|
|
| ID |
SNP39.011 |
| OMIM_ID |
607014
|
| Disease |
Hurler Syndrome |
| Gene |
IDUA
|
| SNP_ID |
rs60211784
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
chromosome 4 |
| SNP
type |
R |
| Length |
866 |
| 5'
Near Seq 30 bp |
ggcaccatacctctctgggcaacccccatg |
| 3'
Near Seq 30 bp |
cccccagccagtcttccagctcccaccctg |
| Fasta
Sequence |
>gnl|dbSNP|rs60211784|allelePos=366|totalLen=866|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=129
CAGACCCTGG CCAGCCTGGT CTCTGCTTCT CACTCCAGGC TCAAGGCTGG CTGCTATTCC
ATTCACCCCA TTCCCTTTCC CTCAGGCCAG AAGCATCACT CACAACTCCA GACCCTTGCA
CACCAATCTC CTCACTCAGT TCACCCTCAG ATGTCCAACT CCACATGGCC AAAACCGAGA
CCAGTCTCAC TCCAAGCTCA TCCACCCGCC TAGCTGCCCA AGCTGAAATC CACAGTTGCC
CTGTACGACC CCCCGACCCC CCACCTCACC CCCCAGCTCA CCTCAAACCT CATCAGTCCC
TCTGCTCACA GCCTGCACAG CCACCACCCA GTCTGGGCAC CATACCTCTC TGGGCAACCC
CCATG
R
CCCCCAGCCA GTCTTCCAGC TCCCACCCTG ACTCCAGTGA GCTGCCAGAG GGATCCTTGA
AAAATGCTCT GGAAGCCAAG GTGGGCGGAT CACGAGGTCA GGAAATGGAA ACCATCCTGG
CTAACATGGT GAAACTCCGT CTCTACTAAA AATACAAAAA AATTAGCCGG GCGTGGTGGC
GGGCGCCTGT AGTCCCAGCT ACTCAGGAGG CTGAGGCAGG AGAATGGTGT GAACCCGGGA
GGGGGAGCTT GCAGTGAGCC GAGATCGCGC CACTGCACCC CAGGCTGGGC AACAGAGTGA
GACTCTGTCT CAAAAAAAAA AAAAAGAAAA AAGAAAAATG CCCTGGCACT GCTCAGCTCA
GAACCTTGAA AGGGATCCTT GTTTCGCTCT GGGTCAGGGT CCCATCCTCA AAGCAGTCAC
TTCCAGAGCC CCATGGAGCC TCATATCCCA TGATATCCAC CCTTATTCTG TCTCAGGCCC
ACCAGCTGCC TCCCTGCTGC
|
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