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
175201 BAA02g17790 A02 8850964 G A intron_variant MODIFIER c.643-13C>T| S259
175202 BAA02g17790 A02 8851260 G A intron_variant MODIFIER c.470-40C>T| S289
S290
175203 BAA02g17790 A02 8852864 C T upstream_gene_variant MODIFIER c.-733G>A| S44
175204 BAA02g17790 A02 8853114 C T upstream_gene_variant MODIFIER c.-983G>A| S218
175205 BAA02g17790 A02 8853223 C T upstream_gene_variant MODIFIER c.-1092G>A| S8
175206 BAA02g17790 A02 8854450 C T upstream_gene_variant MODIFIER c.-2319G>A| S71
175207 BAA02g17790 A02 8854744 C T upstream_gene_variant MODIFIER c.-2613G>A| S138
175208 BAA02g17790 A02 8854847 C T upstream_gene_variant MODIFIER c.-2716G>A| S182
175209 BAA02g17800 A02 8856718 C T missense_variant MODERATE c.4679G>A|p.Ser1560Asn S179
175210 BAA02g17800 A02 8856943 C T missense_variant MODERATE c.4454G>A|p.Gly1485Glu S88
175211 BAA02g17800 A02 8857251 G A missense_variant MODERATE c.4325C>T|p.Ala1442Val S87
175212 BAA02g17800 A02 8857281 G A missense_variant MODERATE c.4295C>T|p.Pro1432Leu S236
175213 BAA02g17800 A02 8858231 C T missense_variant MODERATE c.3542G>A|p.Arg1181Lys S206
S26
175214 BAA02g17800 A02 8858266 G A synonymous_variant LOW c.3507C>T|p.Phe1169Phe S236
175215 BAA02g17800 A02 8858529 G A missense_variant MODERATE c.3244C>T|p.Pro1082Ser S303
175216 BAA02g17800 A02 8858628 G A missense_variant MODERATE c.3145C>T|p.Leu1049Phe S162
175217 BAA02g17800 A02 8859196 G A synonymous_variant LOW c.2577C>T|p.Leu859Leu S53
175218 BAA02g17800 A02 8859444 C T intron_variant MODIFIER c.2398-69G>A| S302
175219 BAA02g17800 A02 8859590 G A intron_variant MODIFIER c.2397+138C>T| S279
175220 BAA02g17800 A02 8859662 C T intron_variant MODIFIER c.2397+66G>A| S84
S93
175221 BAA02g17800 A02 8859954 G A missense_variant MODERATE c.2171C>T|p.Pro724Leu S116
175222 BAA02g17800 A02 8860810 C T synonymous_variant LOW c.1494G>A|p.Leu498Leu S87
175223 BAA02g17800 A02 8860960 G A synonymous_variant LOW c.1344C>T|p.His448His S150
175224 BAA02g17800 A02 8861562 C T missense_variant MODERATE c.916G>A|p.Asp306Asn S185
S203
S273
175225 BAA02g17800 A02 8863063 G A intron_variant MODIFIER c.124+160C>T| S81
S85