|
|
| ID |
31 |
| OMIM_ID |
271150
|
| Disease |
SPINAL MUSCULAR ATROPHY |
| Gene |
SMN1
|
| SNP_ID |
rs150410
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/C
|
| Orientation |
fwd/T |
| Chr-Number |
5 |
| SNP
type |
M |
| Length |
1337 |
| 5'
Near Seq 30 bp |
agtagctaggactataggcgtgcgccacca |
| 3'
Near Seq 30 bp |
gctcagctattttttgtatttagtagagac |
| Fasta
Sequence |
CGCAGCGTGG GGCCCCGTCC CTTCTTAAGA GTGACGACTT CCGCCGCCCG GGGCTTCTGG
GAGCGGAACA GTACGGTGGC CGGGAGGACC GCTTGTAGTA ACTTCTCACG CTTTCTACGA
GTGGTTATCG CCCTCCCACA TTTGTGGCGT GTATATTTTT CATTTCTCTC AATCCTTTCA
TTTCACTGTG TTATATTTCC tttccttttt tttttgtttg tttgttttga gacagagcct
cgccctgtcg ctcaggctgg agtgcagcgg cgcgatctcg gctcactgca gcctcgactt
cttgggctca agcgatcctc ccacctcagc ctccccagta gctaggacta taggcgtgcg
ccacca
M
gctcagctat tttttgtatt tagtagagac ggggtttcgg catgttgctt aggcctcgtc
tcgaactccA gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt AGATATTTAT
TCCCCCTCCC CCTTGGAAAA GTAAATGTAA GCTCCTACTA GGAATTTAAA ACCTGCTTGA
TCTATATAAA GACAAACAAG GAAAGACAAA CATGGGGGCA GGAAGGAAGG CGGCAGATCC
TTAAACACTA GAAGATATTT GATCCCCCAA CCTTAtttgt tgtttgtttt gagacggagt
ctcgctctgt cgtcagagtg cagtggcacc atctcggctc attgcagcct cgacctcccg
agctcaagcg atcctcccgc ctcaacctcc caagtagcta ggaccacagg ggcacgccac
cacacccggc tagtttctgt atgttttgta gaggcggcgt ttggagcata ttgtgtaggc
tggtctcgaa ctcctgagct caagatattc cgcccgcctc tggcatccca aaatgctggg
attacaggtg tgagccacct cgcccagccT CCAGTAttct tttttttttt tgcgacagag
tattgctctg tcacccaggc tggaatgcag tggcgtgatc tcagctcact gcaacctctg
cctcccaggt tcaagcaatt ctcctgcctc agccccccga gtagctggga ttacaggcgc
ccaccaccac acccggctaa tttttgtatt tttagtaaag atggggtttc accatgttgg
ccaggctggt cttgaactcc tgaccttgta atccgaccgc ctcggcctcc caaagtgctg
ggattacagg tgtgagccac cacaccgggc cTCCAGTATT CTTTATTAAG CATCTAGGGT
TGCTAAATGG CTTATATGTA CATAGTATAT ATATATTTTT AACTCCACGA AAGGAACTTT
GAGCTCTTCC
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