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
36201 BAA01g23860 A01 12475841 C T upstream_gene_variant MODIFIER c.-4768C>T| S295
36202 BAA01g23860 A01 12476511 C T upstream_gene_variant MODIFIER c.-4098C>T| S36
S82
S92
36203 BAA01g23860 A01 12476876 C T upstream_gene_variant MODIFIER c.-3733C>T| S164
S20
36204 BAA01g23860 A01 12476954 G A upstream_gene_variant MODIFIER c.-3655G>A| S240
36205 BAA01g23860 A01 12477279 C T upstream_gene_variant MODIFIER c.-3330C>T| S211
36206 BAA01g23860 A01 12477355 C T upstream_gene_variant MODIFIER c.-3254C>T| S200
36207 BAA01g23860 A01 12477755 G A upstream_gene_variant MODIFIER c.-2854G>A| S32
36208 BAA01g23860 A01 12478320 C T upstream_gene_variant MODIFIER c.-2289C>T| S10
36209 BAA01g23860 A01 12478735 C T upstream_gene_variant MODIFIER c.-1874C>T| S25
36210 BAA01g23860 A01 12480617 G A synonymous_variant LOW c.9G>A|p.Glu3Glu S238
36211 BAA01g23860 A01 12480762 C T intron_variant MODIFIER c.74-50C>T| S125
36212 BAA01g23860 A01 12480884 G A missense_variant MODERATE c.146G>A|p.Gly49Glu S59
36213 BAA01g23860 A01 12481307 G A missense_variant MODERATE c.569G>A|p.Arg190Lys S97
36214 BAA01g23860 A01 12481453 C T intron_variant MODIFIER c.670+45C>T| S39
36215 BAA01g23860 A01 12481898 C T synonymous_variant LOW c.1053C>T|p.Asn351Asn S211
S227
36216 BAA01g23860 A01 12482028 G A missense_variant MODERATE c.1183G>A|p.Glu395Lys S202
36217 BAA01g23860 A01 12482293 G A intron_variant MODIFIER c.1347+101G>A| S58
36218 BAA01g23860 A01 12482618 C T intron_variant MODIFIER c.1348-200C>T| S132
S137
S215
S89
36219 BAA01g23860 A01 12482656 C T intron_variant MODIFIER c.1348-162C>T| S279
36220 BAA01g23860 A01 12482833 C T missense_variant MODERATE c.1363C>T|p.Pro455Ser S61
36221 BAA01g23860 A01 12483057 G A stop_gained HIGH c.1587G>A|p.Trp529* S37
36222 BAA01g23860 A01 12483441 G A missense_variant MODERATE c.1861G>A|p.Asp621Asn S281
36223 BAA01g23860 A01 12484586 G A intron_variant MODIFIER c.2324+682G>A| S131
36224 BAA01g23860 A01 12485912 C T synonymous_variant LOW c.2506C>T|p.Leu836Leu S221
36225 BAA01g23860 A01 12486096 G A downstream_gene_variant MODIFIER c.*23G>A| S268