|
|
| ID |
SNP39.027 |
| OMIM_ID |
607014
|
| Disease |
Hurler Syndrome |
| Gene |
IDUA
|
| SNP_ID |
rs58132109
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/A
|
| Orientation |
fwd/ |
| Chr-Number |
chromosome 4 |
| SNP
type |
N |
| Length |
1001 |
| 5'
Near Seq 30 bp |
gagtgagactctgtctcaaaaaaaaaaaaa |
| 3'
Near Seq 30 bp |
gaaaaaagaaaaatgccctggcactgctca |
| Fasta
Sequence |
>gnl|dbSNP|rs58132109|allelePos=501|totalLen=1001|taxid=9606|snpclass=2|alleles='-/A'|mol=Genomic|build=129
TCCAAGCTCA TCCACCCGCC TAGCTGCCCA AGCTGAAATC CACAGTTGCC CTGTACGACC
CCCCGACCCC CCACCTCACC CCCCAGCTCA CCTCAAACCT CATCAGTCCC TCTGCTCACA
GCCTGCACAG CCACCACCCA GTCTGGGCAC CATACCTCTC TGGGCAACCC CCATGGCCCC
CAGCCAGTCT TCCAGCTCCC ACCCTGACTC CAGTGAGCTG CCAGAGGGAT CCTTGAAAAA
TGCTCTGGAA GCCAAGGTGG GCGGATCACG AGGTCAGGAA ATGGAAACCA TCCTGGCTAA
CATGGTGAAA CTCCGTCTCT ACTAAAAATA CAAAAAAATT AGCCGGGCGT GGTGGCGGGC
GCCTGTAGTC CCAGCTACTC AGGAGGCTGA GGCAGGAGAA TGGTGTGAAC CCGGGAGGGG
GAGCTTGCAG TGAGCCGAGA TCGCGCCACT GCACCCCAGG CTGGGCAACA GAGTGAGACT
CTGTCTCAAA AAAAAAAAAA
N
GAAAAAAGAA AAATGCCCTG GCACTGCTCA GCTCAGAACC TTGAAAGGGA TCCTTGTTTC
GCTCTGGGTC AGGGTCCCAT CCTCAAAGCA GTCACTTCCA GAGCCCCATG GAGCCTCATA
TCCCATGATA TCCACCCTTA TTCTGTCTCA GGCCCACCAG CTGCCTCCCT GCTGCCTGAT
TGTCATGTGT GCATTCCTGT TCCAGAGCCT TTGCACTGGC GATGCCATCT GCTGCCTGGA
TGTCTTCCTG CTGGCTGGTC CCGTTGCATG GTAGCCTTAG GTGTCTCCTC AGAGAGGTCC
CTCGCTGACC ATCAGGCTCC TCACTCCCTG TCGTATCCCC TTCACCAAAG ATTCCCATTC
CCTGACGACG CCTGTCCCCT CGGAATGCAG GCCTCGTGGG AATTCAGCCC ATCCGCAAGT
GCAGTGGCAG GGCGGCCCCC TTCCCCCTTG ACGACGCCTG TCCCCTTGGA ATGCAGGCCT
CGTGGGAATT CAGCCCATCT
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