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|
| ID |
317 |
| OMIM_ID |
107400
|
| Disease |
ALPHA-1-ANTITRYPSIN DEFICIENCY |
| Gene |
SERPINA1
|
| SNP_ID |
rs9944155
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
14 |
| SNP
type |
Y |
| Length |
701 |
| 5'
Near Seq 30 bp |
ggtatgactcaacctcatcctttaagtaca |
| 3'
Near Seq 30 bp |
attcatgacagtgagtggttagacagtgat |
| Fasta
Sequence |
ATCGCAGTGC TGCTACAGTG AGTAAATGAG AAACAGCCAG GGGAGGTACT TCATAGGGAT
GTCTGATTCA CAGAAAGCTC ATAAGTGCAA GAAATGTAGT TCTATTTATT CTCTGTTCTA
ATGGGTATAA ACATTTTGTT ATCTAACTTG AACATCATAC CAACTCAAAG GCAGGTCTTA
CTAGCAATGa ctggggctca gagaggtttg gcgacttcac gaaggtcaca cagctgtcag
ggggaaaagt cagaacttgg atccaggtct tcagactctc agGTCTGGTG TCATCCTAGG
GGGCTTGGTG ATGGCCATAT CTTTAATGTA TTTGTGGAGA GTGAAAGGCT GTCAGTGAGT
AAGCTTAAGA GAACAGGAGA CTTGTGTGGG AAACAGTCGG TATCCATTGA TTAGACTGAA
TCATGTAGAA TTGCTAATTT CACCATTTTG AACTATCGAA ATCACTATTT GGTATGACTC
AACCTCATCC TTTAAGTACA
Y
ATTCATGACA GTGAGTGGTT AGACAGTGAT TCCTAGATTA GTTTGGGATG GGGCAGTGCC
TTCCATAGGA CAAGGCCATT CCTGGTAGAG ACGGAGGGAG CAGGCTGTCC TTCAGCTAGG
GGCCCAGGGG ACTTCCTGGC TGCTGTGTCC TTTAGCAGGG CCTTGGAGGA TGGAAGGACT
CTCCTGGCCC TTACCACAGG
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