|
|
| ID |
259 |
| OMIM_ID |
300624
|
| Disease |
FRAGILE X MENTAL RETARDATION SYNDROME |
| Gene |
FMR1
|
| SNP_ID |
rs35739145
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
X |
| SNP
type |
Y |
| Length |
201 |
| 5'
Near Seq 30 bp |
atgtaaacaaggaccctgtagggactgata |
| 3'
Near Seq 30 bp |
gacaatgtgctgaaaattgaggagcaaagt |
| Fasta
Sequence |
CTTGTGTCTA GAAGAATGAG AGTGGGGATC GAGAAAGATG AGGAAAAAAT AATATAAACA
CTATAAAATA ATGTAAACAA GGACCC
TGTAGGGACT GATA
Y
GACAATGTGC TGAA
AATTGAGGAG CAAAGTTAAC TCTCTGTACC TGAGATAAAA TAACTAGCTA ATAGGAATCC
AGCTGAAAAC CTTAAGGTGC AGGGCC
|
|
|
