|
|
| ID |
SNP6.094 |
| OMIM_ID |
203450
|
| Disease |
Alexander disease |
| Gene |
GFAP
|
| SNP_ID |
rs11558961
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/G
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome 17 |
| SNP
type |
S |
| Length |
601 |
| 5'
Near Seq 30 bp |
tgaggcaggacccacctggtggcctctgcc |
| 3'
Near Seq 30 bp |
cgtctcatgaggggcccgagcagaagcagg |
| Fasta
Sequence |
>gnl|dbSNP|rs11558961|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/G'|mol=Genomic|build=126
GCTCATCTTA CTCCAGCAGC TTACCACTCG CCAGGCATGA CGCTAAATGC TTTCCCAGTG
TTATCTCACC ACCCCCTCTG TCCACCACGC AAGGCAGCTG TGGTTACTAT CAAGAAAAGT
AAGACCTGGG AAGTCGGGGA CTTCCCAAGG TTACACAGCC TCGTGGTGGT GGACCTGGGG
TCTGTGTGAA CTCCTAACTG TTGCACTGTG CACGTTCCCT GTCCCCTGCA GGTCATTAAG
GAGTCCAAGC AGGAGCACAA GGATGTGATG TGAGGCAGGA CCCACCTGGT GGCCTCTGCC
S
CGTCTCATGA GGGGCCCGAG CAGAAGCAGG ATAGTTGCTC CGCCTCTGCT GGCACATTTC
CCCAGACCTG AGCTCCCCAC CACCCCAGCT GCTCCCCTCC CTCCTCTGTC CCTAGGTCAG
CTTGCTGCCC TAGGCTCCGT CAGTATCAGG CCTGCCAGAC GGCACCCACC CAGCACCCAG
CAACTCCAAC TAACAAGAAA CTCACCCCCA AGGGGCAGTC TGGAGGGGCA TGGCCAGCAG
CTTGCGTTAG AATGAGGAGG AAGGAGAGAA GGGGAGGAGG GCGGGGGGCA CCTACTACAT
|
|
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