|
|
| ID |
309 |
| OMIM_ID |
100800
|
| Disease |
Achondroplasia |
| Gene |
FGFR3
|
| SNP_ID |
rs10023340
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
4 |
| SNP
type |
Y |
| Length |
616 |
| 5'
Near Seq 30 bp |
cccctctaacgagctgccttcctcctcctg |
| 3'
Near Seq 30 bp |
agtctcccgagcggcgcccgcctcccgccg |
| Fasta
Sequence |
GGGCAGGCTC GCGGAGGGGT CCAACGGTGC TCGCGGAGGG GTCGGGGCGC GGCTGTCGCG
GAACCACAGA GGTCCCTGCA gcgggccggg ccggggcgcg ggcTTCCCGC TCCGGAAAGT
TTGCCGCCGC CGCCGCCCTG GGAGGGCTTT GCAGCAGCca gggagggaag ggggaggagg
gagggaccgc ggcggggagg aggcggccgg cgccaggcgg cccgggagcc ctgggcggcg
gcggcggcgg gcggggcggc tgggggtcgg aggggtcggg acgCAGGAGC CGGCCACCGC
CGCTTTCGTC CCTGTCCGCC CCTCTAACGA GCTGCCTTCC TCCTCCTG
Y
AGTCTCCCGA gcggcgcccg cctcccgccg gtgcccgcgc cgggccgtgg ggggcAGCAT
GCCCGCGCGC GCTGCCTGAG GAcgccgcgg cccccgcccc cgccATGGGC GCCCCTGCCT
GCGCCCTCGC GCTCTGCGTG GCCGTGGCCA TCGTGGCCGG CGCCTCCTCG GAGTCCTTGG
GGACGGAGCA GCGCGTCGTG GGGCGAGCGG CAGGTAAGAA GGGACCCACT AGGCACGGGA
GAGGCCGGCC CGTGCGGGCA GAGGCGT
|
|
|
