NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
View SNP Submission Batch
Submitter Handle:KWOK
Submitter Batch ID:8.4.98(4)
Submitter Method ID:3
Citation:SNPs from Human Chromosome 7p21-22 Overlapping Regions
Comment:SNPs from the overlapping genomic sequence between clones DJ1168D11 (accession no. AC004614) and DJ1110H13 (accession no. AC004141) on chromosome 7p21-22. These SNPs represent DNA sequence variations between the two donor chromosomes but the allele frequencies in the general population are not known. Furthermore, these SNPs are located within regions containing repetitive elements and are most likely not good candidates for genetic marker development.
Batch Total SubSNP(ss) Count:8


SubSNP(ss) Submitter
SNP_ID
SNP
Allele
Samplesize RefSNP(rs) ss2rs
Orien
Chr ChrPos Contig
Accession
Contig
Pos
ss44 700060 G/T 2 rs45 0 7 11546515 NT_007819.18 11536515
ss43 700059 G/T 2 rs44 0 7 11546563 NT_007819.18 11536563
ss42 700058 C/G 2 rs43 0 7 11546640 NT_007819.18 11536640
ss41 700056 A/T 2 rs42 0 7 11546724 NT_007819.18 11536724
ss40 700055 C/T 2 rs41 0 7 11547118 NT_007819.18 11537118
ss39 700054 A/G 2 rs40 0 7 11548657 NT_007819.18 11538657
ss38 700053 C/T 2 rs39 0 7 11548775 NT_007819.18 11538775
ss37 700051 C/G 2 rs38 0 7 11550525 NT_007819.18 11540525
8 of 8 subsnp's starting at ss44.This is the last page.