|
|
| ID |
71 |
| OMIM_ID |
143100
|
| Disease |
HUNTINGTON DISEASE |
| Gene |
HTT
|
| SNP_ID |
rs2857935
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/G
|
| Orientation |
fwd/T |
| Chr-Number |
4 |
| SNP
type |
S |
| Length |
401 |
| 5'
Near Seq 30 bp |
agcgcgggcgcaggcccatgcggaaaggat |
| 3'
Near Seq 30 bp |
ccccgccgacgcctggagcggggcgacaac |
| Fasta
Sequence |
AGCGGGATAG gggaggggac tggccggtga ggggtgggga ggctgggggc ggggcaggaa
ggtgagaggt ggggcgaggg aggggtgggg cgcggagggg cagggccatg gaggggctcg
cccatgaagg acggggccat ggacggggcg gggccgtgga gggggcgccg agcgcgggcg
CAGGCCCATG CGGAAAGGAT
S
CCCCGCCGAC GCCTGGAGCG GGGCGACAAC CGGCCGTGGA CTCTGAGCCG AGGTGGCCTT
GGGGTTTGCC CTCCCGCCAC ACTGGCCCGT GGCCAGAGCC ATACTCACCC GGACAGCCCT
GCGGGGAGCC AGCTGCGGGG CTCTCTGCAC GGGGAGAGGG TGGGCGAGCT CCTGCGCAGA
GCGCAGAGAA TGCGCGTGGT
|
|
|
