SNP Browser for Human [Homo spaiens] Genetic Disorders

  Home
  About us
  About Database
  SNPs ?
  Genetic Disorders ?
  Genetic Disorder List
  Genes List
  SNP Registry
  Acknowledgement
  References
  Our Team
  Contact us


ID 32
OMIM_ID 271150
Disease SPINAL MUSCULAR ATROPHY
Gene

SMN1

SNP_ID

rs2457869

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/G
Orientation fwd/B
Chr-Number 5
SNP type S
Length 401
5' Near Seq 30 bp cagtggtgcaatctcagctcactgcaacct
3' Near Seq 30 bp tgctatccgggttcaagcggttctcgtgcc
Fasta Sequence TTTGCATATT ATTTTGCCCT TTGGCCCATA TTTTGATATG GATGCCACCA TAGCATTTTG TGTATGTGCA TGTGTATTCC CACTTAATGT CACATTTTTC ATGTCTTTAC ATAttcttat ttttgtttgt ttttgagaca gagtctcgct ctgctgccca cgctggagtg cagtggtgca atctcagctc actgcaacct S tgctatccgg gttcaagcgg ttctcgtgcc tcagccacgt gagtagttgg gattacaggc atgtggcacc atgccccact aagttttgta tttttagtag agatggagtt tcaccatgtt ggccaggctg gtctcaaact cctgccctca agtgattcga ccaccctggc ctcccaaagt gctgggatta cagccgtgag
     

© 2008, IBI Biosolutions Pvt Ltd. INDIA