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
71151 BAA01g37310 A01 24884290 C T upstream_gene_variant MODIFIER c.-3171C>T| S98
71152 BAA01g37310 A01 24884927 G A upstream_gene_variant MODIFIER c.-2534G>A| S245
71153 BAA01g37310 A01 24886280 G A upstream_gene_variant MODIFIER c.-1181G>A| S108
71154 BAA01g37310 A01 24886525 C T upstream_gene_variant MODIFIER c.-936C>T| S94
71155 BAA01g37310 A01 24886835 G A upstream_gene_variant MODIFIER c.-626G>A| S15
S3
71156 BAA01g37310 A01 24887051 A T upstream_gene_variant MODIFIER c.-410A>T| S259
71157 BAA01g37310 A01 24887079 C T upstream_gene_variant MODIFIER c.-382C>T| S284
71158 BAA01g37310 A01 24887769 C T intron_variant MODIFIER c.294+15C>T| S247
71159 BAA01g37310 A01 24889782 C T missense_variant MODERATE c.655C>T|p.Pro219Ser S200
71160 BAA01g37310 A01 24889923 G A splice_donor_variant&intron_variant HIGH c.795+1G>A| S199
71161 BAA01g37310 A01 24890058 C T synonymous_variant LOW c.861C>T|p.Leu287Leu S67
71162 BAA01g37310 A01 24890288 C T missense_variant MODERATE c.1091C>T|p.Ala364Val S69
71163 BAA01g37310 A01 24890352 C T synonymous_variant LOW c.1155C>T|p.Leu385Leu S166
71164 BAA01g37310 A01 24890812 C T missense_variant MODERATE c.1615C>T|p.Pro539Ser S118
71165 BAA01g37310 A01 24891287 G A downstream_gene_variant MODIFIER c.*335G>A| S224
71166 BAA01g37310 A01 24891408 G A downstream_gene_variant MODIFIER c.*456G>A| S74
71167 BAA01g37310 A01 24892937 C T downstream_gene_variant MODIFIER c.*1985C>T| S232
71168 BAA01g37310 A01 24893897 G A downstream_gene_variant MODIFIER c.*2945G>A| S234
71169 BAA01g37310 A01 24894191 G A downstream_gene_variant MODIFIER c.*3239G>A| S271
71170 BAA01g37310-BAA01g37320 A01 24895974 G A intergenic_region MODIFIER n.24895974G>A| S308
71171 BAA01g37310-BAA01g37320 A01 24896233 C T intergenic_region MODIFIER n.24896233C>T| S216
71172 BAA01g37310-BAA01g37320 A01 24897032 A T intergenic_region MODIFIER n.24897032A>T| S91
71173 BAA01g37320 A01 24897239 A G downstream_gene_variant MODIFIER c.*4841T>C| S273
71174 BAA01g37320 A01 24897574 G A downstream_gene_variant MODIFIER c.*4506C>T| S111
71175 BAA01g37320 A01 24898241 C T downstream_gene_variant MODIFIER c.*3839G>A| S219
S72