Submitter | Handle | DEVINE_LAB | Submitter SNP ID | INDEL_GP35_WGS_197490 | RefSNP(rs#) | rs869065109 | 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_004487
| 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 | CTTTTT/- | Ancestral Allele | CTTTTT | 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|ss50017590|allelePos=401|len=800|taxid=9606|alleles='CTTTTT/-'|mol=Genomic CCTCACTTGT CTCATCTGTC AGACAGGGAT GGTGGTACCA AAAAAAGCCA ATGTGAAGGC
ACAAAGCCGC AGGAGGGTAA AATAACCATG ATGATGGGAT GGGACCTCAC TTAAACATTG
TGGTCACTTC ACTAAATGCT TTATGTGCAT CATTTAATCC TTGAAACAGC CCTAAAACAT
AGGGAAACTG AGGCACGGAG AGGTTCTATA GCCCACCTGA GGCCTCACAG GCAGTAAGTG
GCAGGGGTGG GACTATGGGA TTCGAGCCAG TTCTAGAGCC TCTCTGTTCT CCAGGGAGGC
AGCACAGCCA TCCCGGGAGA GGAGAGGCAC AGGGACACGT GGGAAACAGC AGGCCTCCTT
GGGGTTTCCT GCTGTCCTCC TGCTCATCCT CTTTCTTTTT
N
TTTGAGGGTG GGAACAAGAG GTGGGTGAGT GAAGTTGGAA TTAATGAGTC TGCCTGAATC
CTAGGGAGGG GGCAGGAAGG GAAAGCCCAG GTGGGGCTCT TCAGGATTAT AGGTGTCTTG
GAAACTGGGA GGCCAGGGGA GCACCCTTAG TGGAGGGTTC CCTATAATTT CAGTTCATTT
TTCTCTTGCA CATTCTGCTT GAGTAGATCA ATACCCCACA AATATATCCT GTGTGTATCC
TGAGGGGAGG CAGGGTTGAA GGAAGGTGGG AGGGAGTACA GTTGCAGATA GACGGGAGGA
GAGAGACTGA AGATAGAGGA GAGGCGGGGA GCCATGGTAG ACCCAGGGGC CAGGAGGGTG
GAAGAAGGCT GTGATCGAAC AGGGGCCTCA AGGCACAGC
There is no frequency submission for ss50017590.
No sufficient data to compute Hardy-weinberg probability for ss50017590.
There is no individual genotype data for ss50017590.
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