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: ss488651931           
Submitter
Handle1000GENOMES
Submitter SNP ID20110521_exome_2788_chr1_11709892
RefSNP(rs#)rs114834790
Submitted Batch IDphase_1_exome_sites_20110521
Submitted DateFeb 10, 2012
Publication CitedN.D.
First entry to dbSNPFeb 10 2012 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodEXOME_CAPTURE
Ascertainment Samplesize2256
PopulationN.D.
Allele
Observed AlleleC/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|ss488651931|allelePos=201|len=401|taxid=9606|alleles='C/A'|mol=Genomic
 TCAACCTTTG CAGACCCGTG GCCCACGTGG CCTCAACCCC TGCAGTGGGG AGGCAGCACC
 CCCAGGCGGG GGGTTCCCCA GCTGGCTCTC CCCTCTGCCT TACCCCGCTC CTCCCAGCCC
 CATGCCACCC CAGGACCCTC TCACCAGTCC TTCACCACGA TGGCCGGCTG AGTCGTGTCC
 AGCAGCTCCT CCCAGTAGCC
 M
 TCAGCCTGCA GGTCAATGAC CTGTGCTTTG CGACACCACC TGGGAGAACT GGAGTTAGGA
 CAGAGCGAAC GCTCCCCCCT TCCCACCTCC TCCACCCCCT TCTCCTTACT CAAAGGAGGA
 GGCGAAGTAC TTCTTGACGC TCTCATCGTG GGTGAACTCC ACCCCACTGT CTCCAGGCAG
 CTCCTCCACC CTCCAGCCGT

  Submitted Frequency for ss488651931 back to top
There is no frequency submission for ss488651931.


  dbSNP summary of Genotypes for ss488651931 back to top
No sufficient data to compute Hardy-weinberg probability for ss488651931.


  Submitted individual genotype for ss488651931 back to top
There is no individual genotype data for ss488651931.