|
|
| ID |
267 |
| OMIM_ID |
231000
|
| Disease |
GAUCHER DISEASE |
| Gene |
GBA
|
| SNP_ID |
rs368793
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
1 |
| SNP
type |
Y |
| Length |
401 |
| 5'
Near Seq 30 bp |
gtgggcttctgacctccatgctctcctgag |
| 3'
Near Seq 30 bp |
ctctgtgtgggtctgtgtgttcccgtcccc |
| Fasta
Sequence |
GCTGCATGCG GCCAGGCAGG AAGAAGTTGA GGGGAAAGGG CATAGCCTCT GCATACCACT
TCCGGGTCAC TTCTACGTAG TTCTTGGTGT CTATCCAAAA AGTATGTACC TGGATTGGGT
GGGCAGGAAG AAACAGGCAG GTCTGAGCCA GTGCACCTGT CTGATTCAAG GTGGGCTTCT
GACCTCCATG CTCTCCTGAG
Y
CTCTGTGTGG GTCTGTGTGT TCCCGTCCCC TCCCCGGCTG GCCATGGATG CTGGGAGGTC
TGGGCACACT CACCAGCACC GGGATCAACT TCTCCTCCAG GAGAGACATG AAGGCCAGGG
TGTCTGCCCC TTGCTGAGCT GACAGATCAT AATCAGCATT GTACTTCTGT GGAGGAAATA
TCCATGGCGT GGACGCTGGG
|
|
|
