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
44201 BAA01g26890 A01 15165756 C T downstream_gene_variant MODIFIER c.*2221G>A| S38
44202 BAA01g26890 A01 15166684 C T downstream_gene_variant MODIFIER c.*1293G>A| S293
44203 BAA01g26890 A01 15168559 G A intron_variant MODIFIER c.227-188C>T| S144
44204 BAA01g26890 A01 15169176 G A intron_variant MODIFIER c.227-805C>T| S165
44205 BAA01g26890 A01 15169319 C T intron_variant MODIFIER c.227-948G>A| S166
44206 BAA01g26890 A01 15170387 C T intron_variant MODIFIER c.226+1090G>A| S267
44207 BAA01g26890 A01 15170401 C T intron_variant MODIFIER c.226+1076G>A| S177
44208 BAA01g26890 A01 15170629 C T intron_variant MODIFIER c.226+848G>A| S255
44209 BAA01g26890 A01 15170856 G A intron_variant MODIFIER c.226+621C>T| S275
44210 BAA01g26890 A01 15171039 C T intron_variant MODIFIER c.226+438G>A| S176
44211 BAA01g26890 A01 15171379 G A intron_variant MODIFIER c.226+98C>T| S157
44212 BAA01g26890 A01 15171463 G A intron_variant MODIFIER c.226+14C>T| S268
44213 BAA01g26890 A01 15171928 G A upstream_gene_variant MODIFIER c.-226C>T| S149
S62
44214 BAA01g26890 A01 15172093 C T upstream_gene_variant MODIFIER c.-391G>A| S135
44215 BAA01g26890 A01 15173764 G A upstream_gene_variant MODIFIER c.-2062C>T| S37
44216 BAA01g26890 A01 15173842 C T upstream_gene_variant MODIFIER c.-2140G>A| S261
44217 BAA01g26890 A01 15173973 C T upstream_gene_variant MODIFIER c.-2271G>A| S118
44218 BAA01g26890 A01 15174376 G A upstream_gene_variant MODIFIER c.-2674C>T| S142
44219 BAA01g26890 A01 15174387 C T upstream_gene_variant MODIFIER c.-2685G>A| S151
44220 BAA01g26900 A01 15177097 G A downstream_gene_variant MODIFIER c.*769C>T| S45
44221 BAA01g26900 A01 15178092 G A synonymous_variant LOW c.1065C>T|p.Ile355Ile S181
44222 BAA01g26900 A01 15178245 G A intron_variant MODIFIER c.978-66C>T| S86
44223 BAA01g26900 A01 15178413 G A intron_variant MODIFIER c.978-234C>T| S60
44224 BAA01g26900 A01 15178682 G A intron_variant MODIFIER c.977+87C>T| S123
44225 BAA01g26900 A01 15178737 C T intron_variant MODIFIER c.977+32G>A| S208