|
|
| ID |
SNP39.147 |
| OMIM_ID |
607014
|
| Disease |
Hurler Syndrome |
| Gene |
IDUA
|
| SNP_ID |
rs935966
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome 4 |
| SNP
type |
Y |
| Length |
768 |
| 5'
Near Seq 30 bp |
cagggtgggagctggaagactggctggggg |
| 3'
Near Seq 30 bp |
catgggggttgcccagagaggtatggtgcc |
| Fasta
Sequence |
>gnl|dbSNP|rs935966|allelePos=501|totalLen=768|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=129
GCAGCAGGGA GGCAGCTGGT GGGCCTGAGA CAGAATAAGG GTGGATATCA TGGGATATGA
GGCTCCATGG GGCTCTGGAA GTGACTGCTT TGAGGATGGG ACCCTGACCC AGAGCGAAAC
AAGGATCCCT TTCAAGGTTC TGAGCTGAGC AGTGCCAGGG CAtttttctt ttttcttttt
tttttttttg agacagagtc tcactctgtt gcccagcctg gggtgcagtg gcgcgatctc
ggctcactgc aagctccccc tcccgggttc acaccattct cctgcctcag cctcctgagt
agctgggact acaggcgccc gccaccacgc ccggctaatt tttttgtatt tttagtagag
acggagtttc accatgttag ccaggatggt ttccatttcc tgacctcgtg atccgcccac
cttggcttcc AGAGCATTTT TCAAGGATCC CTCTGGCAGC TCACTGGAGT CAGGGTGGGA
GCTGGAAGAC TGGCTGGGGG
Y
CATGGGGGTT GCCCAGAGAG GTATGGTGCC CAGACTGGGT GGTGGCTGTG CAGGCTGTGA
GCAGAGGGAC TGATGAGGTT TGAGGTGAGC TGGGGGGTGA GGTGGGGGGT CGGGGGGTCG
TACAGGGCAA CTGTGGATTT CAGCTTGGGC AGCTAGGCGG GTGGATGAGC TTGGAGTGAG
ACTGGTCTCG GTTTTGGCCA TGTGGAGTTG GACATCTGAG GGTGAACTGA GTGAGGAGAT
TGGTGTGCAA GGGTCTGGAG TTGTGAG
|
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