|
|
| ID |
SNP6.026 |
| OMIM_ID |
203450
|
| Disease |
Alexander disease |
| Gene |
GFAP
|
| SNP_ID |
rs60343255
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome 17 |
| SNP
type |
Y |
| Length |
201 |
| 5'
Near Seq 30 bp |
gctggcttcaaggagacccgggccagtgag |
| 3'
Near Seq 30 bp |
gggcagagatgatggagctcaatgaccgct |
| Fasta
Sequence |
>gnl|dbSNP|rs60343255|allelePos=101|totalLen=201|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=129
CCTCTCCCTG GCTCGAATGC CCCCTCCACT CCCGACCCGG GTGGATTTCT CCCTGGCTGG
GGCACTCAAT GCTGGCTTCA AGGAGACCCG GGCCAGTGAG
Y
GGGCAGAGAT GATGGAGCTC AATGACCGCT TTGCCAGCTA CATCGAGAAG GTTCGCTTCC
TGGAACAGCA AAACAAGGCG CTGGCTGCTG AGCTGAACCA
|
|
|