT TCTGTGAATC AGACATCCCT ATGAAGTACC TCCCCTGGCT GTTTCTCATT
TACTCACTGT AGCAGCACTG CGATGTGTGA GTATATCTGC TGTGCTCTTA AACTCCAAAT
Ctgaggaaac tgaggctcag agaggctact ggtctctcac aatgtcacac agctcataag
tggcaaagct ggCTTGATGG GCTACTTGTT CCTCTGAACC ATACCACCTC ACCACACTCT
CCCCTTCGAG GGTCACGCTA AACTTCTGCA GAGGTAATTC CTCCTTAAAC CAGAAGGGTT
GCTGGTGGCC CACAGCTCAC GCCTAGCACA CTTCATGAGA AAAACACCCT GTGCCCAGTG
TGGAGCAGGC ATTGAGCTGA AGGTGGTGAG CAGAAGCTCA TCCACCAGAT GTTGACACAG
CCCGCAGCCT TGGGCGACCC ACAGGACTCC TCTTATTTAA CTGGCATTTG GTAGGAGAAC
AGGGGCAGAG TCAAAGACAA GTTGGCTTTC TGGAGAGCCC AGGGCAGGGA AGGAGGTGGC
AGCGCTGAAG GCGGTCACCT TAGACACCAT CGTTTTACTT TGAAGAATTG TCTGTCACAC
ACGAGTTGAC AGTCAGGATG GGAGAAACCC ATTCAACTAG CATACCTCCC CAAGGAATTC
CTGGGGTCCC CTG
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