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
16551 BAA01g12490 A01 5913953 G A upstream_gene_variant MODIFIER c.-975G>A| S116
16552 BAA01g12490 A01 5914532 C T upstream_gene_variant MODIFIER c.-396C>T| S295
16553 BAA01g12490 A01 5914568 C T upstream_gene_variant MODIFIER c.-360C>T| S282
16554 BAA01g12500 A01 5916649 C T upstream_gene_variant MODIFIER c.-863C>T| S260
16555 BAA01g12500 A01 5916972 C T upstream_gene_variant MODIFIER c.-540C>T| S286
16556 BAA01g12500 A01 5918036 C T missense_variant MODERATE c.232C>T|p.His78Tyr S211
S227
16557 BAA01g12500 A01 5918087 G A missense_variant MODERATE c.283G>A|p.Glu95Lys S13
16558 BAA01g12510 A01 5919582 G A synonymous_variant LOW c.453G>A|p.Lys151Lys S235
16559 BAA01g12510 A01 5920008 G A synonymous_variant LOW c.879G>A|p.Thr293Thr S279
16560 BAA01g12510 A01 5920072 G A missense_variant MODERATE c.943G>A|p.Asp315Asn S276
16561 BAA01g12520 A01 5922631 C T upstream_gene_variant MODIFIER c.-542C>T| S136
16562 BAA01g12520 A01 5923106 C T upstream_gene_variant MODIFIER c.-67C>T| S115
S117
S266
S297
S55
S9
16563 BAA01g12520 A01 5923894 G A missense_variant MODERATE c.476G>A|p.Ser159Asn S273
16564 BAA01g12540 A01 5926287 G A upstream_gene_variant MODIFIER c.-2600G>A| S116
16565 BAA01g12530 A01 5928637 C T upstream_gene_variant MODIFIER c.-1754G>A| S158
16566 BAA01g12530 A01 5929426 G A upstream_gene_variant MODIFIER c.-2543C>T| S236
16567 BAA01g12530 A01 5929626 C T upstream_gene_variant MODIFIER c.-2743G>A| S289
S290
16568 BAA01g12550 A01 5932263 C T missense_variant MODERATE c.256C>T|p.Pro86Ser S132
S137
S215
16569 BAA01g12550 A01 5933837 G A missense_variant MODERATE c.1210G>A|p.Glu404Lys S262
16570 BAA01g12550 A01 5934303 G A missense_variant MODERATE c.1565G>A|p.Arg522Lys S245
16571 BAA01g12550 A01 5934681 G A missense_variant MODERATE c.1864G>A|p.Val622Ile S294
16572 BAA01g12550 A01 5935577 C T splice_region_variant&intron_variant LOW c.2592+7C>T| S192
16573 BAA01g12550 A01 5935750 G A synonymous_variant LOW c.2652G>A|p.Ala884Ala S272
16574 BAA01g12570 A01 5936311 C T upstream_gene_variant MODIFIER c.-3120C>T| S35
16575 BAA01g12570 A01 5936369 C T upstream_gene_variant MODIFIER c.-3062C>T| S265