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:8.5.98(1)
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
ss57 700067 A/G 2 rs58 0 7 11544019 NT_007819.18 11534019
ss56 700065 G/T 2 rs57 0 7 11544108 NT_007819.18 11534108
ss55 700064 C/G 2 rs56 0 7 11544171 NT_007819.18 11534171
ss54 700063 G/T 2 rs55 0 7 11546001 NT_007819.18 11536001
ss53 700061 C/T 2 rs54 0 7 11546423 NT_007819.18 11536423
ss60 700070 C/G 2 rs61 0 7 11577602 NT_007819.18 11567602
ss59 700069 C/T 2 rs60 0 7 11580535 NT_007819.18 11570535
ss58 700068 C/T 2 rs59 0 7 11580609 NT_007819.18 11570609
8 of 8 subsnp's starting at ss57.This is the last page.