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
154301 BAA02g02610 A02 1184649 C T splice_region_variant&intron_variant LOW c.1432-6C>T| S66
154302 BAA02g02610 A02 1184810 C T synonymous_variant LOW c.1587C>T|p.Asp529Asp S16
154303 BAA02g02610 A02 1185664 C T synonymous_variant LOW c.2077C>T|p.Leu693Leu S167
154304 BAA02g02620 A02 1185755 G A upstream_gene_variant MODIFIER c.-2423G>A| S217
S248
154305 BAA02g02610 A02 1186094 G A missense_variant MODERATE c.2347G>A|p.Glu783Lys S64
154306 BAA02g02610 A02 1186281 G A splice_region_variant&intron_variant LOW c.2448+8G>A| S265
154307 BAA02g02620 A02 1186888 C T upstream_gene_variant MODIFIER c.-1290C>T| S278
154308 BAA02g02610 A02 1187092 G A synonymous_variant LOW c.2853G>A|p.Lys951Lys S168
154309 BAA02g02620 A02 1188408 G A stop_gained HIGH c.231G>A|p.Trp77* S209
154310 BAA02g02620 A02 1188694 G A missense_variant MODERATE c.517G>A|p.Glu173Lys S162
154311 BAA02g02620 A02 1188739 G A missense_variant MODERATE c.562G>A|p.Glu188Lys S170
154312 BAA02g02620 A02 1188810 G A synonymous_variant LOW c.633G>A|p.Leu211Leu S279
154313 BAA02g02630 A02 1189452 G A upstream_gene_variant MODIFIER c.-3916G>A| S50
154314 BAA02g02630 A02 1191095 C T upstream_gene_variant MODIFIER c.-2273C>T| S198
154315 BAA02g02630 A02 1191507 C T upstream_gene_variant MODIFIER c.-1861C>T| S75
S81
154316 BAA02g02630 A02 1191555 C T upstream_gene_variant MODIFIER c.-1813C>T| S257
154317 BAA02g02630 A02 1191583 G A upstream_gene_variant MODIFIER c.-1785G>A| S289
S290
154318 BAA02g02630 A02 1192968 G A upstream_gene_variant MODIFIER c.-400G>A| S241
154319 BAA02g02620 A02 1193586 C T downstream_gene_variant MODIFIER c.*3711C>T| S171
154320 BAA02g02630 A02 1194492 C T synonymous_variant LOW c.852C>T|p.Thr284Thr S193
154321 BAA02g02630 A02 1196108 C T downstream_gene_variant MODIFIER c.*1523C>T| S288
154322 BAA02g02630 A02 1196377 G A downstream_gene_variant MODIFIER c.*1792G>A| S282
154323 BAA02g02640 A02 1197762 G A missense_variant MODERATE c.4795C>T|p.Pro1599Ser S206
S26
154324 BAA02g02630 A02 1198016 C T downstream_gene_variant MODIFIER c.*3431C>T| S167
154325 BAA02g02640 A02 1199598 G A intron_variant MODIFIER c.3972+68C>T| S163