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
116251 BAA10g10160-BAA10g10170 A10 11949056 C T intergenic_region MODIFIER n.11949056C>T| S70
116252 BAA10g10170 A10 11949420 G A downstream_gene_variant MODIFIER c.*4779C>T| S112
116253 BAA10g10170 A10 11949604 C T downstream_gene_variant MODIFIER c.*4595G>A| S155
S211
116254 BAA10g10170 A10 11951011 C T downstream_gene_variant MODIFIER c.*3188G>A| S281
116255 BAA10g10170 A10 11951748 C T downstream_gene_variant MODIFIER c.*2451G>A| S169
116256 BAA10g10170 A10 11952437 C T downstream_gene_variant MODIFIER c.*1762G>A| S84
S93
116257 BAA10g10170 A10 11952585 G A downstream_gene_variant MODIFIER c.*1614C>T| S202
116258 BAA10g10170 A10 11955639 C T splice_acceptor_variant&intron_variant HIGH c.1174-1G>A| S164
116259 BAA10g10170 A10 11955796 G A missense_variant MODERATE c.1102C>T|p.Pro368Ser S179
116260 BAA10g10170 A10 11956996 C T missense_variant MODERATE c.568G>A|p.Gly190Ser S8
116261 BAA10g10170 A10 11957335 G A intron_variant MODIFIER c.424-12C>T| S95
116262 BAA10g10170 A10 11957984 C T intron_variant MODIFIER c.285+50G>A| S56
116263 BAA10g10170 A10 11958025 G A intron_variant MODIFIER c.285+9C>T| S140
116264 BAA10g10170 A10 11958327 G A synonymous_variant LOW c.54C>T|p.Ala18Ala S95
116265 BAA10g10170 A10 11958840 G A upstream_gene_variant MODIFIER c.-460C>T| S13
116266 BAA10g10170 A10 11959894 G A upstream_gene_variant MODIFIER c.-1514C>T| S171
116267 BAA10g10170 A10 11961860 G A upstream_gene_variant MODIFIER c.-3480C>T| S278
116268 BAA10g10170 A10 11962029 G A upstream_gene_variant MODIFIER c.-3649C>T| S286
116269 BAA10g10170 A10 11962284 C T upstream_gene_variant MODIFIER c.-3904G>A| S133
116270 BAA10g10170 A10 11962340 C T upstream_gene_variant MODIFIER c.-3960G>A| S25
116271 BAA10g10170 A10 11962839 G A upstream_gene_variant MODIFIER c.-4459C>T| S136
116272 BAA10g10170 A10 11963180 C T upstream_gene_variant MODIFIER c.-4800G>A| S40
S49
116273 BAA10g10180 A10 11964362 C T upstream_gene_variant MODIFIER c.-1692C>T| S38
116274 BAA10g10180 A10 11965656 C T upstream_gene_variant MODIFIER c.-398C>T| S146
116275 BAA10g10180 A10 11966997 C T missense_variant MODERATE c.554C>T|p.Pro185Leu S63