|
|
| ID |
SNP39.106 |
| OMIM_ID |
607014
|
| Disease |
Hurler Syndrome |
| Gene |
IDUA
|
| SNP_ID |
rs5855690
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/G
|
| Orientation |
fwd/T |
| Chr-Number |
chromosome 4 |
| SNP
type |
N |
| Length |
401 |
| 5'
Near Seq 30 bp |
tgagccggggccgctggggtggccgccagg |
| 3'
Near Seq 30 bp |
ccctccaggctggggagcggctcctgcgaa |
| Fasta
Sequence |
>gnl|dbSNP|rs5855690|allelePos=401|totalLen=801|taxid=9606|snpclass=2|alleles='-/G'|mol=Genomic|build=114
CTGCCACAGC CGTGGAGGGC GGACGTGACC TACGCGGCCA TGGTGGTGAA GGTGGGCCGG
CCCAACGCCC TGCGCGCCCC CCGGCCACCT TCCTCCCGAG ACGGGACAGG CGAGCGGTGG
CCGCGCCACC CGGTCCCAGC TGCCCTGGAC ACCCGCAGGT CATCGCGCAG CATCAGAACC
TGCTACTGGC CAACACCACC TCCGCCTTCC CCTACGCGCT CCTGAGCAAC GACAATGCCT
TCCTGAGCTA CCAGCCCGCA CCCTCTTCGC GCANGGACTC ACGCGCGCTT CCAGGTCAAC
AACACCCGCC CGCGCACGTG CAGCTGTTGC GCAAGCCGGT GCTCACGGCC ATGGGGCTTG
GGCTGCTGGG TGAGCCGGGG CCGCTGGGGT GGCCGCCAGG
N
CCCTCCAGGC TGGGGAGCGG CTCCTGCGAA GGCCCCGCTG CGGGGAGCGC ACTTCCTCCA
GCCGCGCGCT TCCCGGGGTC GGCCTCCGCG TGGCGGGGCC TGGGGACTCC TTCACCAAGG
GGAGGGGGAG CGAGTGGTGG GAGGCCCGGC CCTGGGTCGG GGGGCGGCTG GGCAACGACC
CCACGCGGCG ACGGCCCCCC CCCGCCCCGC AGATGAGGAG CAGCTCTGGG CCGAAGTGTC
GCAGGCCGGG ACCGTCCTGG ACAGCAACCA CACGGTGGGC GTCCTGGCCA GCGCCCACCG
CCCCCAGGGC CCGGCCGACG CCTGGCGCGC CGCGGTGCTG ATCTACGCGA GCGACGACAC
CCGCGCCCAC CCCAACCGCA GCGTCGCGGT GACCCTGCGG
|
|
|
