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
154151 BAA02g02480 A02 1119551 C T downstream_gene_variant MODIFIER c.*525C>T| S71
154152 BAA02g02480 A02 1119743 C T downstream_gene_variant MODIFIER c.*717C>T| S124
154153 BAA02g02480 A02 1120348 G A downstream_gene_variant MODIFIER c.*1322G>A| S176
154154 BAA02g02480 A02 1122058 C T downstream_gene_variant MODIFIER c.*3032C>T| S118
154155 BAA02g02490 A02 1123783 C T synonymous_variant LOW c.1986G>A|p.Glu662Glu S46
154156 BAA02g02500 A02 1124880 C T upstream_gene_variant MODIFIER c.-4925C>T| S241
154157 BAA02g02490 A02 1125469 G A synonymous_variant LOW c.1095C>T|p.Ser365Ser S164
154158 BAA02g02490 A02 1125989 G A missense_variant MODERATE c.722C>T|p.Ser241Phe S303
154159 BAA02g02490 A02 1126338 G A missense_variant MODERATE c.457C>T|p.Pro153Ser S264
154160 BAA02g02490 A02 1128792 C T upstream_gene_variant MODIFIER c.-1429G>A| S178
154161 BAA02g02490 A02 1129107 G A upstream_gene_variant MODIFIER c.-1744C>T| S295
154162 BAA02g02490 A02 1129124 G A upstream_gene_variant MODIFIER c.-1761C>T| S84
S93
154163 BAA02g02490 A02 1129389 T C upstream_gene_variant MODIFIER c.-2026A>G| S120
S121
S23
S266
S297
S9
154164 BAA02g02500 A02 1130018 C T stop_gained HIGH c.214C>T|p.Arg72* S204
154165 BAA02g02500 A02 1130093 G A missense_variant MODERATE c.289G>A|p.Glu97Lys S5
154166 BAA02g02510 A02 1133514 C T upstream_gene_variant MODIFIER c.-1141C>T| S302
154167 BAA02g02500 A02 1133768 G A synonymous_variant LOW c.2772G>A|p.Gln924Gln S12
154168 BAA02g02510 A02 1135556 G A synonymous_variant LOW c.555G>A|p.Ala185Ala S269
154169 BAA02g02520 A02 1135778 C T upstream_gene_variant MODIFIER c.-2073C>T| S212
154170 BAA02g02510 A02 1136131 G A stop_gained HIGH c.897G>A|p.Trp299* S273
154171 BAA02g02520 A02 1136475 G A upstream_gene_variant MODIFIER c.-1376G>A| S155
154172 BAA02g02530 A02 1138482 T C upstream_gene_variant MODIFIER c.-2857T>C| S132
S137
S215
154173 BAA02g02530 A02 1140460 G T upstream_gene_variant MODIFIER c.-879G>T| S4
154174 BAA02g02530 A02 1140725 G A upstream_gene_variant MODIFIER c.-614G>A| S13
S140
S168
S219
S279
S64
154175 BAA02g02540 A02 1145187 G A upstream_gene_variant MODIFIER c.-1038G>A| S105
S106