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: ss157711265           
Submitter
HandleGMI
Submitter SNP IDGMI_SNP_38991992
RefSNP(rs#)rs55694638
Submitted Batch IDGMI24june2009snp_6
Submitted DateJun 24, 2009
Publication Cited[1] A highly annotated whole genome sequence of a Korean Individual
First entry to dbSNPJun 24 2009 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodAK1
Ascertainment Samplesize2
PopulationAK1
Allele
Observed AlleleC/T
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.
Comment
Chromosome-16

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss157711265|allelePos=101|len=201|taxid=9606|alleles='C/T'|mol=Genomic
 AACAAAGTGC GCACTTCAAA GGTGGCACCA GATTTCCTAC GGCAGAGCCC ACGGTGGGGT
 CCCTTCCTGA TGGGTGGACC CAGTTCCTGT TTTGCACCTG
 Y
 TTCCCCGTGG CGTGCTGGAT GCCTGCGGCT CTGCCTCCAG CTCTGTCTGT CCCAGATGCC
 AGGTGTGCTG GGGCCTTTGA TCTTCAGCCT ACACTGGGGG

  Submitted Frequency for ss157711265 back to top
There is no frequency submission for ss157711265.


  dbSNP summary of Genotypes for ss157711265 back to top
No sufficient data to compute Hardy-weinberg probability for ss157711265.


  Submitted individual genotype for ss157711265 back to top
There is no individual genotype data for ss157711265.