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
163501 BAA02g10180 A02 4525428 C T missense_variant MODERATE c.340G>A|p.Ala114Thr S221
163502 BAA02g10180 A02 4526118 G A upstream_gene_variant MODIFIER c.-55C>T| S43
163503 BAA02g10180 A02 4528311 G A upstream_gene_variant MODIFIER c.-2248C>T| S188
163504 BAA02g10190 A02 4528618 C T synonymous_variant LOW c.813G>A|p.Lys271Lys S202
163505 BAA02g10180 A02 4529291 C T upstream_gene_variant MODIFIER c.-3228G>A| S278
163506 BAA02g10190 A02 4529370 G A missense_variant MODERATE c.293C>T|p.Ser98Phe S291
163507 BAA02g10180 A02 4530664 C T upstream_gene_variant MODIFIER c.-4601G>A| S120
163508 BAA02g10190 A02 4531485 C T upstream_gene_variant MODIFIER c.-1635G>A| S18
163509 BAA02g10190 A02 4532061 G A upstream_gene_variant MODIFIER c.-2211C>T| S163
163510 BAA02g10190 A02 4533354 C T upstream_gene_variant MODIFIER c.-3504G>A| S218
163511 BAA02g10210 A02 4534820 A G missense_variant MODERATE c.1249T>C|p.Trp417Arg S53
163512 BAA02g10210 A02 4535180 C T missense_variant MODERATE c.889G>A|p.Glu297Lys S90
163513 BAA02g10210 A02 4535610 C T synonymous_variant LOW c.459G>A|p.Thr153Thr S128
163514 BAA02g10210 A02 4535621 C T missense_variant MODERATE c.448G>A|p.Gly150Arg S230
163515 BAA02g10200 A02 4536092 C T upstream_gene_variant MODIFIER c.-2459G>A| S116
163516 BAA02g10200 A02 4537220 C T upstream_gene_variant MODIFIER c.-3587G>A| S171
163517 BAA02g10200 A02 4538602 G A upstream_gene_variant MODIFIER c.-4969C>T| S206
S26
163518 BAA02g10210 A02 4539449 G A upstream_gene_variant MODIFIER c.-3381C>T| S122
163519 BAA02g10210 A02 4539707 G A upstream_gene_variant MODIFIER c.-3639C>T| S62
163520 BAA02g10210-BAA02g10220 A02 4541304 G A intergenic_region MODIFIER n.4541304G>A| S165
163521 BAA02g10210-BAA02g10220 A02 4543812 G A intergenic_region MODIFIER n.4543812G>A| S295
163522 BAA02g10220 A02 4547209 C T downstream_gene_variant MODIFIER c.*2257G>A| S224
163523 BAA02g10220 A02 4548325 G A downstream_gene_variant MODIFIER c.*1141C>T| S111
163524 BAA02g10220 A02 4549106 G A downstream_gene_variant MODIFIER c.*360C>T| S105
S106
163525 BAA02g10220 A02 4549648 G A missense_variant MODERATE c.130C>T|p.His44Tyr S286