|
|
| ID |
68 |
| OMIM_ID |
143100
|
| Disease |
HUNTINGTON DISEASE |
| Gene |
HTT
|
| SNP_ID |
rs9996199
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/G
|
| Orientation |
fwd/T |
| Chr-Number |
4 |
| SNP
type |
S |
| Length |
701 |
| 5'
Near Seq 30 bp |
gcaggtgtggcctggctaaagtaggcttta |
| 3'
Near Seq 30 bp |
tgggctcctctctgcctgcatcaccccccg |
| Fasta
Sequence |
ctgcctcagc ctccggaata gctgggacta caggcatgca ccactacacc cggctaattt
ttgtattttt agtagagaca gggtttcgcc atgttggcca ggctggtctc gaactcctga
cctctggtga tctgcctgcc ttggcctccc aaagtgctgg gattacaggc gtgagccacc
gcaccTCGCT GGAACTTAAt ttttttagag acagtgtcgc tctatcaccc aagctggagt
gcagtggtgc aatcctagct cacttgcagc ctcaaattcc tgggttcagg tgatcctccc
acatcagcct cccaagaact gggaACTAAC GGCTGTTTCT CTGCTGTCCT TCTCAAGAAA
AGGGAGGCTA CTGCTACCCC ACTGGGGACA ATGCTGGGTT TCCCTTTAGG ACAGGCTCTG
AGACAAGGCG GAGGTGCTGT TTGTGGCCAC AGAGCAGGGG ACTCTGGGTT GCAGGTGTGG
CCTGGCTAAA GTAGGCTTTA
S
TGGGCTCCTC TCTGCCTGCA TCACCCCCCG GCTGGGCGGT TGTCTCTGAG GCCAACCTTA
CTCCCTGCTG GGCAGGCTGG ACAGCTGCCC TCTCCGTTTG CCCCTCTACC ACCCAAAAGG
CAGGAGGCTC TGGAGACCAG GACCCTGCCC GCCACGGCCT GTGTCCCAGG CGTGAGGGGG
TGCCCCACAG ACCTCTGCTG
|
|
|
