SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 108
OMIM_ID 160900
Disease DYSTROPHIA MYOTONICA
Gene

DMPK

SNP_ID

rs12981796

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number 19
SNP type Y
Length 498
5' Near Seq 30 bp gaagcggctcaagcggccggcgtggcccgc
3' Near Seq 30 bp tggagcagcgcctcgcagacgcacgccacc
Fasta Sequence GCGCGCAGGT AGAGGTCCTG CAGGAAGGCG TGGTGGGCGG CGGGGAAGGG GCGGCTCTCG AGTAGCCGGT AGAGCTCGGC GTACTCGCCC CGCTGGAAGG CCACCAGGGC CCGCGCGCGC AACACCGGGT CGCTGCCACG TAGGCGCTCG GCCGGGGGCA GTGCGCCCAG GAAGCGGCTC AAGCGGCCGG CGTGGCCCGC Y TGGAGCAGCG CCTCGCAGAC GCACGCCACC TGCTCGGGCG AGAAGCGGAG GCCCGTGGGC GGTTCGGAAG CGGCCTCGGG GGGCGACCCG GGGACGCCCG GGGATCCCGG GCCCTCAGCT Cccgcagccg ctgcgcccgc cccggccccg gccgccgccg ccgcctcacc ctcggccgcc TGCAAAGTCT GCAAGAGCTG GCGCGCTTCC TCCTCCTCCT CTTCGGTcgc cgccgccgcc gccaccgcct cccccccagc cgccgGCCCC GCGCTCGGCT CCGCAGGCAA GGTAGCC
     

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