|
|
| ID |
263 |
| OMIM_ID |
300624
|
| Disease |
FRAGILE X MENTAL RETARDATION SYNDROME |
| Gene |
FMR1
|
| SNP_ID |
rs25703
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
X |
| SNP
type |
Y |
| Length |
401 |
| 5'
Near Seq 30 bp |
gaggtttgtaggtagaatgtgcctgggaat |
| 3'
Near Seq 30 bp |
gactactgtaatcacttcaaggaactctgg |
| Fasta
Sequence |
TTCCCAGACA TAAAATTTCA ACACATTTAT TACATAGGGT GCCACTAAAC CATATTAAAC
ATATACTCCT ATTTGTGCAC ACATGAACAT ACCCTGCCCT TTGGAAAAAA GTATGTCTAT
GAAGTAAAAA AAAAAAATTG ATTTAAACGT CTCAGTAATA AAATAAATGA GAGGTTTGTA
GGTAGAATGT GCCTGGGAAT
Y
GACTACTGTA ATCACTTCAA GGAACTCTGG CACAGCCTAC CCGCCTAAAA GGTACAAATG
GAGAGGTGAC AGTGTCAGTG TTCTACCCAG GGTTAGAATC CAAAATGATG CTAGACAGCC
TCCTCTGCAT TGATGAGTTT TTTTCCCCAG AAAAATAACT ATTTTCTGCT TTTCTTGTTT
TTCATTCTGA TGCTTTTGTG
|
|
|
