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
156051 BAA02g04130 A02 1796931 A G upstream_gene_variant MODIFIER c.-2647T>C| S79
S84
156052 BAA02g04150 A02 1799234 G A missense_variant MODERATE c.838G>A|p.Val280Ile S197
156053 BAA02g04150 A02 1800547 C T missense_variant MODERATE c.1637C>T|p.Pro546Leu S234
156054 BAA02g04150 A02 1802057 G A downstream_gene_variant MODIFIER c.*1104G>A| S244
156055 BAA02g04160 A02 1802127 C T missense_variant MODERATE c.85G>A|p.Glu29Lys S242
156056 BAA02g04160 A02 1802534 T A upstream_gene_variant MODIFIER c.-323A>T| S204
156057 BAA02g04160 A02 1802887 C T upstream_gene_variant MODIFIER c.-676G>A| S19
156058 BAA02g04160 A02 1803042 C T upstream_gene_variant MODIFIER c.-831G>A| S94
156059 BAA02g04160 A02 1803151 C T upstream_gene_variant MODIFIER c.-940G>A| S133
156060 BAA02g04160 A02 1804979 C T upstream_gene_variant MODIFIER c.-2768G>A| S87
156061 BAA02g04170 A02 1807711 C T missense_variant MODERATE c.484G>A|p.Val162Ile S202
156062 BAA02g04170 A02 1807964 G A synonymous_variant LOW c.231C>T|p.Phe77Phe S91
156063 BAA02g04170 A02 1808056 C T missense_variant MODERATE c.139G>A|p.Asp47Asn S179
156064 BAA02g04170 A02 1808112 G A missense_variant MODERATE c.83C>T|p.Ser28Phe S149
156065 BAA02g04170 A02 1808165 A G synonymous_variant LOW c.30T>C|p.Ser10Ser S38
156066 BAA02g04170 A02 1810086 G A upstream_gene_variant MODIFIER c.-1892C>T| S110
156067 BAA02g04170 A02 1810253 G A upstream_gene_variant MODIFIER c.-2059C>T| S302
156068 BAA02g04170 A02 1811806 C T upstream_gene_variant MODIFIER c.-3612G>A| S284
156069 BAA02g04170 A02 1811855 G A upstream_gene_variant MODIFIER c.-3661C>T| S157
156070 BAA02g04170 A02 1812784 G A upstream_gene_variant MODIFIER c.-4590C>T| S57
156071 BAA02g04180 A02 1814446 C T missense_variant MODERATE c.136C>T|p.Leu46Phe S200
156072 BAA02g04190 A02 1814601 C T downstream_gene_variant MODIFIER c.*1895G>A| S121
156073 BAA02g04190 A02 1814753 G A downstream_gene_variant MODIFIER c.*1743C>T| S48
156074 BAA02g04180 A02 1814827 C T missense_variant MODERATE c.331C>T|p.Leu111Phe S195
156075 BAA02g04200 A02 1816394 C T upstream_gene_variant MODIFIER c.-4253C>T| S298