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
119501 BAA10g11480-BAA10g11490 A10 13078884 C T intergenic_region MODIFIER n.13078884C>T| S169
S38
119502 BAA10g11490 A10 13079754 G A upstream_gene_variant MODIFIER c.-4504G>A| S245
119503 BAA10g11490 A10 13079805 C T upstream_gene_variant MODIFIER c.-4453C>T| S270
119504 BAA10g11490 A10 13079843 C T upstream_gene_variant MODIFIER c.-4415C>T| S47
119505 BAA10g11490 A10 13079855 G A upstream_gene_variant MODIFIER c.-4403G>A| S9
119506 BAA10g11490 A10 13080882 G A upstream_gene_variant MODIFIER c.-3376G>A| S245
119507 BAA10g11490 A10 13081039 C T upstream_gene_variant MODIFIER c.-3219C>T| S79
S91
119508 BAA10g11490 A10 13082105 G A upstream_gene_variant MODIFIER c.-2153G>A| S148
S30
S31
119509 BAA10g11490 A10 13082479 G A upstream_gene_variant MODIFIER c.-1779G>A| S252
119510 BAA10g11490 A10 13082553 C T upstream_gene_variant MODIFIER c.-1705C>T| S200
119511 BAA10g11490 A10 13082565 C T upstream_gene_variant MODIFIER c.-1693C>T| S167
119512 BAA10g11490 A10 13083920 C T upstream_gene_variant MODIFIER c.-338C>T| S73
S91
119513 BAA10g11490 A10 13085537 C T missense_variant MODERATE c.686C>T|p.Pro229Leu S121
119514 BAA10g11490 A10 13085650 C T intron_variant MODIFIER c.718-14C>T| S301
S304
119515 BAA10g11490 A10 13085925 C T downstream_gene_variant MODIFIER c.*35C>T| S162
119516 BAA10g11490 A10 13086123 G A downstream_gene_variant MODIFIER c.*233G>A| S1
S90
119517 BAA10g11490 A10 13086643 C T downstream_gene_variant MODIFIER c.*753C>T| S190
119518 BAA10g11490 A10 13086977 C T downstream_gene_variant MODIFIER c.*1087C>T| S84
S93
119519 BAA10g11490 A10 13087129 C T downstream_gene_variant MODIFIER c.*1239C>T| S2
119520 BAA10g11490 A10 13088103 G A downstream_gene_variant MODIFIER c.*2213G>A| S140
119521 BAA10g11490 A10 13088810 G A downstream_gene_variant MODIFIER c.*2920G>A| S125
119522 BAA10g11490-BAA10g11500 A10 13092743 C T intergenic_region MODIFIER n.13092743C>T| S185
119523 BAA10g11490-BAA10g11500 A10 13094082 G A intergenic_region MODIFIER n.13094082G>A| S45
119524 BAA10g11490-BAA10g11500 A10 13094107 C T intergenic_region MODIFIER n.13094107C>T| S48
119525 BAA10g11490-BAA10g11500 A10 13094523 G A intergenic_region MODIFIER n.13094523G>A| S278