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
53551 BAA01g29460 A01 18597855 C T missense_variant MODERATE c.923G>A|p.Gly308Glu S198
53552 BAA01g29450 A01 18598103 G A downstream_gene_variant MODIFIER c.*4352G>A| S32
53553 BAA01g29450 A01 18598204 C T downstream_gene_variant MODIFIER c.*4453C>T| S89
53554 BAA01g29460 A01 18598763 G A intron_variant MODIFIER c.648-204C>T| S244
53555 BAA01g29460 A01 18599851 G A upstream_gene_variant MODIFIER c.-63C>T| S302
53556 BAA01g29470 A01 18605788 G A upstream_gene_variant MODIFIER c.-698C>T| S194
53557 BAA01g29470 A01 18606260 C T upstream_gene_variant MODIFIER c.-1170G>A| S152
53558 BAA01g29470 A01 18606763 C T upstream_gene_variant MODIFIER c.-1673G>A| S117
53559 BAA01g29470 A01 18607002 C T upstream_gene_variant MODIFIER c.-1912G>A| S81
S85
53560 BAA01g29470 A01 18607354 G A upstream_gene_variant MODIFIER c.-2264C>T| S169
S173
53561 BAA01g29470 A01 18607730 G A upstream_gene_variant MODIFIER c.-2640C>T| S86
53562 BAA01g29480 A01 18610500 C T downstream_gene_variant MODIFIER c.*3809C>T| S233
53563 BAA01g29480-BAA01g29490 A01 18611928 C T intergenic_region MODIFIER n.18611928C>T| S35
53564 BAA01g29480-BAA01g29490 A01 18612033 G A intergenic_region MODIFIER n.18612033G>A| S103
53565 BAA01g29480-BAA01g29490 A01 18613317 C T intergenic_region MODIFIER n.18613317C>T| S118
53566 BAA01g29490 A01 18615615 C T upstream_gene_variant MODIFIER c.-3805C>T| S51
53567 BAA01g29490 A01 18618115 G A upstream_gene_variant MODIFIER c.-1305G>A| S116
53568 BAA01g29490 A01 18619379 G A upstream_gene_variant MODIFIER c.-41G>A| S159
S243
53569 BAA01g29490 A01 18619561 G A missense_variant&splice_region_variant MODERATE c.142G>A|p.Val48Met S86
53570 BAA01g29490 A01 18619671 C T intron_variant MODIFIER c.144+108C>T| S279
S51
53571 BAA01g29490 A01 18621159 G A intron_variant MODIFIER c.926+30G>A| S306
S308
53572 BAA01g29490 A01 18621721 C T intron_variant MODIFIER c.1074+39C>T| S35
53573 BAA01g29490 A01 18622042 C T synonymous_variant LOW c.1116C>T|p.Phe372Phe S146
53574 BAA01g29490 A01 18622133 C T intron_variant MODIFIER c.1176+31C>T| S42
53575 BAA01g29490 A01 18622237 C T missense_variant MODERATE c.1219C>T|p.Pro407Ser S142