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
185551 BAA02g23110 A02 12593729 C T downstream_gene_variant MODIFIER c.*1699C>T| S186
185552 BAA02g23110 A02 12594089 G A downstream_gene_variant MODIFIER c.*2059G>A| S148
S30
S31
185553 BAA02g23110 A02 12594903 C T downstream_gene_variant MODIFIER c.*2873C>T| S241
185554 BAA02g23110 A02 12595546 G A downstream_gene_variant MODIFIER c.*3516G>A| S157
185555 BAA02g23110 A02 12596360 G A downstream_gene_variant MODIFIER c.*4330G>A| S295
185556 BAA02g23110 A02 12596745 G A downstream_gene_variant MODIFIER c.*4715G>A| S126
185557 BAA02g23120 A02 12597314 C T missense_variant MODERATE c.916G>A|p.Glu306Lys S289
S290
185558 BAA02g23120 A02 12597408 C T intron_variant MODIFIER c.873+31G>A| S152
185559 BAA02g23120 A02 12597620 C T intron_variant MODIFIER c.721-29G>A| S283
185560 BAA02g23120 A02 12599799 G A upstream_gene_variant MODIFIER c.-889C>T| S37
185561 BAA02g23120 A02 12600350 G A upstream_gene_variant MODIFIER c.-1440C>T| S13
S261
185562 BAA02g23120 A02 12601038 C T upstream_gene_variant MODIFIER c.-2128G>A| S123
185563 BAA02g23120 A02 12601591 G A upstream_gene_variant MODIFIER c.-2681C>T| S111
185564 BAA02g23120 A02 12602298 G A upstream_gene_variant MODIFIER c.-3388C>T| S5
185565 BAA02g23130 A02 12606858 C A upstream_gene_variant MODIFIER c.-1127C>A| S47
185566 BAA02g23130 A02 12607679 C T upstream_gene_variant MODIFIER c.-306C>T| S175
185567 BAA02g23140 A02 12608567 G A upstream_gene_variant MODIFIER c.-3643G>A| S256
185568 BAA02g23130 A02 12609593 G A missense_variant MODERATE c.1258G>A|p.Asp420Asn S246
185569 BAA02g23140 A02 12610139 G A upstream_gene_variant MODIFIER c.-2071G>A| S79
S91
185570 BAA02g23140 A02 12610488 G A upstream_gene_variant MODIFIER c.-1722G>A| S161
185571 BAA02g23140 A02 12612146 G A upstream_gene_variant MODIFIER c.-64G>A| S293
185572 BAA02g23130 A02 12612560 C T downstream_gene_variant MODIFIER c.*2860C>T| S99
185573 BAA02g23140 A02 12612843 G A missense_variant MODERATE c.332G>A|p.Gly111Glu S173
185574 BAA02g23130 A02 12613215 G A downstream_gene_variant MODIFIER c.*3515G>A| S223
185575 BAA02g23140 A02 12617774 C T missense_variant MODERATE c.682C>T|p.His228Tyr S212