Submitter | Handle | DEVINE_LAB | Submitter SNP ID | INDEL_GP35_WGS_197477 | 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_022171
| 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 | T/- | 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. |
|
>gnl|dbSNP|ss50017579|allelePos=401|len=800|taxid=9606|alleles='T/-'|mol=Genomic TGGTTTCTTG GTAAAACTCA CACAAAACAG ATGGAGAAGA GTTTTTGTAT ATCAACATGA
ATGTTAATGT GATTTTTTTA AAGCCAACGA ACACATTTGT GTTCCTTGTG AGATCCTGTG
CATGAATTTG TCAGGTAATT TTTTTGACCT GAACATTCTC ATAATAGCTT CAATTTGCAC
AATGCAACCT CGTCATTTTG CAGATTTTCA AGGCTCACTT CAAAAACATG TTCCTTGAGG
CCTATTAACA TTTCTTTCCT AAATTGTCTA TTCATATGGT GCTTTTAAAA GTTAGATTAC
TTTTAGTAGA TTTATTAGAG CCGCACAGTT TAGAGTCAGT AGTCAATTAA AGTCCCTACT
TAAACTTCAG ACTAAGATTT TTTTTTTATT TAATATTTTA
N
TTTTTTCTTT TTGCTTTCAT GCAGACAGAC ATCTTGCAAG ACTTTAAGAT TCTTGGGCCA
TTTCTGTCAG GTTGTTCTGT GTTCTGTGCC TGCTTCCTCC CCATAGTAAT TTCAAAATAG
CTATCCTCAC CTCTGTAAGG TTTCCAAAAT CAAACTTGGG CTTCTGGCTA GCCTTTTCTG
GGTCTTGATT TTTCAGTGCT TTCCAGAGGC AATTGTTTGG AACCTCTTGG CACAGTTTCT
GTTTCTTCTT CCATGTACAG GCATGAAAGA TCTTTTGGTT GTTTTCTGGT AAAACTATCA
TAAAACAGTT GAAGCAAATG ACTATTGGTA GTTTTGTCAT TAACAGGGGT GCCTTCTAGT
TGTTTTGTTT CCTGGTAAAA CAGACCAAAC AGAGGGAGC
There is no frequency submission for ss50017579.
No sufficient data to compute Hardy-weinberg probability for ss50017579.
There is no individual genotype data for ss50017579.
|