|
|
| ID |
262 |
| OMIM_ID |
300624
|
| Disease |
FRAGILE X MENTAL RETARDATION SYNDROME |
| Gene |
FMR1
|
| SNP_ID |
rs25724
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
G/T
|
| Orientation |
fwd/B |
| Chr-Number |
X |
| SNP
type |
K |
| Length |
801 |
| 5'
Near Seq 30 bp |
atgtctatgaagtaaaaaaaaaaaattgat |
| 3'
Near Seq 30 bp |
taaacgtctcagtaataaaataaatgagag |
| Fasta
Sequence |
GATGTTTTTA AAATCTTATT AAAGTTTCAA AAATCTGAAG ATTGTTTATC TAGATGTAAA
TTTTTATTAA AAAGTTGCAC TTATGAAAAA GCAAAAAATT AGTCTGACAG ATGTTTGCTC
CTGGTTTTAA ATTTCTACAT TTGACAAAAA CTAATGATAT GTGGGGGGAA AGTTGTGCAA
AGTAAATGTA TGTTGCAAAT AATCTTTTAT GAGCCCTTAA AAGGCAAAAA CGAAGACACT
TGAAAATAAT TCTCCATATT CCCAGACATA AAATTTCAAC ACATTTATTA CATAGGGTGC
CACTAAACCA TATTAAACAT ATACTCCTAT TTGTGCACAC ATGAACATAC CCTGCCCTTT
GGAAAAAAGT ATGTCTATGA AGTAAAAAAA AAAAATTGAT
K
TAAACGTCTC AGTAATAAAA TAAATGAGAG GTTTGTAGGT AGAATGTGCC TGGGAATTGA
CTACTGTAAT CACTTCAAGG AACTCTGGCA CAGCCTACCC GCCTAAAAGG TACAAATGGA
GAGGTGACAG TGTCAGTGTT CTACCCAGGG TTAGAATCCA AAATGATGCT AGACAGCCTC
CTCTGCATTG ATGAGTTTTT TTCCCCAGAA AAATAACTAT TTTCTGCTTT TCTTGTTTTT
CATTCTGATG CTTTTGTGGT TCTTTGCTAC CCATTCTGTC TAACTGGGCA TCATTAGTGG
TGGGTAGGCT GAAACCATAC TCAAGTAACT TGTTTGGATT TTCCTTGTTT CACAGTAGTT
TTCAGCACTA CACATGAACA GCCTGTTGGA GGCAGCCAGC
|
|
|
