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
157101 BAA02g04900 A02 2138709 C T synonymous_variant LOW c.747C>T|p.Tyr249Tyr S108
157102 BAA02g04900 A02 2138796 G A missense_variant MODERATE c.834G>A|p.Met278Ile S168
157103 BAA02g04900 A02 2139592 G A synonymous_variant LOW c.1212G>A|p.Glu404Glu S89
157104 BAA02g04910 A02 2139673 C T downstream_gene_variant MODIFIER c.*2506G>A| S79
S84
157105 BAA02g04910 A02 2140267 G A downstream_gene_variant MODIFIER c.*1912C>T| S139
157106 BAA02g04900 A02 2141939 G A downstream_gene_variant MODIFIER c.*282G>A| S127
157107 BAA02g04900 A02 2142345 C T downstream_gene_variant MODIFIER c.*688C>T| S277
157108 BAA02g04900 A02 2142514 G A downstream_gene_variant MODIFIER c.*857G>A| S287
157109 BAA02g04920 A02 2143551 C T missense_variant MODERATE c.5722G>A|p.Val1908Met S108
157110 BAA02g04910 A02 2143982 G A upstream_gene_variant MODIFIER c.-1324C>T| S235
157111 BAA02g04910 A02 2144153 C T upstream_gene_variant MODIFIER c.-1495G>A| S234
157112 BAA02g04920 A02 2145181 C T missense_variant MODERATE c.4637G>A|p.Gly1546Glu S249
157113 BAA02g04920 A02 2145186 C T synonymous_variant LOW c.4632G>A|p.Leu1544Leu S112
157114 BAA02g04910 A02 2145978 G A upstream_gene_variant MODIFIER c.-3320C>T| S202
157115 BAA02g04910 A02 2146131 G A upstream_gene_variant MODIFIER c.-3473C>T| S260
157116 BAA02g04920 A02 2146414 C T splice_donor_variant&intron_variant HIGH c.3912+1G>A| S250
157117 BAA02g04920 A02 2146690 C T missense_variant MODERATE c.3721G>A|p.Gly1241Ser S207
157118 BAA02g04920 A02 2147534 G A missense_variant MODERATE c.3200C>T|p.Ser1067Phe S268
157119 BAA02g04920 A02 2148155 C T missense_variant MODERATE c.2821G>A|p.Val941Met S202
157120 BAA02g04920 A02 2148453 G A synonymous_variant LOW c.2634C>T|p.Asn878Asn S122
157121 BAA02g04920 A02 2149273 G A missense_variant MODERATE c.2177C>T|p.Ala726Val S264
157122 BAA02g04920 A02 2149690 C T splice_donor_variant&intron_variant HIGH c.1997+1G>A| S6
157123 BAA02g04920 A02 2150116 G A synonymous_variant LOW c.1657C>T|p.Leu553Leu S155
S211
157124 BAA02g04920 A02 2150266 C T missense_variant MODERATE c.1585G>A|p.Ala529Thr S112
157125 BAA02g04920 A02 2151140 G A synonymous_variant LOW c.1081C>T|p.Leu361Leu S126