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
184651 BAA02g22690 A02 12305402 C T stop_gained HIGH c.147G>A|p.Trp49* S33
184652 BAA02g22690 A02 12305808 C T upstream_gene_variant MODIFIER c.-260G>A| S32
184653 BAA02g22690 A02 12306065 C T upstream_gene_variant MODIFIER c.-517G>A| S219
S72
184654 BAA02g22690 A02 12306078 G A upstream_gene_variant MODIFIER c.-530C>T| S155
S211
184655 BAA02g22690 A02 12306153 C T upstream_gene_variant MODIFIER c.-605G>A| S32
184656 BAA02g22690 A02 12307665 C T upstream_gene_variant MODIFIER c.-2117G>A| S118
184657 BAA02g22690 A02 12308041 C T upstream_gene_variant MODIFIER c.-2493G>A| S202
184658 BAA02g22690 A02 12308623 C T upstream_gene_variant MODIFIER c.-3075G>A| S171
184659 BAA02g22690 A02 12308908 C T upstream_gene_variant MODIFIER c.-3360G>A| S186
184660 BAA02g22690 A02 12309401 T G upstream_gene_variant MODIFIER c.-3853A>C| S126
S221
S244
S246
S84
184661 BAA02g22690 A02 12309408 G A upstream_gene_variant MODIFIER c.-3860C>T| S298
184662 BAA02g22690 A02 12310236 C T upstream_gene_variant MODIFIER c.-4688G>A| S277
184663 BAA02g22700 A02 12311395 G A upstream_gene_variant MODIFIER c.-1842G>A| S197
184664 BAA02g22700 A02 12311903 G A upstream_gene_variant MODIFIER c.-1334G>A| S251
184665 BAA02g22700 A02 12312646 C T upstream_gene_variant MODIFIER c.-591C>T| S219
S72
184666 BAA02g22700 A02 12312731 G A upstream_gene_variant MODIFIER c.-506G>A| S23
184667 BAA02g22700 A02 12312737 G A upstream_gene_variant MODIFIER c.-500G>A| S259
184668 BAA02g22700 A02 12313524 C T synonymous_variant LOW c.288C>T|p.His96His S192
184669 BAA02g22720 A02 12315761 G A upstream_gene_variant MODIFIER c.-949G>A| S294
184670 BAA02g22710 A02 12316404 C T missense_variant MODERATE c.115G>A|p.Glu39Lys S289
S290
184671 BAA02g22720 A02 12317037 G A missense_variant MODERATE c.328G>A|p.Glu110Lys S169
184672 BAA02g22720 A02 12317054 C T synonymous_variant LOW c.345C>T|p.Leu115Leu S75
S81
184673 BAA02g22710 A02 12317408 C T upstream_gene_variant MODIFIER c.-890G>A| S265
S39
184674 BAA02g22720 A02 12317963 C T missense_variant MODERATE c.596C>T|p.Ser199Phe S8
184675 BAA02g22720 A02 12318553 C T synonymous_variant LOW c.1047C>T|p.Leu349Leu S56