|
|
| ID |
102 |
| OMIM_ID |
143100
|
| Disease |
HUNTINGTON DISEASE |
| Gene |
HTT
|
| SNP_ID |
rs396875
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
4 |
| SNP
type |
R |
| Length |
401 |
| 5'
Near Seq 30 bp |
aggcggggccgcgccggcggaggcggggcc |
| 3'
Near Seq 30 bp |
cgccggccagcatgattgacagccctagcc |
| Fasta
Sequence |
CCGGCACGGC AGTCCCCGGA GGCCTCGGGC CGACTCGCGG CGCCGCTCAG CACCGGGGCA
ATGAATGGGG CTCTGGGCCG CAGGTAAAAG CAGAACCTGA GCGGCCGTCC ATCTTGGACC
CGTCCCGGCA GCCCCCACGG CGCCTTGCGT CCCAGACGCT gcgccggcgg aggcggggcc
gcgccggcgg aggcggggcc
R
cgccggccAG CATGATTGAC AGCCCTAGCC TGCGGACTCT GCCAATGGCT GGCCAGGGAA
CCAGCCCGCC CCTGCCCCCG CAGGTTCTGC CTCACACAGC AAGGCCGCTG ACAGCGCAGC
GCCCCACCCG GGCGAAGGCG CGGGGCTCAA CGGAGAGGGG ACGGGGCGTG GTGAGACTGT
AATGGGGTGA GGCGAATCTG
|
|
|
