Submitter Handle LUNTER Submitter SNP ID CEU_5_63847294-63847295 RefSNP(rs#) rs140297030 Submitted Batch ID indel_calls_from_1000_genomes_pilot_1_CEU Submitted Date Nov 21, 2012 Publication Cited [1] The Origin, evolution and functional impact of short insertion-deletion variants identified in 179 human genomes First entry to dbSNP Nov 21 2012 12:00:00:000AM Resource Links Submitted Gene Name N.D Submitted Gene ID N.D. Submitted SNP Synonyms N.D Submitted linkout N.D Assay Species Homo sapiens Molecular Type Genomic Method ILLUMINA_SHORT_SEQUENCE_DATA Ascertainment Samplesize 358 Population N.D. Allele Observed Allele -/ACACAC Ancestral Allele N.D. Allele Origin N/A SNP Class DIV CpG Code N.D. Validation Validation Status Not Validated HWE Goodness of Fit not applicable Variation Frequency Submission N.D. Genotype Summary N.D. Genotype Submission N.D. Haplotype N.D.   Fasta sequence   (Legend) >gnl|dbSNP|ss551503560|allelePos=26|len=51|taxid=9606|alleles='-/ACACAC'|mol=Genomic CATTTAATTA CTTGCCTATA TGCAT N ACACACACAC ACACACACAC ACATA   Submitted Frequency for ss551503560 There is no frequency submission for ss551503560.   dbSNP summary of Genotypes for ss551503560 No sufficient data to compute Hardy-weinberg probability for ss551503560.   Submitted individual genotype for ss551503560 There is no individual genotype data for ss551503560.

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