|
|
| ID |
70 |
| OMIM_ID |
143100
|
| Disease |
HUNTINGTON DISEASE |
| Gene |
HTT
|
| SNP_ID |
rs398982
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
fwd/T |
| Chr-Number |
4 |
| SNP
type |
R |
| Length |
1022 |
| 5'
Near Seq 30 bp |
tcccccgccgacgcctggagcggggcgaca |
| 3'
Near Seq 30 bp |
ccggccgtggactctgagccgaggtggcct |
| Fasta
Sequence |
ATGAATGGGG CTCTGGGCCG CAGGTAAAAG CAGAACCTGA GCGGCCGTCC ATCTTGGACC
CGTCCCGGCA GCCCCCACGG CGCCTTGCGT CCCAGACGCT gcgccggcgg aggcggggcc
gcgccggcgg aggcggggcc acgccggccA GCATGATTGA CAGCCCTAGC CTGCGGACTC
TGCCAATGGC TGGCCAGGGA ACCAGCCCGC CCCTGCCCCC GCAGGTTCTG CCTCACACAG
CAAGGCCGCT GACAGCGCAG CGCCCCACCC GGGCGAAGGC GCGGGGCTCA ACGGAGAGgg
gacggggcgt ggtgagactg taatggggtg aggcgaagct gtgtgtgaag tgtcgcggcg
aggcgggacg aggaagggac ggggcgggac tgcatggtaa gggaggcgtg gcgatgcggg
gggcgtggcg atgcgggggg cgtggtgagg taggggcgtg gcgaggccgg ggcggggcac
agcagggAGG CCGCCTGAgg ggcggggcga gacgggggcg gggcggggcg ATGCTGGGGA
CGGGGACATT AGGCAGGCCG GCTGAggggc ggggcggctg aggggcggac gggatagggg
aggggactgg ccggtgaggg ttggggaggc tgggggcggg gcaggaaggt gagaggtggg
gcgagggagg ggtggggcgc ggaggggcag ggccatggag gggctcgccc atgaaggacg
gggccatgga cggggcgggg cCGTGGAGGG GGCGCCGAGC GCGGGCGCAG GCCCATGCGG
AAAGGATCCC CCGCCGACGC CTGGAGCGGG GCGACA
R
CCGGCCGTGG ACTCTGAGCC GAGGTGGCCT TGGGGTTTGC CCTCCCGCCA CACTGGCCCG
TGGCCAGAGC CATACTCACC CGGACAGCCC TGCGGGGAGC CAGCTGCGGG GCTCTCTGCA
CGGGGAGAGG GTGGGCGAGC TCCTGCGCAG AGCGCAGAGA ATGCGCGTGG TCGGCACGAC
CTGAGGACCC CAAGTGTGAC CCCCA
|
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