|
|
| ID |
260 |
| OMIM_ID |
300624
|
| Disease |
FRAGILE X MENTAL RETARDATION SYNDROME |
| Gene |
FMR1
|
| SNP_ID |
rs1805420
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/G
|
| Orientation |
fwd/B |
| Chr-Number |
X |
| SNP
type |
S |
| Length |
511 |
| 5'
Near Seq 30 bp |
ttcataccccttatcacagctgcaactact |
| 3'
Near Seq 30 bp |
atttacttgtctgacaatttgatttatgtc |
| Fasta
Sequence |
TTGCTATGGC CTTGAGGAAT GTGGCCCTAG ATCCACCGCT TTAAAGCTGG AGTTCCACCA
GCAGCAACAT CCTCTCATTC TGGGGCACCT GCCTGGGGCA GGTCATCCTG CCTCTGCCAA
CTCAGTGCTA TTAGTTAACT CTCACCTGCC ATATTCCAGC TGGAATCATC TCCCCTTCTC
CACCCCAGAC TAGGTCATGT TCCGCCATCA TGGAAGCGCC TATTCTTCAT ACCCCTTATC
ACAGCTGCAA CTACT
S
ATTTACTTGT CTGACAATTT GATTTATGTC CACCTACTTT GCTAGGTACT AAGTTCAATG
CTGGCAGTCG TTTCTTCTTT TTTTTTcttt tctgttttgc tcaccgattt ctcgttagca
cttagcacag tgtctggcac acgatagatg ctccgtcaac ttctcagttg gatACCAGCA
TCCCGAAGGG AACATGGATT AAGGCAGCTA TAAGCACGGT GTAAAAACAG GAATAAGAAA
AAGTTGAGGT TTGTT
|
|
|
