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
75401 BAA01g39730 A01 26383190 G A upstream_gene_variant MODIFIER c.-475G>A| S262
75402 BAA01g39730 A01 26383858 C T missense_variant MODERATE c.194C>T|p.Ala65Val S165
75403 BAA01g39730 A01 26385437 G A downstream_gene_variant MODIFIER c.*723G>A| S76
75404 BAA01g39730 A01 26387823 C T downstream_gene_variant MODIFIER c.*3109C>T| S50
75405 BAA01g39730 A01 26388114 C T downstream_gene_variant MODIFIER c.*3400C>T| S200
75406 BAA01g39730 A01 26388900 G A downstream_gene_variant MODIFIER c.*4186G>A| S143
75407 BAA01g39730 A01 26389578 A G downstream_gene_variant MODIFIER c.*4864A>G| S216
75408 BAA01g39730-BAA01g39740 A01 26390235 C G intergenic_region MODIFIER n.26390235C>G| S215
75409 BAA01g39740 A01 26395891 C T downstream_gene_variant MODIFIER c.*780G>A| S256
75410 BAA01g39750 A01 26396410 C T upstream_gene_variant MODIFIER c.-4942C>T| S16
75411 BAA01g39750 A01 26396711 G A upstream_gene_variant MODIFIER c.-4641G>A| S217
75412 BAA01g39740 A01 26396857 G A synonymous_variant LOW c.628C>T|p.Leu210Leu S294
75413 BAA01g39740 A01 26396880 C T missense_variant MODERATE c.605G>A|p.Gly202Glu S11
75414 BAA01g39740 A01 26398121 G A upstream_gene_variant MODIFIER c.-564C>T| S299
75415 BAA01g39740 A01 26398843 A G upstream_gene_variant MODIFIER c.-1286T>C| S183
S198
75416 BAA01g39740 A01 26400056 G A upstream_gene_variant MODIFIER c.-2499C>T| S263
75417 BAA01g39740 A01 26400751 C T upstream_gene_variant MODIFIER c.-3194G>A| S62
75418 BAA01g39740 A01 26401088 C T upstream_gene_variant MODIFIER c.-3531G>A| S166
75419 BAA01g39740 A01 26401164 C T upstream_gene_variant MODIFIER c.-3607G>A| S186
75420 BAA01g39740 A01 26401171 C T upstream_gene_variant MODIFIER c.-3614G>A| S242
75421 BAA01g39750 A01 26402361 C T synonymous_variant LOW c.279C>T|p.Tyr93Tyr S264
75422 BAA01g39750 A01 26402531 G A missense_variant MODERATE c.449G>A|p.Gly150Glu S280
75423 BAA01g39750 A01 26403899 C T intron_variant MODIFIER c.541-135C>T| S183
S198
75424 BAA01g39750 A01 26405029 C T downstream_gene_variant MODIFIER c.*870C>T| S288
75425 BAA01g39750 A01 26405827 G A downstream_gene_variant MODIFIER c.*1668G>A| S1
S90