|
|
| ID |
318 |
| OMIM_ID |
107400
|
| Disease |
ALPHA-1-ANTITRYPSIN DEFICIENCY |
| Gene |
SERPINA1
|
| SNP_ID |
rs11832
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
14 |
| SNP
type |
R |
| Length |
601 |
| 5'
Near Seq 30 bp |
gattagtttgggatggggcagtgccttcca |
| 3'
Near Seq 30 bp |
aggacaaggccattcctggtagagacggag |
| Fasta
Sequence |
GAGGAAGCAC ATCACCCATT GACCCCCGCA ACCCCTCCCT TTCCTCCTCT GAGTCCCGAC
TGGGGCCACA TGCAGCCTGA CTTCTTTGTG CCTGTTGCTG TCCCTGCAGT CTTCAGAGGG
CCACCGCAGC TCCAGTGCCA CGGCAGGAGG CTGTTCCTGA ATAGCCCCTG TGGTAAGGGC
CAGGAGAGTC CTTCCATCCT CCAAGGCCCT GCTAAAGGAC ACAGCAGCCA GGAAGTCCCC
TGGGCCCCTA GCTGAAGGAC AGCCTGCTCC CTCCGTCTCT ACCAGGAATG GCCTTGTCCT
R
TGGAAGGCAC TGCCCCATCC CAAACTAATC TAGGAATCAC TGTCTAACCA CTCACTGTCA
TGAATGTGTA CTTAAAGGAT GAGGTTGAGT CATACCAAAT AGTGATTTCG ATAGTTCAAA
ATGGTGAAAT TAGCAATTCT ACATGATTCA GTCTAATCAA TGGATACCGA CTGTTTCCCA
CACAAGTCTC CTGTTCTCTT AAGCTTACTC ACTGACAGCC TTTCACTCTC CACAAATACA
TTAAAGATAT GGCCATCACC AAGCCCCCTA GGATGACACC AGACCTGAGA GTCTGAAGAC
|
|
|
