NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Details: ss491283800           
Submitter
HandleEXOME_CHIP
Submitter SNP IDnonsyn_27_chr_1_874456
RefSNP(rs#)rs149677938
Submitted Batch IDproposed_content
Submitted DateMar 05, 2012
Publication CitedN.D.
First entry to dbSNPMar 5 2012 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodCOMMUNITY_COLLABORATION
Ascertainment SamplesizeN.D.
PopulationN.D.
Allele
Observed AlleleG/A
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss491283800|allelePos=201|len=401|taxid=9606|alleles='G/A'|mol=Genomic
 TCTGCGCTGA AGGCTGGGGC TGCCAGGGCT GGGCAAGGCC TGTACTCACC AGGACCAAGG
 GCCCCCTGAG AGATGGTGGG TGCGGTCCAG GCTGAGCTGG AGCAGGGGCT GGGTTCCCCT
 TCCATTCCTT GAGATGCAGG TGGGCACTCA CTACCCTCCC GCAGGTGACC TGTTGGGCAA
 GAGGCTGGGC CGCTCCCCCC
 R
 TATCAGCAGC GACTGCTTTT CAGAGAAGAG GGCACGAAGC GAATCGCCTC AAGGTAAGAG
 CGTGGCTGGG ACGAGAGACA GGTCACCAGG GGAGGGGGCA GTCCCTGAGG GTCCCCTGGA
 CCTCGAGCAG GCACTCTAGA GGGGCGTGGT CCTCGGCAGT GCCTGGAGAA ACCTCTCACC
 CCGGGTCCTC CCCAGCAGAG

  Submitted Frequency for ss491283800 back to top
There is no frequency submission for ss491283800.


  dbSNP summary of Genotypes for ss491283800 back to top
No sufficient data to compute Hardy-weinberg probability for ss491283800.


  Submitted individual genotype for ss491283800 back to top
There is no individual genotype data for ss491283800.