Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
30201 BAA01g21170 A01 10454143 G A downstream_gene_variant MODIFIER c.*4477C>T| S252
30202 BAA01g21160 A01 10454171 C T splice_region_variant&intron_variant LOW c.1421-7C>T| S184
30203 BAA01g21160 A01 10454706 C T synonymous_variant LOW c.1767C>T|p.Leu589Leu S66
30204 BAA01g21160 A01 10454712 C T synonymous_variant LOW c.1773C>T|p.Ser591Ser S231
30205 BAA01g21160 A01 10454830 G A missense_variant MODERATE c.1801G>A|p.Val601Ile S49
30206 BAA01g21160 A01 10456870 G A downstream_gene_variant MODIFIER c.*1846G>A| S180
30207 BAA01g21160 A01 10457460 G T downstream_gene_variant MODIFIER c.*2436G>T| S181
30208 BAA01g21180 A01 10459799 C T upstream_gene_variant MODIFIER c.-4263C>T| S261
30209 BAA01g21180 A01 10460542 C T upstream_gene_variant MODIFIER c.-3520C>T| S100
30210 BAA01g21170 A01 10461720 G A upstream_gene_variant MODIFIER c.-655C>T| S13
S140
S168
S219
S279
S72
30211 BAA01g21170 A01 10461766 C T upstream_gene_variant MODIFIER c.-701G>A| S114
30212 BAA01g21170 A01 10462214 G A upstream_gene_variant MODIFIER c.-1149C>T| S251
30213 BAA01g21170 A01 10462566 G A upstream_gene_variant MODIFIER c.-1501C>T| S140
30214 BAA01g21180 A01 10464108 C T missense_variant MODERATE c.47C>T|p.Pro16Leu S207
30215 BAA01g21180 A01 10464113 C T missense_variant MODERATE c.52C>T|p.Pro18Ser S36
30216 BAA01g21180 A01 10464157 G A synonymous_variant LOW c.96G>A|p.Lys32Lys S241
30217 BAA01g21180 A01 10464270 C T missense_variant MODERATE c.209C>T|p.Ser70Phe S286
30218 BAA01g21180 A01 10464460 G A synonymous_variant LOW c.399G>A|p.Thr133Thr S142
30219 BAA01g21180 A01 10466250 G A downstream_gene_variant MODIFIER c.*1643G>A| S229
30220 BAA01g21180 A01 10466910 C T downstream_gene_variant MODIFIER c.*2303C>T| S100
30221 BAA01g21180-BAA01g21190 A01 10470650 G A intergenic_region MODIFIER n.10470650G>A| S57
30222 BAA01g21180-BAA01g21190 A01 10470768 G A intergenic_region MODIFIER n.10470768G>A| S292
30223 BAA01g21180-BAA01g21190 A01 10470830 G A intergenic_region MODIFIER n.10470830G>A| S187
30224 BAA01g21180-BAA01g21190 A01 10471283 C T intergenic_region MODIFIER n.10471283C>T| S136
30225 BAA01g21180-BAA01g21190 A01 10471609 G A intergenic_region MODIFIER n.10471609G>A| S38