|
|
| ID |
SNP6.134 |
| OMIM_ID |
203450
|
| Disease |
Alexander disease |
| Gene |
GFAP
|
| SNP_ID |
rs12222
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome 17 |
| SNP
type |
Y |
| Length |
601 |
| 5'
Near Seq 30 bp |
tttcaacactgatcagtgtttacca |
| 3'
Near Seq 30 bp |
tggataaatctgagttcacactttccttct |
| Fasta
Sequence |
>gnl|dbSNP|rs12222|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=129
GAGGAAAAAT AAAGACAAAT GCTGCGCCCT TCCCCAGAGT GGACTCTGAT CTGTTCATGA
GAGGGCGGGA CTGGGGCCAA GATGTAGCCT TTGACAAGAC CAACTCATTT CTTATTACTG
ATCATCTCTG GGGCCCATGC CCTCACCAAA TTCCACCCGC AGCCAAAGAG GACATACACC
AGCTCCCTCC ACTCTTTTCT TCCTTCCTCT CCCTGCTACC TGCAACTCAA CCAGCACAAT
CTTCATAGGC AAGAAAGCAA AGCAGCTCAA ACATGATTCA ACACTGATCA GTGTTTACCA
Y
TGGATAAATC TGAGTTCACA CTTTCCTTCT CTGACCTAAA TGTGAAGTCA GGAAACACAT
GTGCCCTACT TCCATCCTGA GCTCAGTCCC CAATCTCCCA CCAGCCTCAG GCCCCTCCAC
TTCTCAGATC AGGTCCCAGA CCTGCCCATG AAAATGGGGA GCAGGCTGTA ACAGATTTGT
CCACATGTTC CTACCACCTG TCCCAACCCA GGGTACCCAC CCAGAGACAT CTGGTATCAT
TTAACAAACA CATTGAAGGA CAACTGGTCT TCAGAGCTGA AGAGAGCTCC TAGGGGGAGA
|
|
|
