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
178401 BAA02g19330 A02 10027204 C T downstream_gene_variant MODIFIER c.*2331C>T| S166
178402 BAA02g19330 A02 10027806 C T downstream_gene_variant MODIFIER c.*2933C>T| S181
178403 BAA02g19330 A02 10027984 G A downstream_gene_variant MODIFIER c.*3111G>A| S173
178404 BAA02g19360 A02 10029304 G A upstream_gene_variant MODIFIER c.-4522G>A| S35
178405 BAA02g19340 A02 10030113 C T missense_variant MODERATE c.100G>A|p.Gly34Ser S15
S3
178406 BAA02g19340 A02 10030994 G A upstream_gene_variant MODIFIER c.-782C>T| S223
178407 BAA02g19350 A02 10032140 C T synonymous_variant LOW c.321G>A|p.Gly107Gly S185
178408 BAA02g19340 A02 10033386 G A upstream_gene_variant MODIFIER c.-3174C>T| S246
178409 BAA02g19340 A02 10033457 G A upstream_gene_variant MODIFIER c.-3245C>T| S251
178410 BAA02g19360 A02 10034074 C T missense_variant MODERATE c.182C>T|p.Ala61Val S179
178411 BAA02g19360 A02 10034201 G A missense_variant MODERATE c.226G>A|p.Ala76Thr S148
S30
S31
178412 BAA02g19360 A02 10034425 G A missense_variant MODERATE c.367G>A|p.Glu123Lys S293
178413 BAA02g19370 A02 10035010 C T missense_variant MODERATE c.769G>A|p.Gly257Arg S130
178414 BAA02g19350 A02 10036614 G A upstream_gene_variant MODIFIER c.-3988C>T| S4
178415 BAA02g19370 A02 10038659 C T upstream_gene_variant MODIFIER c.-2349G>A| S302
178416 BAA02g19370 A02 10040354 G A upstream_gene_variant MODIFIER c.-4044C>T| S146
178417 BAA02g19370 A02 10040599 C T upstream_gene_variant MODIFIER c.-4289G>A| S299
178418 BAA02g19370 A02 10040758 G A upstream_gene_variant MODIFIER c.-4448C>T| S86
178419 BAA02g19380 A02 10041550 G A upstream_gene_variant MODIFIER c.-2897G>A| S173
178420 BAA02g19380 A02 10042381 C T upstream_gene_variant MODIFIER c.-2066C>T| S242
178421 BAA02g19380 A02 10043202 G A upstream_gene_variant MODIFIER c.-1245G>A| S204
178422 BAA02g19380 A02 10043313 A C upstream_gene_variant MODIFIER c.-1134A>C| S41
178423 BAA02g19380 A02 10043530 C T upstream_gene_variant MODIFIER c.-917C>T| S163
178424 BAA02g19380 A02 10043641 G A upstream_gene_variant MODIFIER c.-806G>A| S169
178425 BAA02g19380 A02 10043669 C T upstream_gene_variant MODIFIER c.-778C>T| S185