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
142251 BAA10g27190 A10 21279876 C T upstream_gene_variant MODIFIER c.-1003C>T| S203
142252 BAA10g27190 A10 21280117 C T upstream_gene_variant MODIFIER c.-762C>T| S306
S308
142253 BAA10g27190 A10 21280633 C T upstream_gene_variant MODIFIER c.-246C>T| S247
142254 BAA10g27190 A10 21281508 G A intron_variant MODIFIER c.303+233G>A| S274
142255 BAA10g27190 A10 21281745 C T intron_variant MODIFIER c.303+470C>T| S68
142256 BAA10g27190 A10 21283231 G A missense_variant MODERATE c.520G>A|p.Glu174Lys S131
142257 BAA10g27190 A10 21283307 A G missense_variant MODERATE c.596A>G|p.Gln199Arg S103
142258 BAA10g27190 A10 21283927 G A synonymous_variant LOW c.852G>A|p.Leu284Leu S139
142259 BAA10g27200 A10 21285182 C G upstream_gene_variant MODIFIER c.-2853C>G| S216
142260 BAA10g27200 A10 21285273 G A upstream_gene_variant MODIFIER c.-2762G>A| S146
142261 BAA10g27200 A10 21286695 G A upstream_gene_variant MODIFIER c.-1340G>A| S284
142262 BAA10g27200 A10 21287564 C T upstream_gene_variant MODIFIER c.-471C>T| S246
142263 BAA10g27200 A10 21288483 G A missense_variant MODERATE c.221G>A|p.Gly74Glu S18
142264 BAA10g27200 A10 21289681 G A missense_variant MODERATE c.1072G>A|p.Glu358Lys S71
142265 BAA10g27200 A10 21289809 G A synonymous_variant LOW c.1200G>A|p.Leu400Leu S207
142266 BAA10g27200 A10 21290121 C T intron_variant MODIFIER c.1335+177C>T| S287
142267 BAA10g27200 A10 21290458 C T intron_variant MODIFIER c.1336-64C>T| S23
142268 BAA10g27200 A10 21291988 G A splice_region_variant&intron_variant LOW c.2568+8G>A| S164
142269 BAA10g27200 A10 21292295 C T missense_variant MODERATE c.2737C>T|p.Pro913Ser S225
142270 BAA10g27210 A10 21294038 G A upstream_gene_variant MODIFIER c.-3652G>A| S43
142271 BAA10g27210 A10 21294085 C T upstream_gene_variant MODIFIER c.-3605C>T| S155
S211
142272 BAA10g27210 A10 21294782 G A upstream_gene_variant MODIFIER c.-2908G>A| S59
142273 BAA10g27210 A10 21294852 G A upstream_gene_variant MODIFIER c.-2838G>A| S262
142274 BAA10g27210 A10 21296875 C T upstream_gene_variant MODIFIER c.-815C>T| S195
142275 BAA10g27210 A10 21297798 C T missense_variant MODERATE c.109C>T|p.His37Tyr S221