|
|
| ID |
73 |
| OMIM_ID |
143100
|
| Disease |
HUNTINGTON DISEASE |
| Gene |
HTT
|
| SNP_ID |
rs28616835
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
4 |
| SNP
type |
Y |
| Length |
701 |
| 5'
Near Seq 30 bp |
ggcctgcgcccgcgctcggcgccccctcca |
| 3'
Near Seq 30 bp |
ggccccgccccgtccatggccccgtccttc |
| Fasta
Sequence |
TCCCCGTGCA GAGAGCCCCG CAGCTGGCTC CCCGCAGGGC TGTCCGGGTG AGTATGGCTC
TGGCCACGGG CCAGTGTGGC GGGAGGGCAA ACCCCAAGGC CACCTCGGCT CAGAGTCCAC
GGCCGGCTGT CGCCCCGCTC CAGGCGTCGG CGGGGGATCC TTTCCGCATG GGCCTGCGCC
CGCGCTCGGC GCCCCCTCCA
R
GGCCCCGCCC CGTCCATGGC CCCGTCCTTC ATGGGCGAGC CCCTCCATGG CCCTGCCCCT
CCGCGCCCCA CCCCTCCCTC GCCCCACCTC TCACCTTCCT GCCCCGCCCC CAGCCTCCCC
AACCCTCACC GGCCAGTCCC CTCCCCTATC CCGTCCGCCC CTCAGCCGCC CCGCCCCTCA
GCCGGCCTGC CTAATGTCCC CGTCCCCAGC ATCGCCCCGC CCCGCCCCCG TCTCGCCCCG
CCCCTCAGGC GGCCTCCCTG CTGTGCCCCG CCCCGGCCTC GCCACGCCCC TACCTCACCA
CGCCCCCCGC ATCGCCACGC CCCCCGCATC GCCACGCCTC CCTTACCATG CAGTCCCGCC
CCGTCCCTTC CTCGTCCCGC CTCGCCGCGA CACTTCACAC ACAGCTTCGC CTCACCCCAT
TACAGTCTCA CCACGCCCCG TCCCCTCTCC GTTGAGCCCC GCGCCTTCGC CCGGGTGGGG
CGCTGCGCTG TCAGCGGCCT
|
|
|
