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
152201 BAA02g00830 A02 398793 C T missense_variant MODERATE c.191G>A|p.Arg64Lys S228
152202 BAA02g00830 A02 399965 G A upstream_gene_variant MODIFIER c.-607C>T| S199
152203 BAA02g00830 A02 400019 G A upstream_gene_variant MODIFIER c.-661C>T| S223
152204 BAA02g00830 A02 400483 C T upstream_gene_variant MODIFIER c.-1125G>A| S252
152205 BAA02g00830 A02 401518 C T upstream_gene_variant MODIFIER c.-2160G>A| S79
S84
152206 BAA02g00840 A02 403661 C T missense_variant MODERATE c.635G>A|p.Arg212His S262
152207 BAA02g00840 A02 403869 C T missense_variant MODERATE c.427G>A|p.Ala143Thr S177
152208 BAA02g00840 A02 405024 G A upstream_gene_variant MODIFIER c.-633C>T| S11
152209 BAA02g00840 A02 405026 G A upstream_gene_variant MODIFIER c.-635C>T| S122
152210 BAA02g00860 A02 407469 C T splice_acceptor_variant&intron_variant HIGH c.447-1G>A| S172
S217
152211 BAA02g00860 A02 408225 G A missense_variant MODERATE c.59C>T|p.Ser20Phe S64
152212 BAA02g00840 A02 409150 C T upstream_gene_variant MODIFIER c.-4759G>A| S133
152213 BAA02g00870 A02 410166 G A missense_variant MODERATE c.809C>T|p.Thr270Ile S296
152214 BAA02g00870 A02 410617 G A stop_gained HIGH c.538C>T|p.Gln180* S210
S225
152215 BAA02g00870 A02 410920 C T synonymous_variant LOW c.324G>A|p.Gln108Gln S257
152216 BAA02g00870 A02 411385 C T missense_variant MODERATE c.76G>A|p.Ala26Thr S180
152217 BAA02g00860 A02 412086 G A upstream_gene_variant MODIFIER c.-3803C>T| S296
152218 BAA02g00870 A02 414830 C T upstream_gene_variant MODIFIER c.-3370G>A| S277
152219 BAA02g00870 A02 415236 G A upstream_gene_variant MODIFIER c.-3776C>T| S109
152220 BAA02g00870 A02 415655 G A upstream_gene_variant MODIFIER c.-4195C>T| S190
152221 BAA02g00890 A02 417795 G A missense_variant MODERATE c.10G>A|p.Ala4Thr S286
152222 BAA02g00890 A02 418151 C T missense_variant MODERATE c.298C>T|p.Pro100Ser S97
152223 BAA02g00890 A02 419052 G A splice_donor_variant&intron_variant HIGH c.830+1G>A| S136
152224 BAA02g00900 A02 419468 G A upstream_gene_variant MODIFIER c.-770G>A| S23
152225 BAA02g00900 A02 419825 C T upstream_gene_variant MODIFIER c.-413C>T| S241