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 378
OMIM_ID 601859
Disease AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME
Gene

FAS

SNP_ID

rs7474952

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/G
Orientation fwd/T
Chr-Number 10
SNP type R
Length 401
5' Near Seq 30 bp gcaacgaaccctgactccttcctcaccctg
3' Near Seq 30 bp cttctccccctccctacccgcgcgcaggcc
Fasta Sequence CAGGACCTCT GCGCTCTGAG CTCCATTCTC CTTCAAGACC TCCCCAACTT CCCAGGTTGA ACTACAGCAG AAGCCTTTAG AAAGGGCAGG AGGCCGGCTC TCGAGGTCCT CACCTGAAGT GAGCATGCCA GCCACTGCAG GAACGCCCCG GGACAGGAAT GCCCATTTGT GCAACGAACC CTGACTCCTT CCTCACCCTG R CTTCTCCCCC TCCCTACCCG CGCGCAGGCC AAGTTGCTGA ATCAATGGAG CCCTCCCCAA CCCGGGCGTT CCCCAGCGAG GCTTCCTTCC CATCCTCCTG ACCACCGGGG CTTTTCGTGA GCTCGTCTCT GATCTCGCGC AAGAGTGACA CACAGGTGTT CAAAGACGCT TCTGGGGAGT GAGGGAAGCG GTTTACGAGT
     

© 2008, IBI Biosolutions Pvt Ltd. INDIA