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 SNP6.026
OMIM_ID 203450
Disease Alexander disease
Gene

GFAP

SNP_ID

rs60343255

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number chromosome 17
SNP type Y
Length 201
5' Near Seq 30 bp gctggcttcaaggagacccgggccagtgag
3' Near Seq 30 bp gggcagagatgatggagctcaatgaccgct
Fasta Sequence >gnl|dbSNP|rs60343255|allelePos=101|totalLen=201|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=129 CCTCTCCCTG GCTCGAATGC CCCCTCCACT CCCGACCCGG GTGGATTTCT CCCTGGCTGG GGCACTCAAT GCTGGCTTCA AGGAGACCCG GGCCAGTGAG Y GGGCAGAGAT GATGGAGCTC AATGACCGCT TTGCCAGCTA CATCGAGAAG GTTCGCTTCC TGGAACAGCA AAACAAGGCG CTGGCTGCTG AGCTGAACCA
     

© 2008, IBI Biosolutions Pvt Ltd. INDIA