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
165701 BAA02g11880 A02 5362695 G A downstream_gene_variant MODIFIER c.*3150C>T| S95
165702 BAA02g11880 A02 5363150 G A downstream_gene_variant MODIFIER c.*2695C>T| S126
165703 BAA02g11880 A02 5363699 C T downstream_gene_variant MODIFIER c.*2146G>A| S207
165704 BAA02g11880 A02 5364180 G A downstream_gene_variant MODIFIER c.*1665C>T| S164
165705 BAA02g11880 A02 5364319 C T downstream_gene_variant MODIFIER c.*1526G>A| S5
165706 BAA02g11880 A02 5365911 C T synonymous_variant LOW c.762G>A|p.Lys254Lys S58
165707 BAA02g11880 A02 5366025 C T synonymous_variant LOW c.648G>A|p.Leu216Leu S240
165708 BAA02g11880 A02 5366352 C T synonymous_variant LOW c.321G>A|p.Gly107Gly S46
165709 BAA02g11880 A02 5367368 G A upstream_gene_variant MODIFIER c.-696C>T| S264
165710 BAA02g11880 A02 5368024 C T upstream_gene_variant MODIFIER c.-1352G>A| S139
165711 BAA02g11890 A02 5368105 C T synonymous_variant LOW c.288G>A|p.Arg96Arg S179
165712 BAA02g11880 A02 5369056 G A upstream_gene_variant MODIFIER c.-2384C>T| S105
S106
165713 BAA02g11880 A02 5371288 A T upstream_gene_variant MODIFIER c.-4616T>A| S271
165714 BAA02g11890 A02 5372405 G A upstream_gene_variant MODIFIER c.-3932C>T| S53
165715 BAA02g11890 A02 5372933 G A upstream_gene_variant MODIFIER c.-4460C>T| S287
165716 BAA02g11890 A02 5373155 C T upstream_gene_variant MODIFIER c.-4682G>A| S200
165717 BAA02g11890 A02 5373237 C T upstream_gene_variant MODIFIER c.-4764G>A| S89
165718 BAA02g11900 A02 5373640 G A upstream_gene_variant MODIFIER c.-2742G>A| S225
165719 BAA02g11900 A02 5373731 C T upstream_gene_variant MODIFIER c.-2651C>T| S6
165720 BAA02g11900 A02 5374252 G A upstream_gene_variant MODIFIER c.-2130G>A| S291
165721 BAA02g11900 A02 5376132 G A upstream_gene_variant MODIFIER c.-250G>A| S41
165722 BAA02g11900 A02 5376968 G A intron_variant MODIFIER c.306-12G>A| S223
165723 BAA02g11900 A02 5377297 G A missense_variant MODERATE c.623G>A|p.Gly208Glu S81
165724 BAA02g11900 A02 5377802 G A downstream_gene_variant MODIFIER c.*372G>A| S197
165725 BAA02g11900 A02 5379109 C T downstream_gene_variant MODIFIER c.*1679C>T| S216
S265
S39