Submitter | Handle | DEVINE_LAB | Submitter SNP ID | INDEL_GP35_WGS_197476 | RefSNP(rs#) | clustering in process | 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_011651
| 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 | -/AG | Ancestral Allele | - | 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|ss50017578|allelePos=401|len=801|taxid=9606|alleles='-/AG'|mol=Genomic GAGGGAAATA CACACATATT CATACATATG TCCAAGTTTG ATGGGACAGA GACCATGCAC
CTGTAGTCCA TTTTTTTAAA AACTGAAAGT AGATGTATAA CTTTGGTAGA GAGGAGTTTC
AGTGAGGTAC ACACACACAC ACACACACAC ACACACACTT CAAGAATTTA GAAATATGAT
TTTCCTCTAA AAGCTAAACC AGTAAAAGCC AGCCACAATG GATGTGATGA TTGGATTGGA
GGACACAATC AAAAGACTGC CTGTCCAGGT ATGACAACAA AATATGCACA CACCCAACAC
ACCAGTCAAG GTTGAGTTGG GACCAGTCCA ATGAAAGGGA AGACAGGTCA TGTCCAGGCA
GAAGTATGGC ATGTGCAAAA ACTAGGAGGT GAGAGAGAGA
N
GAGCAATATG TATTCAGAGA TCTTAGAAAA GTTCAGTATG GCCAAAGCAT TGAAGATAGA
GTAGTAGCCA GGGGCGGGGC CCTGAAAGGT CTTGTCTGCC ACATCAAGGT TGATTGGACC
TTGTCTCCAG TACAGTGGGA AGCCAGACAT TGAGATGTTC TCATTCAGAC ATGGAAGCAT
TCAGATTTTA GGAAGGTGTC TTTGACTGCA GTGTATTGGA GTTGTCCCCA CACCCACTCC
ACAGCAGAGG AGGCTGCTGC AGATAACCAG AAGGGAGATG GCCTGGGCAA GGTAGGCAGG
AGTGGCATCT GGTAGGAGTG GACTGATGAG AGACATCTCA GAGGTACATG GATGGTGTCT
TAGTCCACTG GGGCTGCTAT AACAAAATAC CTTACACTGG
There is no frequency submission for ss50017578.
No sufficient data to compute Hardy-weinberg probability for ss50017578.
There is no individual genotype data for ss50017578.
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