Submitter | Handle | DEVINE_LAB | Submitter SNP ID | INDEL_GP35_WGS_197486 | RefSNP(rs#) | rs869091469 | Submitted Batch ID | EMORY_INDEL_GP35_WGS | Submitted Date | Jan 24, 2006 | Publication Cited | [1] An initial map of insertion and deletion (INDEL) variation in the human genome | First entry to dbSNP | Jan 24 2006 12:00:00:000AM |
| Resource Links | GenBank Accession | NT_016297
| 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 | METHOD_WGS | Ascertainment Samplesize | 2 | Population | N.D. |
| Allele | Observed Allele | -/CCA | Ancestral Allele | CCA | Allele Origin | N/A | SNP Class | DIV | CpG Code | N.D. |
| | Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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>gnl|dbSNP|ss50017587|allelePos=401|len=801|taxid=9606|alleles='-/CCA'|mol=Genomic CCAGTATTTT TTGATATTTT AGTAGCCCCA GTTCTATAAG TGTATTGTTA TTTTCAACTC
ATTGAAGACT TGTAGTATAG TCCATGTGTT TCCTTTTTAA GGGTGTAAAT ACAGTCTTTT
GAATGGCTGA TCAAATAAAT GTTTCATCAT GTCACTTTTT TGGTAAATCA GCACTTTACC
GAAGTTTATT TCATGTGTTT GTATGCTTGT GTTTACTAAG AACACTGGTT GATTTAAGGA
CTTTTTGGGG TGGCCTTATA AGAGCCTTTG TAAAGATAGC TGACGCTTAC TGGATTCTGG
TTATGAGAGA TTATAAGTGG CCGTTCTTAG AGTGTGTTAA AATACAGCCA ACAAGATAAA
TGTGAAAAAG CAAGGTGCAG AATAGTGTGG AAGAGGCCAT
N
TTGTGTCAAA AAGAAGGGCA TGTGTGTATT TGCCTGTATG GGTAAAAGGT TTCATGAGAA
ATTGGTAAAA TTGATTGCTT TCTGTGTAGA GAGTTGGGTG TCTGGGGTAT AGATATTTTT
TGAATTTTGT GTCATACAAA TGTGATTTAC TTAAAGGCAT CATTTGGCCT CTTTCCCTTA
AGACAGTGTT TGGAAATTTG TCAGATGTTT CTTTTTATTA ATTAATATTT ATTTTCTTTG
TTTTAGATGT TTGTTTTTAA ATATGAGTGT GAATTTTAAG TAGTTTTAAA TAATATTCCA
AAGTTGTTAG GCATGGAATA TTGATGTAAA GTACATTTTA TAATTAGTTA TTTTATGAGT
AGGATTACAT AAGTAAATTA TTAATTGTGA GGATATAAAC
There is no frequency submission for ss50017587.
No sufficient data to compute Hardy-weinberg probability for ss50017587.
There is no individual genotype data for ss50017587.
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