|
|
| ID |
SNP39.092 |
| OMIM_ID |
607014
|
| Disease |
Hurler Syndrome |
| Gene |
IDUA
|
| SNP_ID |
rs10471250
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome 4 |
| SNP
type |
Y |
| Length |
601 |
| 5'
Near Seq 30 bp |
tcctaagtgtgagatgtggacagggctgaa |
| 3'
Near Seq 30 bp |
gctccagggtctcgtaccccagagtgtgag |
| Fasta
Sequence |
>gnl|dbSNP|rs10471250|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=129
ATTGAAGCCG AGGGTCTCGC AGAACCAGCT GATGTGCCGG GGCTCCATTT CCCCAAGACG
AGGACACTGA CATTGATGGG GCACAGCCCC GGAGGGAGGA GACCCTGGAC ACTCACCCCA
CCAAAGGTAC CTCCTTGTGG AAGCCGTCTG CCAAGCGCTG CTAGTTCCCC ACAGCCCTGG
GTGAGCCCAG GGAAGACTGG GCTGCAGTGC CCCCATTTGG AGGTGAAATG GGAGTGGAAT
GTAGTTGGGA TGGCCAGAGA GTAGGAGACA TCCTAAGTGT GAGATGTGGA CAGGGCTGAA
Y
GCTCCAGGGT CTCGTACCCC AGAGTGTGAG ATGCGGGCAG GGCTGAACGC TCTGGGGTCT
CGTACCCCTG AGTGTGAGAT TCGGGCAGAG CTGAACAGGC TCCAGGGTCT CATACCCCCA
TAGCCTCCAC CTGGGATGCC CTCTCCAAGT CTGATTTCTC CTCGAAGCCC CTGCCCTGTC
CTCCAGAGTC TGAGCCCTTG CTTCCACCCC AGCCCAACCT GGGCCCCAGT GGTCCCTGGG
AAGCAGCTGT TTGCTCAGCA GTTGGGAGCT GTGCTGTAAG AAGCGGTTGG CCAGTGGGTG
|
|
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