Submitter | Handle | DEVINE_LAB | Submitter SNP ID | INDEL_GP35_WGS_197492 | RefSNP(rs#) | rs34302627 | 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_019273
| 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 | -/TGT | Ancestral Allele | N.D. | 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|ss50017592|allelePos=401|len=801|taxid=9606|alleles='-/TGT'|mol=Genomic ATGGGCCAAG GAGGACAGGA AAGCTCTCTG ACCCACAGGT ATCTGTGTTT AATATTCCAT
CCTAGTTTCT CTTTCTCTCT CTCCTCTTTC ACTTCTCTCT CTCTGTCTCT CTTTCTCTCT
CTCTCTCTCT TTCTTTTTGA CACAGGGTCT TGCTCTGTCG CCTAGGCTAG AGTATAGCAG
TGCAATCATG GCTCACTGCA GCCTCTACCT CCTGGGCTCA GACGATTCTT CCACCTAAGC
CTCTTGAATA GTTGGGACTA TAGGCATGCA GCACCACAGC TGGCTAATTT TTTGTATTTA
TTGTAAAGAT GGGATTCACC ATATTGTCCA GACTGGTCTT GAACACCTGA TCTCAAGTGA
TCCACCCACC TGGGCCTCCC AAAGTGCTGT GATTATATGG
N
AGCACCTAGC TCCATCCTAG TTTCTGACTC AAACCAATAT TTGTGTATAC AGCTCATCCT
CAGAATTGAT CTTCCATAGC CTAAACAGAG GTATGAGACA CAAGGAAAAT AGAGGTTACC
CAGAAGAATG TTTAGAGCAT CCTGCCATTC ATCTTGAGAA GATTCACTGT CTACAACCAG
AATTGAGTTG ACTTTGTCTT CCTCAGATGT GATTTTGATG TTCTTGTGAG GCGGGTTGGA
GTCAGAAGGG CCATGGCTAT TTGAATAAGT GATGGCACAT TCCTCCAGTG AGTCCTCAGG
GACTTCCTTT TCTTCAGCCT TCTGCTCCTC CCTGATGAGC CAGGTGGGAT AGAAATGACA
GAAGATTAAA CAGAGAGGGA TTGGATCCCA GGGAGACCTA
There is no frequency submission for ss50017592.
No sufficient data to compute Hardy-weinberg probability for ss50017592.
There is no individual genotype data for ss50017592.
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