|
|
| ID |
SNP39.031 |
| OMIM_ID |
607014
|
| Disease |
Hurler Syndrome |
| Gene |
IDUA
|
| SNP_ID |
rs57431667
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
C/T
|
| Orientation |
fwd/B |
| Chr-Number |
chromosome 4 |
| SNP
type |
Y |
| Length |
401 |
| 5'
Near Seq 30 bp |
aaccctgagcgtcaggtcaggcccatccct |
| 3'
Near Seq 30 bp |
ctgagctgagggacggtgcattggggccca |
| Fasta
Sequence |
>gnl|dbSNP|rs57431667|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=129
GGCACTTGGG TGTGTGGGGC CTTCTGGAAA CACAGAGACC CTCGTGCACT TGGCCAGAGC
CGCTGGCTCC TACCAGCAGG GTGGGCACCG GGCAGGCCTG GGCATAGGGA GTCCTCTTGG
CACCTTGGAG GCTGCATGAT GGCGGGGGAC CCTTGTTCAA ATAAGATGTC AACCCTGAGC
GTCAGGTCAG GCCCATCCCT
Y
CTGAGCTGAG GGACGGTGCA TTGGGGCCCA GCCAGCACTG TGGGCCAGCC TGTCTCGGAG
GCAGAGGTTC TTGATTTCTG AGTGTTTGGG TCCTGCGTGT GATCAGAGGG CCTCCTTTCC
CAGTTGGGGT TCCCCGGTTT CCCCAGGGCA GCTGTGGCAC AAGAGTGCAG CTCTTGGGTG
GCTCCTCCCT GGGAAGGGTC
|
|
|
