SNP Browser for Human [Homo spaiens] Genetic Disorders

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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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