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
99501 BAA10g06560-BAA10g06570 A10 3420625 C T intergenic_region MODIFIER n.3420625C>T| S159
S243
S298
S299
99502 BAA10g06560-BAA10g06570 A10 3420628 G A intergenic_region MODIFIER n.3420628G>A| S64
99503 BAA10g06560-BAA10g06570 A10 3420735 G A intergenic_region MODIFIER n.3420735G>A| S98
99504 BAA10g06560-BAA10g06570 A10 3422890 C T intergenic_region MODIFIER n.3422890C>T| S263
99505 BAA10g06560-BAA10g06570 A10 3423315 C T intergenic_region MODIFIER n.3423315C>T| S185
99506 BAA10g06560-BAA10g06570 A10 3423526 C T intergenic_region MODIFIER n.3423526C>T| S67
99507 BAA10g06560-BAA10g06570 A10 3423654 C T intergenic_region MODIFIER n.3423654C>T| S176
99508 BAA10g06560-BAA10g06570 A10 3423797 G A intergenic_region MODIFIER n.3423797G>A| S112
99509 BAA10g06560-BAA10g06570 A10 3423926 G A intergenic_region MODIFIER n.3423926G>A| S57
99510 BAA10g06570 A10 3424253 C T downstream_gene_variant MODIFIER c.*4847G>A| S110
99511 BAA10g06570 A10 3424317 C T downstream_gene_variant MODIFIER c.*4783G>A| S155
S211
99512 BAA10g06570 A10 3424370 G A downstream_gene_variant MODIFIER c.*4730C>T| S289
99513 BAA10g06570 A10 3425543 C T downstream_gene_variant MODIFIER c.*3557G>A| S185
99514 BAA10g06570 A10 3425763 G A downstream_gene_variant MODIFIER c.*3337C>T| S240
99515 BAA10g06570 A10 3426731 C T downstream_gene_variant MODIFIER c.*2369G>A| S165
S211
S227
99516 BAA10g06570 A10 3426870 C T downstream_gene_variant MODIFIER c.*2230G>A|
99517 BAA10g06570 A10 3427448 G A downstream_gene_variant MODIFIER c.*1652C>T| S167
99518 BAA10g06570 A10 3427563 C T downstream_gene_variant MODIFIER c.*1537G>A| S92
99519 BAA10g06570 A10 3427610 C T downstream_gene_variant MODIFIER c.*1490G>A| S70
99520 BAA10g06570 A10 3427849 G A downstream_gene_variant MODIFIER c.*1251C>T| S221
99521 BAA10g06570 A10 3428110 G A downstream_gene_variant MODIFIER c.*990C>T| S219
S72
99522 BAA10g06570 A10 3428114 G A downstream_gene_variant MODIFIER c.*986C>T| S296
99523 BAA10g06590 A10 3428711 C T upstream_gene_variant MODIFIER c.-4735C>T| S247
99524 BAA10g06570 A10 3429392 C T missense_variant MODERATE c.380G>A|p.Ser127Asn S132
S137
S215
S89
99525 BAA10g06570 A10 3429869 G A upstream_gene_variant MODIFIER c.-98C>T| S217
S248