|
|
| ID |
SNP6.135 |
| OMIM_ID |
203450
|
| Disease |
Alexander disease |
| Gene |
GFAP
|
| SNP_ID |
rs7049
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome 17 |
| SNP
type |
Y |
| Length |
197 |
| 5'
Near Seq 30 bp |
ccccaagacttggtgtcctttccctccact |
| 3'
Near Seq 30 bp |
cttcctgccacctgctgctgctgctgctgc |
| Fasta
Sequence |
>gnl|dbSNP|rs7049|allelePos=101|totalLen=197|taxid=9606|snpclass=1|alleles='C/T'|mol=cDNA|build=120
GATGGGACTG GGAGGGCCCA CTTCAGGGTT CTCCTCTCCC CTCTAAGGCC GAAGAAGGGT
CCTTCCCTCT CCCCAAGACT TGGTGTCCTT TCCCTCCACT
Y
CTTCCTGCCA Cctgctgctg ctgctgctgc tAATCTTCAG GGCACTGCTG CTGCCTTTAG
TCGCTGAGGA AAAATAAAGA CAAATGCTGC GCCCTT
|
|
|
