|
|
| ID |
SNP6.129 |
| OMIM_ID |
203450
|
| Disease |
Alexander disease |
| Gene |
GFAP
|
| SNP_ID |
rs1126642
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
chromosome 17 |
| SNP
type |
R |
| Length |
201 |
| 5'
Near Seq 30 bp |
taccggcgccagttgcagtccttgacctgc |
| 3'
Near Seq 30 bp |
acctggagtctctgcgcggcacgaacgagt |
| Fasta
Sequence |
>gnl|dbSNP|rs1126642|allelePos=101|totalLen=201|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=129
TGCAGACCTG ACAGACGCTG CTGCCCGCAA CGCGGAGCTG CTCCGCCAGG CCAAGCACGA
AGCCAACGAC TACCGGCGCC AGTTGCAG
TCCTTGACCT GC
R
ACCTGGAGTC TC
TGCGCGGCAC GGTGAGCGCG GCCAGGGCAG GACGGGGACG GGCGGAGCAG GGACGGCCAC
CCCAGGAGAT GCCAGGGGAG AAGGGCCA
|
|
|
