|
|
| ID |
SNP39.146 |
| OMIM_ID |
607014
|
| Disease |
Hurler Syndrome |
| Gene |
IDUA
|
| SNP_ID |
rs1131853
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
chromosome 4 |
| SNP
type |
R |
| Length |
401 |
| 5'
Near Seq 30 bp |
cagtggccggtcctcagggttctccagggg |
| 3'
Near Seq 30 bp |
gctggggacgctcggcccgacctcagggcg |
| Fasta
Sequence |
>gnl|dbSNP|rs1131853|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=111
TCCGGGCCGC GGCGCGGGTT AGGGGACTGC CACTTGCCTG CCCGGGCGGC TTCTCGGGGC
GCGCACACAC GTGCACCAGC AAAAGCGACG GCAGCCGCAG CGCGGGGCGC AGGGTCAGGC
GGCCGCCGGC GGGTAAGGGG CGGGGCGCCG CGGCCACCGG GTCCTGGGCG CAGTGGCCGG
TCCTCAGGGT TCTCCAGGGG
R
GCTGGGGACG CTCGGCCCGA CCTCAGGGCG AACGCccccg gcccaccgct ccacctccca
cccacaccgc ctcggagccc ccgccccgga ccccaccccc ccgggacccc ggcccggccc
ggcccctcgc ccctccgcgg cccaccTACC TCAGCCGCGC GCATGCGCCG GAACTGCTCT
GCCGTGGGGA AGACGGGCCG
|
|
|
