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
95401 BAA10g04100 A10 1997814 G A upstream_gene_variant MODIFIER c.-586C>T| S302
95402 BAA10g04100 A10 2001050 G A upstream_gene_variant MODIFIER c.-3822C>T| S295
95403 BAA10g04100 A10 2001658 G A upstream_gene_variant MODIFIER c.-4430C>T| S172
95404 BAA10g04110 A10 2002100 G A stop_gained HIGH c.163C>T|p.Gln55* S128
95405 BAA10g04110 A10 2005598 G A upstream_gene_variant MODIFIER c.-3336C>T| S48
95406 BAA10g04120 A10 2008378 A T downstream_gene_variant MODIFIER c.*2586T>A| S1
95407 BAA10g04120 A10 2008997 C T downstream_gene_variant MODIFIER c.*1967G>A| S233
95408 BAA10g04120 A10 2010375 G A downstream_gene_variant MODIFIER c.*589C>T| S241
S242
95409 BAA10g04120 A10 2010599 C T downstream_gene_variant MODIFIER c.*365G>A| S249
95410 BAA10g04120 A10 2011813 C T missense_variant MODERATE c.664G>A|p.Ala222Thr S202
95411 BAA10g04120 A10 2012333 G A missense_variant MODERATE c.461C>T|p.Ser154Phe S138
95412 BAA10g04120 A10 2013132 G A upstream_gene_variant MODIFIER c.-251C>T| S280
95413 BAA10g04120 A10 2013512 G A upstream_gene_variant MODIFIER c.-631C>T| S45
95414 BAA10g04120 A10 2015639 G A upstream_gene_variant MODIFIER c.-2758C>T| S133
95415 BAA10g04120 A10 2015843 G A upstream_gene_variant MODIFIER c.-2962C>T| S133
95416 BAA10g04120 A10 2017105 G T upstream_gene_variant MODIFIER c.-4224C>A| S135
95417 BAA10g04120 A10 2017286 G A upstream_gene_variant MODIFIER c.-4405C>T| S112
95418 BAA10g04120 A10 2017751 C T upstream_gene_variant MODIFIER c.-4870G>A| S203
95419 BAA10g04130 A10 2018021 G A downstream_gene_variant MODIFIER c.*4159C>T| S263
95420 BAA10g04130 A10 2019698 C T downstream_gene_variant MODIFIER c.*2482G>A| S208
S93
95421 BAA10g04130 A10 2021080 G A downstream_gene_variant MODIFIER c.*1100C>T| S157
S163
95422 BAA10g04130 A10 2021539 C T downstream_gene_variant MODIFIER c.*641G>A| S155
95423 BAA10g04130 A10 2022315 C T missense_variant MODERATE c.3070G>A|p.Gly1024Arg S259
95424 BAA10g04130 A10 2022801 G A intron_variant MODIFIER c.2896-93C>T| S286
95425 BAA10g04130 A10 2023141 G A intron_variant MODIFIER c.2896-433C>T| S286