|
|
| ID |
326 |
| OMIM_ID |
107400
|
| Disease |
ALPHA-1-ANTITRYPSIN DEFICIENCY |
| Gene |
SERPINA1
|
| SNP_ID |
rs1243164
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
G/T
|
| Orientation |
fwd/B |
| Chr-Number |
14 |
| SNP
type |
K |
| Length |
801 |
| 5'
Near Seq 30 bp |
ggagggctccagtcttccttgtcctgtctt |
| 3'
Near Seq 30 bp |
gagtccccaagaaggaatcacaggggagga |
| Fasta
Sequence |
CAAACCCTTT GTCTTCTTAA TGATTGAACA AAATACCAAG TCTCCCCTCT TCATGGGAAA
AGTGGTGAAT CCCACCCAAA AATAACTGCC TCTCGCTCCT CAACCCCTCC CCTCCATCCC
TGGCCCCCTC CCTGGATGAC ATTAAAGAAG GGTTGAGCTG GTCCCTGCCT GCATGTGACT
GTAAATCCCT CCCATGTTTT CTCTGAGTCT CCCTTTGCCT GCTGAGGCTG TATGTGGGCT
CCAGGTAACA GTGCTGTCTT CGGGCCCCCT GAACTGTGTT CATGGAGCAT CTGGCTGGGT
AGGCACATGC TGGGCTTGAA TCCAGGGGGG ACTGAATCCT CAGCTTACGG ACCTGGGCCC
ATCTGTTTCT GGAGGGCTCC AGTCTTCCTT GTCCTGTCTT
K
GAGTCCCCAA GAAGGAATCA CAGGGGAGGA ACCAGATACC AGCCATGACC CCAGGCTCCA
CCAAGCATCT TCATGTCCCC CTGCTCATCC CCCACTCCCC CCCACCCAGA GTTGCTCATC
CTGCCAGGGC TGGCTGTGCC CACCCCAAGG CTGCCCTCCT GGGGGCCCCA GAACTGCCTG
ATCGTGCCGT GGCCCAGTTT TGTGGCATCT GCAGCAACAC AAGAGAGAGG ACAATGTCCT
CCTCTTGACC CGCTGTCACC TAACCAGACT CGGGCCCTGC ACCTCTCAGG CACTTCTGGA
AAATGACTGA GGCAGATTCT TCCTGAAGCC CATTCTCCAT GGGGCAACAA GGACACCTAT
TCTGTCCTTG TCCTTCCATC GCTGCCCCAG AAAGCCTCAC
|
|
|
