|
|
| ID |
323 |
| OMIM_ID |
107400
|
| Disease |
ALPHA-1-ANTITRYPSIN DEFICIENCY |
| Gene |
SERPINA1
|
| SNP_ID |
rs1243165
|
| 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 |
tgtgcccaccccaaggctgccctcctgggg |
| 3'
Near Seq 30 bp |
ccccagaactgcctgatcgtgccgtggccc |
| Fasta
Sequence |
TGCCTGCATG TGACTGTAAA TCCCTCCCAT GTTTTCTCTG AGTCTCCCTT TGCCTGCTGA
GGCTGTATGT GGGCTCCAGG TAACAGTGCT GTCTTCGGGC CCCCTGAACT GTGTTCATGG
AGCATCTGGC TGGGTAGGCA CATGCTGGGC TTGAATCCAG GGGGGACTGA ATCCTCAGCT
TACGGACCTG GGCCCATCTG TTTCTGGAGG GCTCCAGTCT TCCTTGTCCT GTCTTGGAGT
CCCCAAGAAG GAATCACAGG GGAGGAACCA GATACCAGCC ATGACCCCAG GCTCCACCAA
GCATCTTCAT GTCCCCCTGC TCATCCCCCA CTCCCCCCCA CCCAGAGTTG CTCATCCTGC
CAGGGCTGGC TGTGCCCACC CCAAGGCTGC CCTCCTGGGG
R
CCCCAGAACT GCCTGATCGT GCCGTGGCCC AGTTTTGTGG CATCTGCAGC AACACAAGAG
AGAGGACAAT GTCCTCCTCT TGACCCGCTG TCACCTAACC AGACTCGGGC CCTGCACCTC
TCAGGCACTT CTGGAAAATG ACTGAGGCAG ATTCTTCCTG AAGCCCATTC TCCATGGGGC
AACAAGGACA CCTATTCTGT CCTTGTCCTT CCATCGCTGC CCCAGAAAGC CTCACATATC
TCCGTTTAGA ATCAGGTCCC TTCTCCCCAG ATGAAGAGGA GGGTCTCTGC TTTGTTTTCT
CTATCTCCTC CTCAGACTTG ACCAGGCCCA GCAGGCCCCA GAAGACCATT ACCCTATATC
CCTTCTCCTC CCTAGTCACA TGGCCATAGG CCTGCTGATG
|
|
|
