|
|
| ID |
SNP6.133 |
| OMIM_ID |
203450
|
| Disease |
Alexander disease |
| Gene |
GFAP
|
| SNP_ID |
rs17027
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/C/G/T
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome 17 |
| SNP
type |
N |
| Length |
601 |
| 5'
Near Seq 30 bp |
gagaaccctgaagtgggccctcccagtccc |
| 3'
Near Seq 30 bp |
tctctgggcacagatcccaccagtctgctc |
| Fasta
Sequence |
>gnl|dbSNP|rs17027|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='A/C/G/T'|mol=Genomic|build=126
TGGGCCCCAG AGATGATCAG TAATAAGAAA TGAGTTGGTC TTGTCAAAGG CTACATCTTG
GCCCCAGTCC CGCCCTCTCA TGAACAGATC AGAGTCCACT CTGGGGAAGG GCGCAGCATT
TGTCTTTATT TTTCCTCAGC GACTAAAGGC AGCAGCAGTG CCCTGAAGAT TAGCAGCAGC
AGCAGCAGCA GGTGGCAGGA AGGAGTGGAG GGAAAGGACA CCAAGTCTTG GGGAGAGGGA
AGGACCCTTC TTCGGCCTTA GAGGGGAGAG GAGAACCCTG AAGTGGGCCC TCCCAGTCCC
N
TCTCTGGGCA CAGATCCCAC CAGTCTGCTC ACCAGTCTGC TCAGTCAAAG CAGAGTGGGT
GCACTGGGGT GGACGTGTCA GCCCTGAGCA CCCGGCCTCC AGGCTGCAGG AATATGAGCC
AGTGTCTTCA CTTTGCTCGT GCCTCAGTTT TACAATTGTA AAATAGGGCA CTACCTAGAA
TACTGGGTAC ATTTTGTGTG TGAGTAAGAA GGGACCGCAA GAGGCCCTTG GCTTAGGGAA
AAGCAGCCGG TCACTATGGG GTGGAGAGGG TCAGACGTGT GGCAGTGGCT TACTGGGGTT
|
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