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
78201 BAA01g41100 A01 27352574 C T downstream_gene_variant MODIFIER c.*4271C>T| S206
S26
78202 BAA01g41100 A01 27353033 G A downstream_gene_variant MODIFIER c.*4730G>A| S123
78203 BAA01g41100-BAA01g41110 A01 27353685 C T intergenic_region MODIFIER n.27353685C>T| S94
78204 BAA01g41100-BAA01g41110 A01 27353762 C T intergenic_region MODIFIER n.27353762C>T| S133
78205 BAA01g41100-BAA01g41110 A01 27355583 G A intergenic_region MODIFIER n.27355583G>A| S189
78206 BAA01g41100-BAA01g41110 A01 27355821 C T intergenic_region MODIFIER n.27355821C>T| S186
78207 BAA01g41110 A01 27356374 C T upstream_gene_variant MODIFIER c.-4770C>T| S279
78208 BAA01g41110 A01 27357625 C T upstream_gene_variant MODIFIER c.-3519C>T| S54
78209 BAA01g41110 A01 27359471 C T upstream_gene_variant MODIFIER c.-1673C>T| S256
78210 BAA01g41110 A01 27359592 C T upstream_gene_variant MODIFIER c.-1552C>T| S120
78211 BAA01g41110 A01 27360074 C T upstream_gene_variant MODIFIER c.-1070C>T| S53
78212 BAA01g41110 A01 27361304 C T missense_variant MODERATE c.161C>T|p.Pro54Leu S161
78213 BAA01g41130 A01 27361912 C T upstream_gene_variant MODIFIER c.-2116C>T| S16
78214 BAA01g41130 A01 27362256 C T upstream_gene_variant MODIFIER c.-1772C>T| S159
S243
78215 BAA01g41120 A01 27362631 G A missense_variant MODERATE c.434C>T|p.Ser145Leu S287
78216 BAA01g41130 A01 27363276 C T upstream_gene_variant MODIFIER c.-752C>T| S180
78217 BAA01g41130 A01 27363436 G A upstream_gene_variant MODIFIER c.-592G>A| S189
78218 BAA01g41120 A01 27363503 C T missense_variant MODERATE c.19G>A|p.Glu7Lys S275
78219 BAA01g41120 A01 27364674 C T upstream_gene_variant MODIFIER c.-1153G>A| S264
78220 BAA01g41120 A01 27365414 C T upstream_gene_variant MODIFIER c.-1893G>A| S67
78221 BAA01g41140 A01 27366885 C T missense_variant MODERATE c.724G>A|p.Gly242Arg S251
78222 BAA01g41140 A01 27367392 C T missense_variant MODERATE c.283G>A|p.Asp95Asn S92
78223 BAA01g41140 A01 27367650 C T splice_acceptor_variant&intron_variant HIGH c.26-1G>A| S233
78224 BAA01g41120 A01 27367937 C T upstream_gene_variant MODIFIER c.-4416G>A| S167
78225 BAA01g41140 A01 27371233 G A upstream_gene_variant MODIFIER c.-3179C>T| S245