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
184501 BAA02g22620 A02 12256592 G A synonymous_variant LOW c.1257G>A|p.Glu419Glu S189
184502 BAA02g22620 A02 12256915 C T missense_variant MODERATE c.1421C>T|p.Ser474Phe S240
184503 BAA02g22620 A02 12257372 C T synonymous_variant LOW c.1683C>T|p.Val561Val S209
184504 BAA02g22620 A02 12258338 G A missense_variant MODERATE c.2297G>A|p.Arg766Gln S156
184505 BAA02g22620 A02 12258718 G A missense_variant&splice_region_variant MODERATE c.2459G>A|p.Gly820Glu S256
184506 BAA02g22620 A02 12259800 G A missense_variant MODERATE c.3376G>A|p.Glu1126Lys S17
184507 BAA02g22630 A02 12260569 G A upstream_gene_variant MODIFIER c.-3274G>A| S47
184508 BAA02g22630 A02 12260616 G A upstream_gene_variant MODIFIER c.-3227G>A| S173
184509 BAA02g22630 A02 12261216 T C upstream_gene_variant MODIFIER c.-2627T>C| S47
184510 BAA02g22630 A02 12261560 G A upstream_gene_variant MODIFIER c.-2283G>A| S143
184511 BAA02g22630 A02 12261862 C T upstream_gene_variant MODIFIER c.-1981C>T| S182
184512 BAA02g22630 A02 12263978 C T missense_variant MODERATE c.136C>T|p.Pro46Ser S299
184513 BAA02g22630 A02 12264375 C T missense_variant MODERATE c.533C>T|p.Pro178Leu S183
S198
184514 BAA02g22640 A02 12265557 C T upstream_gene_variant MODIFIER c.-3297C>T| S124
184515 BAA02g22640 A02 12267803 G A upstream_gene_variant MODIFIER c.-1051G>A| S30
S31
184516 BAA02g22640 A02 12268979 C T synonymous_variant LOW c.126C>T|p.Tyr42Tyr S167
184517 BAA02g22640 A02 12269359 C T missense_variant MODERATE c.506C>T|p.Thr169Ile S71
184518 BAA02g22640 A02 12270376 C T downstream_gene_variant MODIFIER c.*842C>T| S270
184519 BAA02g22640 A02 12270921 C T downstream_gene_variant MODIFIER c.*1387C>T| S209
184520 BAA02g22650 A02 12272991 G A upstream_gene_variant MODIFIER c.-3480G>A| S19
184521 BAA02g22650 A02 12274329 G A upstream_gene_variant MODIFIER c.-2142G>A| S139
184522 BAA02g22650 A02 12277567 G A intron_variant MODIFIER c.631+466G>A| S92
184523 BAA02g22660 A02 12278963 G A downstream_gene_variant MODIFIER c.*4237C>T| S148
S210
184524 BAA02g22650 A02 12279682 C T missense_variant MODERATE c.878C>T|p.Ser293Phe S242
184525 BAA02g22650 A02 12280003 C T missense_variant MODERATE c.1199C>T|p.Pro400Leu S264