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
98351 BAA10g05920 A10 3036641 G A upstream_gene_variant MODIFIER c.-3369C>T| S76
98352 BAA10g05920 A10 3036827 G A upstream_gene_variant MODIFIER c.-3555C>T| S153
S213
98353 BAA10g05920 A10 3036953 G A upstream_gene_variant MODIFIER c.-3681C>T| S308
98354 BAA10g05920 A10 3037077 G A upstream_gene_variant MODIFIER c.-3805C>T| S255
98355 BAA10g05920 A10 3038198 C T upstream_gene_variant MODIFIER c.-4926G>A| S121
98356 BAA10g05930 A10 3038876 G A upstream_gene_variant MODIFIER c.-1744G>A| S83
S88
98357 BAA10g05930 A10 3038940 C T upstream_gene_variant MODIFIER c.-1680C>T| S291
S42
98358 BAA10g05930 A10 3039716 G A upstream_gene_variant MODIFIER c.-904G>A| S184
98359 BAA10g05930 A10 3040337 G A upstream_gene_variant MODIFIER c.-283G>A| S92
98360 BAA10g05930 A10 3040925 A T synonymous_variant LOW c.306A>T|p.Ile102Ile S279
98361 BAA10g05930 A10 3041695 C T synonymous_variant LOW c.612C>T|p.Ile204Ile S73
S91
98362 BAA10g05930 A10 3041907 G A missense_variant MODERATE c.824G>A|p.Ser275Asn S261
98363 BAA10g05930 A10 3042006 C T intron_variant MODIFIER c.897+26C>T| S49
98364 BAA10g05930 A10 3042012 C T intron_variant MODIFIER c.897+32C>T| S19
98365 BAA10g05930 A10 3043380 G A downstream_gene_variant MODIFIER c.*656G>A| S207
98366 BAA10g05930 A10 3043529 G A downstream_gene_variant MODIFIER c.*805G>A| S133
98367 BAA10g05930 A10 3044739 C T downstream_gene_variant MODIFIER c.*2015C>T| S189
98368 BAA10g05930 A10 3045638 G A downstream_gene_variant MODIFIER c.*2914G>A| S90
98369 BAA10g05930 A10 3046242 G A downstream_gene_variant MODIFIER c.*3518G>A| S240
98370 BAA10g05930 A10 3046402 C T downstream_gene_variant MODIFIER c.*3678C>T| S233
98371 BAA10g05930 A10 3047502 C T downstream_gene_variant MODIFIER c.*4778C>T| S95
98372 BAA10g05940 A10 3047875 C T downstream_gene_variant MODIFIER c.*4292G>A| S199
S9
98373 BAA10g05940 A10 3048206 G A downstream_gene_variant MODIFIER c.*3961C>T| S95
98374 BAA10g05940 A10 3049372 C T downstream_gene_variant MODIFIER c.*2795G>A| S249
98375 BAA10g05940 A10 3049545 C T downstream_gene_variant MODIFIER c.*2622G>A| S67