SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 112
OMIM_ID 160900
Disease DYSTROPHIA MYOTONICA
Gene

DMPK

SNP_ID

rs643226

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/T
Orientation fwd/B
Chr-Number 19
SNP type W
Length 601
5' Near Seq 30 bp aaaaaaaaaaaaaaaaaaaaaaaagctggt
3' Near Seq 30 bp taaagcagagagcctgagggctaaatttaa
Fasta Sequence GATTCCTCTT GGCTCTCGGA GCCGCAGGGA GTGTGTCTTC CCGCGCCACC CTCCACCCCC CGAAATGTTT CTGTTTCTAA TCCCAGCCTG GGCAGGAATG TGGCTCCCCG GCCAGGGGCC AAGGAGCTAT TTTGGGGTCT CGTTTGCCCA GGGAGGGCTT GGCTCCACCA CTTTCCTCCC CCAGCCTTTG GGCAGCAGGT CACCCCTGTT CAGGCTCTGA GGGTGCCCCC TCCTGGTCCT GTCCTCACCA CCCCTTCCCC ACCTCCTGGG AAAAAAAAAA AAAAAAAAAA AAAAGCTGGT W TAAAGCAGAG AGCCTGAGGG CTAAATTTAA CTGTCCGAGT CGGAATCCAT CTCTGAGTCA CCCAAGAAGC TGCCCTGGCC TCCCGTCCCC TTCCCAGGCC TCAACCCCTT TCTCCCACCC AGCCCCAACC CCCAGCCCTC ACCCCCTAGC CCCCAGTTCT GGAGCTTGTC GGGAGCAAGG GGGTGGTTGC TACTGGGTCA CTCAGCCTCA ATTGGCCCTG TTTCAGCAAT GGGCAGGTTC TTCTTGAAAT TCATCACACC TGTGGCTTCC TCTGTGCTCT ACCTTTTTAT TGGGGTGACA
     

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