Data item | Description |
snp_id |
ID of JSNP |
snp_type |
snp type: SNP or IND (insertion/deletion) |
5_flank_seq |
5'-flanking sequence of the snp |
na_var |
nucleic acids variation |
3_flank_seq |
3'-flanking sequence of the snp |
for_primer |
forward primer sequence for e-PCR |
back_primer |
backward primer sequence |
product_size |
PCR product size |
freq_minor |
minor allele frequency of the snp (-1: no frequency information) from JSNP |
freq_major |
major allele frequency of the snp from JSNP |
chr |
chromosome number that the snp is mapped |
chr_start |
start position of the snp in the chromosome |
chr_end |
end position of the snp in the chromosome |
chr_direct |
direction of the flanking sequences against the chromosome |
contig_acc |
ACC of genomic contig (RefSeq NT) that the snp is mapped |
contig_start |
start position of the snp in the genomic contig |
contig_end |
end position of the snp in the genomic contig |
contig_direct |
direction of the flanking sequences against the genomic contig |
hit_count |
number of hit (mapped positions of the snp against genome) |
gene_na_acc |
ACC of a gene (RefSeq NM/XM) that the snp is mapped |
gene_aa_acc |
ACC of the gene (RefSeq NP/XP) that the snp is mapped |
symbol |
symbol of gene that the snp is mapped |
locus_id |
ID of gene (LocusLink) that the snp is mapped |
gene_direct |
direction of the flanking sequences against the direction of the gene:
if the directions of the flanking sequences and of the gene are the same, this is "+"; otherwise "-".
|
str_type |
gene structure that the snp is mapped: CDS, exon, intron, 5'-UTR, 3'-UTR |
aa_var |
amino acids variation |
codon_var |
codon variation |
codon_posi |
snp postion in the codon |
dbsnp_rs_id |
dbSNP rs (reference SNP) number assigned |
dbsnp_ss_id |
dbSNP ss (submitted SNP) number assigned |