|
|
| ID |
SNP6.130 |
| OMIM_ID |
203450
|
| Disease |
Alexander disease |
| Gene |
GFAP
|
| SNP_ID |
rs1042465
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
chromosome 17 |
| SNP
type |
R |
| Length |
101 |
| 5'
Near Seq 30 bp |
acgacagaagggtccttccctctccccaag |
| 3'
Near Seq 30 bp |
cttggtgtcctttccctccactccttcctg |
| Fasta
Sequence |
>gnl|dbSNP|rs1042465|allelePos=51|totalLen=101|taxid=9606|snpclass=1|alleles='A/G'|mol=cDNA|build=86
GTTCTCCTCT CCCCTCTAAG ACGACAGAAG GGTCCTTCCC TCTCCCCAAG
R
CTTGGTGTCC TTTCCCTCCA CTCCTTCCTG CCACCTGCTG CTGCTGCTGC
|
|
|
