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
184451 BAA02g22600 A02 12240502 C T missense_variant MODERATE c.82G>A|p.Glu28Lys S167
184452 BAA02g22600 A02 12241920 G A upstream_gene_variant MODIFIER c.-919C>T| S226
184453 BAA02g22600 A02 12242297 G A upstream_gene_variant MODIFIER c.-1296C>T| S136
184454 BAA02g22600 A02 12243106 C T upstream_gene_variant MODIFIER c.-2105G>A| S203
184455 BAA02g22600 A02 12244070 G A upstream_gene_variant MODIFIER c.-3069C>T| S64
184456 BAA02g22610 A02 12246089 G A upstream_gene_variant MODIFIER c.-863G>A| S35
184457 BAA02g22610 A02 12246180 G A upstream_gene_variant MODIFIER c.-772G>A| S61
184458 BAA02g22610 A02 12247048 G A missense_variant MODERATE c.97G>A|p.Asp33Asn S264
184459 BAA02g22610 A02 12247101 C T synonymous_variant LOW c.150C>T|p.Ile50Ile S205
184460 BAA02g22610 A02 12247562 C T downstream_gene_variant MODIFIER c.*206C>T| S135
184461 BAA02g22610 A02 12247676 C T downstream_gene_variant MODIFIER c.*320C>T| S115
184462 BAA02g22610 A02 12248787 C T downstream_gene_variant MODIFIER c.*1431C>T| S139
184463 BAA02g22610 A02 12249252 C T downstream_gene_variant MODIFIER c.*1896C>T| S221
184464 BAA02g22620 A02 12250281 G A upstream_gene_variant MODIFIER c.-4461G>A| S48
184465 BAA02g22620 A02 12250826 C T upstream_gene_variant MODIFIER c.-3916C>T| S171
184466 BAA02g22620 A02 12251663 G A upstream_gene_variant MODIFIER c.-3079G>A| S176
184467 BAA02g22620 A02 12252412 G A upstream_gene_variant MODIFIER c.-2330G>A| S230
184468 BAA02g22620 A02 12253128 G A upstream_gene_variant MODIFIER c.-1614G>A| S17
184469 BAA02g22620 A02 12253606 C T upstream_gene_variant MODIFIER c.-1136C>T| S13
S168
S239
S279
184470 BAA02g22620 A02 12253740 G A upstream_gene_variant MODIFIER c.-1002G>A| S47
184471 BAA02g22620 A02 12254421 G A upstream_gene_variant MODIFIER c.-321G>A| S172
184472 BAA02g22620 A02 12254992 C T intron_variant MODIFIER c.139+18C>T| S8
184473 BAA02g22620 A02 12255007 G A intron_variant MODIFIER c.139+33G>A| S251
184474 BAA02g22620 A02 12255478 G A missense_variant MODERATE c.491G>A|p.Gly164Glu S247
184475 BAA02g22620 A02 12256527 G A missense_variant MODERATE c.1192G>A|p.Glu398Lys S70