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
1601 BAA01g01300 A01 555491 G A downstream_gene_variant MODIFIER c.*1338G>A| S298
1602 BAA01g01300 A01 555776 G A downstream_gene_variant MODIFIER c.*1623G>A| S13
1603 BAA01g01300 A01 555965 C T downstream_gene_variant MODIFIER c.*1812C>T| S203
1604 BAA01g01300 A01 556315 C T downstream_gene_variant MODIFIER c.*2162C>T| S171
1605 BAA01g01310 A01 559632 C T downstream_gene_variant MODIFIER c.*4069C>T| S25
1606 BAA01g01320 A01 560430 C T splice_region_variant&intron_variant LOW c.82+8G>A| S243
1607 BAA01g01320 A01 562654 G A upstream_gene_variant MODIFIER c.-2135C>T| S293
1608 BAA01g01320 A01 563999 G A upstream_gene_variant MODIFIER c.-3480C>T| S195
1609 BAA01g01320 A01 564127 C T upstream_gene_variant MODIFIER c.-3608G>A| S130
1610 BAA01g01320 A01 565195 G A upstream_gene_variant MODIFIER c.-4676C>T| S152
1611 BAA01g01330 A01 565347 C T missense_variant MODERATE c.124C>T|p.Pro42Ser S184
1612 BAA01g01330 A01 565429 G A missense_variant MODERATE c.206G>A|p.Gly69Glu S212
1613 BAA01g01330 A01 565707 A C downstream_gene_variant MODIFIER c.*121A>C| S178
1614 BAA01g01330 A01 566752 C T downstream_gene_variant MODIFIER c.*1166C>T| S81
S85
1615 BAA01g01330 A01 569434 C T downstream_gene_variant MODIFIER c.*3848C>T| S236
1616 BAA01g01330 A01 570181 C T downstream_gene_variant MODIFIER c.*4595C>T| S42
1617 BAA01g01340 A01 571756 C T downstream_gene_variant MODIFIER c.*4391G>A| S244
1618 BAA01g01340 A01 572853 C T downstream_gene_variant MODIFIER c.*3294G>A| S8
1619 BAA01g01340 A01 573715 C T downstream_gene_variant MODIFIER c.*2432G>A| S77
S82
1620 BAA01g01340 A01 573814 G A downstream_gene_variant MODIFIER c.*2333C>T| S63
1621 BAA01g01340 A01 574151 G A downstream_gene_variant MODIFIER c.*1996C>T| S10
1622 BAA01g01340 A01 574323 T A downstream_gene_variant MODIFIER c.*1824A>T| S286
1623 BAA01g01340 A01 576222 C T synonymous_variant LOW c.774G>A|p.Thr258Thr S9
1624 BAA01g01340 A01 579236 G A upstream_gene_variant MODIFIER c.-2056C>T| S23
1625 BAA01g01340 A01 580617 C T upstream_gene_variant MODIFIER c.-3437G>A| S278