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
29251 BAA01g20630 A01 10190866 C T upstream_gene_variant MODIFIER c.-1090G>A| S81
29252 BAA01g20630 A01 10191473 C T upstream_gene_variant MODIFIER c.-1697G>A| S51
29253 BAA01g20630 A01 10192146 C T upstream_gene_variant MODIFIER c.-2370G>A| S51
29254 BAA01g20630 A01 10192270 C T upstream_gene_variant MODIFIER c.-2494G>A| S247
29255 BAA01g20630 A01 10192457 C T upstream_gene_variant MODIFIER c.-2681G>A| S108
29256 BAA01g20630 A01 10192868 C T upstream_gene_variant MODIFIER c.-3092G>A| S171
29257 BAA01g20630 A01 10193220 C T upstream_gene_variant MODIFIER c.-3444G>A| S242
29258 BAA01g20630 A01 10193282 G A upstream_gene_variant MODIFIER c.-3506C>T| S87
29259 BAA01g20630 A01 10193524 G A upstream_gene_variant MODIFIER c.-3748C>T| S202
29260 BAA01g20630 A01 10193687 G A upstream_gene_variant MODIFIER c.-3911C>T| S122
29261 BAA01g20630 A01 10194029 C T upstream_gene_variant MODIFIER c.-4253G>A| S179
29262 BAA01g20630 A01 10194168 C T upstream_gene_variant MODIFIER c.-4392G>A| S155
29263 BAA01g20630 A01 10194627 C T upstream_gene_variant MODIFIER c.-4851G>A| S146
29264 BAA01g20630 A01 10194680 G A upstream_gene_variant MODIFIER c.-4904C>T| S235
29265 BAA01g20630 A01 10194717 C T upstream_gene_variant MODIFIER c.-4941G>A| S167
29266 BAA01g20630 A01 10194776 C T upstream_gene_variant MODIFIER c.-5000G>A| S223
29267 BAA01g20640 A01 10195566 G A missense_variant MODERATE c.2243C>T|p.Ser748Leu S296
29268 BAA01g20640 A01 10195668 C T missense_variant MODERATE c.2141G>A|p.Arg714Gln S256
29269 BAA01g20640 A01 10195697 C T synonymous_variant LOW c.2112G>A|p.Arg704Arg S18
29270 BAA01g20640 A01 10195709 G A synonymous_variant LOW c.2100C>T|p.His700His S75
S81
29271 BAA01g20640 A01 10195840 G A missense_variant MODERATE c.1969C>T|p.Pro657Ser S59
29272 BAA01g20640 A01 10195850 C T splice_acceptor_variant&intron_variant HIGH c.1960-1G>A| S85
29273 BAA01g20640 A01 10195897 C T intron_variant MODIFIER c.1960-48G>A| S161
29274 BAA01g20640 A01 10196526 G A intron_variant MODIFIER c.1874+19C>T| S270
29275 BAA01g20640 A01 10196671 C T splice_region_variant&intron_variant LOW c.1752-4G>A| S242