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
152551 BAA02g01120 A02 535358 G A upstream_gene_variant MODIFIER c.-1736C>T| S238
152552 BAA02g01120 A02 535530 G A upstream_gene_variant MODIFIER c.-1908C>T| S292
152553 BAA02g01120 A02 536689 G A upstream_gene_variant MODIFIER c.-3067C>T| S166
152554 BAA02g01120 A02 537769 G A upstream_gene_variant MODIFIER c.-4147C>T| S41
152555 BAA02g01120 A02 538364 C T upstream_gene_variant MODIFIER c.-4742G>A| S135
152556 BAA02g01130 A02 540909 C T upstream_gene_variant MODIFIER c.-1117G>A| S181
152557 BAA02g01130 A02 541037 G A upstream_gene_variant MODIFIER c.-1245C>T| S297
152558 BAA02g01130 A02 541331 G A upstream_gene_variant MODIFIER c.-1539C>T| S260
152559 BAA02g01140 A02 542822 G A synonymous_variant LOW c.96C>T|p.Asp32Asp S11
152560 BAA02g01130 A02 543367 C T upstream_gene_variant MODIFIER c.-3575G>A| S292
152561 BAA02g01130 A02 543886 G A upstream_gene_variant MODIFIER c.-4094C>T| S249
152562 BAA02g01140 A02 545741 C T upstream_gene_variant MODIFIER c.-2824G>A| S40
S49
152563 BAA02g01140 A02 545881 G A upstream_gene_variant MODIFIER c.-2964C>T| S10
S153
152564 BAA02g01150 A02 545964 G A synonymous_variant LOW c.681C>T|p.Leu227Leu S273
152565 BAA02g01150 A02 546401 C T synonymous_variant LOW c.327G>A|p.Glu109Glu S278
152566 BAA02g01150 A02 546471 C T missense_variant MODERATE c.257G>A|p.Gly86Asp S245
152567 BAA02g01150 A02 546492 G A missense_variant MODERATE c.236C>T|p.Ser79Phe S84
S93
152568 BAA02g01140 A02 547538 C T upstream_gene_variant MODIFIER c.-4621G>A| S47
152569 BAA02g01160 A02 548315 C T missense_variant MODERATE c.367G>A|p.Glu123Lys S186
152570 BAA02g01160 A02 548343 C T synonymous_variant LOW c.339G>A|p.Lys113Lys S13
152571 BAA02g01150 A02 549717 C T upstream_gene_variant MODIFIER c.-2990G>A| S94
152572 BAA02g01150 A02 550412 C T upstream_gene_variant MODIFIER c.-3685G>A| S85
152573 BAA02g01170 A02 550895 C T synonymous_variant LOW c.12C>T|p.Val4Val S207
152574 BAA02g01170 A02 550942 C T missense_variant MODERATE c.59C>T|p.Ser20Leu S262
152575 BAA02g01170 A02 551019 G A missense_variant MODERATE c.136G>A|p.Gly46Arg S265