|
|
| ID |
322 |
| OMIM_ID |
107400
|
| Disease |
ALPHA-1-ANTITRYPSIN DEFICIENCY |
| Gene |
SERPINA1
|
| SNP_ID |
rs45538932
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
14 |
| SNP
type |
R |
| Length |
801 |
| 5'
Near Seq 30 bp |
gcagggcccgagtctggttaggtgacagcg |
| 3'
Near Seq 30 bp |
gtcaagaggaggacattgtcctctctcttg |
| Fasta
Sequence |
GAGGAAAGGG AGGGGTTGCG GGGGTCAATG GGTGATGTGC TTCCTCTCCC ATAGCTGAGG
AGTCCTTGCA ATGGCCTTCC TGAGCCATCA GCAGGCCTAT GGCCATGTGA CTAGGGAGGA
GAAGGGATAT AGGGTAATGG TCTTCTGGGG CCTGCTGGGC CTGGTCAAGT CTGAGGAGGA
GATAGAGAAA ACAAAGCAGA GACCCTCCTC TTCATCTGGG GAGAAGGGAC CTGATTCTAA
ACGGAGATAT GTGAGGCTTT CTGGGGCAGC GATGGAAGGA CAAGGACAGA ATAGGTGTCC
TTGTTGCCCC ATGGAGAATG GGCTTCAGGA AGAATCTGCC TCAGTCATTT TCCAGAAGTG
CCTGAGAGGT GCAGGGCCCG AGTCTGGTTA GGTGACAGCG
R
GTCAAGAGGA GGACATTGTC CTCTCTCTTG TGTTGCTGCA GATGCCACAA AACTGGGCCA
CGGCACGATC AGGCAGTTCT GGGGCCCCCA GGAGGGCAGC CTTGGGGTGG GCACAGCCAG
CCCTGGCAGG ATGAGCAACT CTGGGTGGGG GGGAGTGGGG GATGAGCAGG GGGACATGAA
GATGCTTGGT GGAGCCTGGG GTCATGGCTG GTATCTGGTT CCTCCCCTGT GATTCCTTCT
TGGGGACTCC AAGACAGGAC AAGGAAGACT GGAGCCCTCC AGAAACAGAT GGGCCCAGGT
CCGTAAGCTG AGGATTCAGT CCCCCCTGGA TTCAAGCCCA GCATGTGCCT ACCCAGCCAG
ATGCTCCATG AACACAGTTC AGGGGGCCCG AAGACAGCAC
|
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