Submitter | Handle | DEVINE_LAB | Submitter SNP ID | INDEL_GP35_WGS_197494 | 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_007592
| 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 | GT/- | 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|ss50017594|allelePos=401|len=800|taxid=9606|alleles='GT/-'|mol=Genomic TAGCTTCTAA TTCAGTAATT CTTTCTTCAG CTATGTTTCA TATACTTTTA AACCTATCCA
TTGAATCCTT AGTCTTGGGT ATTATAATTT TCAGTTCTAG AATTTTAATT TTTTTAACAA
AGTTTCAATT CCCTGCCAAA ATTCTCAAAC CATGTCTATT TCCATCATGT ATTTTTATCT
CTTTGAACAT AATAAGCATT GCTGTTTTTT TAATTATAAA ATCTGCATCT GATAATTCCA
ACATCTAGAA CCCCTGCTGT ATATGCTTTT ATGTTTGTTC ATGTTGTCCA GTCTCATGTG
TTTGGTTTTT GGTGTTGGTT TTGGTTTGTT GTGTGTATGT GTGTGTTTTA TTTGTTTTTT
TGTGAGTTGT TTTTGTTTGT GTGTGTGTGT GTGTGTGTGT
N
GTGTGTGTGT TCTGGACATT GCAGGTGCAA AGTTGTTTGT AGAAATTATC TGACACCAGG
ATGACATCTT CTTCCAGAGA GGATTTGCAA GACCCTGAGG GCACTAGCAA CATTGGATCG
CCTTAATCCA ATTTCAGGAA TTGAGATGAG TCTAAGCAGA GCGGCAGTCA CTGTAAGAAC
CTGTCTACTT CCAGTTTATC CTTAGTCCTC AGGCACAGCC CTTTGGGGTC TCAATCCAAA
GCAAGGAGGT TTACCAAATA CTCCTCTTGG TAGGCTTTGT CTCATATCCC CAGATCCTCA
AAAGCGCTGA TTAACCTTTC AACCTCTCAG TCACTCACTC CCTCCATTCC CAGAGGAAAA
GCATTTAAAA GCCAAGCTCA GCCAGGTGCA GTGACTTAA
There is no frequency submission for ss50017594.
No sufficient data to compute Hardy-weinberg probability for ss50017594.
There is no individual genotype data for ss50017594.
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