| ID |
261 |
| OMIM_ID |
300624
|
| Disease |
FRAGILE X MENTAL RETARDATION SYNDROME |
| Gene |
FMR1
|
| SNP_ID |
rs28902
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/G
|
| Orientation |
fwd/B |
| Chr-Number |
X |
| SNP
type |
S |
| Length |
278 |
| 5'
Near Seq 30 bp |
cgctcagtcagactgcgctactttgaaccg |
| 3'
Near Seq 30 bp |
accaaaccaaaccaaaccaaaccaaaccaa |
| Fasta
Sequence |
CTGGTGAGAG AGGGCGTAGA CGCCTCACCT TCTGCCTCTA CGGGTCACAA AAGCCTGGGT
CACCCTGGTT GCCACTGTTC CTAGTTCAAA GTCTTCTTCT GTCTAATCCT TCACCCCTAT
TCTCGCCTTC CACTCCACCT CCCGCTCAGT CAGACTGCGC TACTTTGaac cg
S
accaaaccaa accaaaccaa accaaaccaa accagaccag acACCCCCTC CCGCGGAATC
CCAGAGAGGC CGAACTGGGA TAACCGGATG CATTTGATTT CCCAC
|
