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
185801 BAA02g23380 A02 12737909 G A missense_variant MODERATE c.1145G>A|p.Ser382Asn S37
185802 BAA02g23380 A02 12738550 G A downstream_gene_variant MODIFIER c.*175G>A| S265
185803 BAA02g23380 A02 12739417 C T downstream_gene_variant MODIFIER c.*1042C>T| S296
185804 BAA02g23380 A02 12741870 G A downstream_gene_variant MODIFIER c.*3495G>A| S190
185805 BAA02g23380 A02 12742325 C T downstream_gene_variant MODIFIER c.*3950C>T| S142
185806 BAA02g23380 A02 12743058 G A downstream_gene_variant MODIFIER c.*4683G>A| S177
S51
185807 BAA02g23390 A02 12743617 G A missense_variant MODERATE c.1202C>T|p.Ser401Phe S205
185808 BAA02g23390 A02 12744042 C T synonymous_variant LOW c.777G>A|p.Lys259Lys S206
185809 BAA02g23390 A02 12744217 C T missense_variant MODERATE c.602G>A|p.Gly201Glu S135
185810 BAA02g23390 A02 12744481 G A missense_variant MODERATE c.338C>T|p.Ser113Leu S188
185811 BAA02g23390 A02 12744835 G A upstream_gene_variant MODIFIER c.-17C>T| S136
185812 BAA02g23390 A02 12744898 C T upstream_gene_variant MODIFIER c.-80G>A| S38
185813 BAA02g23390 A02 12745047 C T upstream_gene_variant MODIFIER c.-229G>A| S112
185814 BAA02g23390 A02 12745203 G A upstream_gene_variant MODIFIER c.-385C>T| S50
185815 BAA02g23390 A02 12745438 G A upstream_gene_variant MODIFIER c.-620C>T| S260
185816 BAA02g23390 A02 12745605 C T upstream_gene_variant MODIFIER c.-787G>A| S174
185817 BAA02g23390 A02 12746389 G A upstream_gene_variant MODIFIER c.-1571C>T| S92
185818 BAA02g23400 A02 12746943 G A missense_variant MODERATE c.593C>T|p.Ser198Phe S155
S211
185819 BAA02g23400 A02 12747017 G A synonymous_variant LOW c.519C>T|p.Val173Val S23
185820 BAA02g23400 A02 12748156 G A missense_variant MODERATE c.199C>T|p.Pro67Ser S153
S213
S48
185821 BAA02g23390 A02 12748447 G A upstream_gene_variant MODIFIER c.-3629C>T| S160
185822 BAA02g23410 A02 12749133 C T missense_variant MODERATE c.302C>T|p.Ser101Leu S6
185823 BAA02g23410 A02 12749943 C T missense_variant MODERATE c.773C>T|p.Ser258Leu S115
185824 BAA02g23410 A02 12750208 C T synonymous_variant LOW c.1038C>T|p.Gly346Gly S117
185825 BAA02g23410 A02 12750386 G A missense_variant MODERATE c.1216G>A|p.Ala406Thr S10