Submitter | Handle | SI_MHC_SNP | Submitter SNP ID | AL662890.3_17369_i2TA | RefSNP(rs#) | rs376138106 | Submitted Batch ID | 2003_09_18 | Submitted Date | Sep 22, 2003 | Publication Cited | [1] Complete MHC Haplotype Sequencing for Common Disease Gene Mapping | First entry to dbSNP | Sep 22 2003 12:00:00:000AM |
| Resource Links | GenBank Accession | AL662890.3
| 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 | MHC_XM20030904 | Ascertainment Samplesize | 2 | Population | N.D. |
| Allele | Observed Allele | TA/- | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | DIV | CpG Code | Unknown |
| | Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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Comment | sequence: AL671879.2position: 173474quality: [40] |
>gnl|dbSNP|ss12704313|allelePos=401|len=801|taxid=9606|alleles='TA/-'|mol=Genomic aaattagtat atcgaaaaga tatctacact gtcatcttta ttgcagcact attcacaata
gccaagattg ggaagcatcc taagtaccca tcaacagata aatgaataaa gtaaatgtgg
tacgtataca caacggggta ctattcggcc atgaaaagaa tgaggtcttg tcatttgcaa
agcggatgga actatgttct gtgcgggaaa tgcgagaggg gagaagaaaa gacacacaca
caataccttt aagggtaaat aacctttatc ccacgtaaac ggcaatgcag atataataaa
caaatgatac aataagcaaa ttgcaatggg aaggggagaa gggaaaagat atatatatat
atatatatac acacactcac caaatatata tatatatata
N
aatatatata tttatatata tgtacactca caagactatg aaggattcat caccacaccg
ggaagcaaca gccccggctc cagagtcggc cactcgtcca tgcacagaga aggagaggtc
tcatgaagct cacgagagcc cttcgcgact gagctcaagg aacaagaaaa ggtcaacttg
tttttgcgat tgtctgttgt ttttcaataa ctaacgtata ggaatagatt gaaatagaga
tttctccaaa acagcactgg atgaacacct caaggggttc atacaacctg ttcaggattt
ggtgaccatt gtttgtgtcc acgttcaatt gagttcaaat ttaatacgta acttttcctc
cacaaactag aggacattaa gttaagctat acacagaaaA
There is no frequency submission for ss12704313.
No sufficient data to compute Hardy-weinberg probability for ss12704313.
There is no individual genotype data for ss12704313.
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