Submitter | Handle | DEVINE_LAB | Submitter SNP ID | INDEL_GP35_WGS_555775 | 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_026437
| 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 | AC/- | Ancestral Allele | AC | 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|ss50295054|allelePos=401|len=800|taxid=9606|alleles='AC/-'|mol=Genomic CATTGGTAAT TTTGTTAGAT ATAACCAAAT TGTTTTCTGT AATCTTACAC TAATTTACAT
TCTTCCCAGC AAGATATCAG CATGTGTCTT TCAGCACATC CTCACCAATA TTTTAATGTT
GCTAATCTGA TAGGTAAAAC ATGGTATTTC AGTGTGATTT AATTTTTAAT TCTGTTATTG
AAAGTGAGGT TGAAAATATT TTCATATATT TAAAAGGCAG TTGTATTCTC TTTTGTATAA
TCTTTATTAT AATACTTTTT CTTTATGAAG GTTTTGTGAA CTTTGTCCAG TCTTTTTGAT
TTGTAGAAAA TAGTGTGCAT ATTTGCAAAT ACTTTTCTTG GTTTGCTGTT TATCTTTTAA
CTTTGTTTAT AGCATTTTCT ATTTCAAGTA GGAATGTAAA
N
AGTTTTATAG TGAAGTTTGA TTTTTTTTCT CTTATAGGTT TTGTGTCTTT TTTAAAAAAA
TTATTTATTT ATTTTTTATG AGATGGAGTT TCGCTCTTTT TGCCCAGGCT GGAGCACAAT
GGCATGATCT CGGCTCACTG CAACCTCCGC CTCCCCGGTT CAAGCAATTC TCCTGCCTCA
GCCTCCTGAG TAGCTGGGAT TACAGGCATA TGCCACCACT CCCAGCTAAT TTTGTATTTT
TAGTGGAGAC GGGGTTTCTC CATGTTGGTC AGGCTGGTCT TGAACTCCCA ACCTCAGGTG
ATCTGCATGC CTCAGCCTCC CAAAGTTCTG GGATTACAGG TGTGAGCCAC TGTGCCCCCC
AGATTTATTT ATTGTACTTT AAGTTCTGGG ATACATATG
There is no frequency submission for ss50295054.
No sufficient data to compute Hardy-weinberg probability for ss50295054.
There is no individual genotype data for ss50295054.
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