|
|
| ID |
SNP39.012 |
| OMIM_ID |
607014
|
| Disease |
Hurler Syndrome |
| Gene |
IDUA
|
| SNP_ID |
rs60132156
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
G/T
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome 4 |
| SNP
type |
K |
| Length |
401 |
| 5'
Near Seq 30 bp |
ccttctcccttgaggacgcctgtcccctcg |
| 3'
Near Seq 30 bp |
aatgcaggcctcgtgggaattcagccccat |
| Fasta
Sequence |
>gnl|dbSNP|rs60132156|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='G/T'|mol=Genomic|build=129
TTCTCCCTTG AGGACGCCTG TCCCCTCGTA ATGCAGGCCT CGTGGGAATT CAGCCCATCT
GCAAGTGCAG TGGCAGGGCG GCCCCCTTCT CCCTTGAGGA CGCCTGTCCC CTCGTAATGC
AGGCCTCGTG GGAATTCAGC CCATCTGCAA GTGCAGTGGC AGGGCGGCCC CCTTCTCCCT
TGAGGACGCC TGTCCCCTCG
K
AATGCAGGCC TCGTGGGAAT TCAGCCCCAT CTGCAAGTGC AGTGGCAGGG CGGCCCCCTT
CTCCCTTGAC GACGCCTGTC CCCTCGGAAT GCAGGCCTCG TGGGAATTCA GCCCCATCGG
CAAGTGCAGT GGCAGGGCGG CCCCCTTCAC CCTTGACGAC GCCTGTCCCC TCGGAATGCA
GGCCTCATGG GAATTCAGCC
|
|
|
