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
164401 BAA02g10910 A02 4886329 C T intron_variant MODIFIER c.202-443C>T| S58
164402 BAA02g10910 A02 4887258 C T missense_variant MODERATE c.688C>T|p.Pro230Ser S99
164403 BAA02g10910 A02 4888288 G A missense_variant MODERATE c.1718G>A|p.Gly573Glu S289
S290
164404 BAA02g10910 A02 4888326 C T missense_variant MODERATE c.1756C>T|p.Pro586Ser S71
164405 BAA02g10920 A02 4890496 G A upstream_gene_variant MODIFIER c.-3661G>A| S4
164406 BAA02g10920 A02 4890839 C T upstream_gene_variant MODIFIER c.-3318C>T| S152
164407 BAA02g10920 A02 4890865 C T upstream_gene_variant MODIFIER c.-3292C>T| S306
164408 BAA02g10920 A02 4890894 G A upstream_gene_variant MODIFIER c.-3263G>A| S173
164409 BAA02g10920 A02 4890900 G A upstream_gene_variant MODIFIER c.-3257G>A| S110
164410 BAA02g10920 A02 4890929 G A upstream_gene_variant MODIFIER c.-3228G>A| S144
164411 BAA02g10920 A02 4891363 C T upstream_gene_variant MODIFIER c.-2794C>T| S54
164412 BAA02g10920 A02 4892671 G A upstream_gene_variant MODIFIER c.-1486G>A| S35
164413 BAA02g10920 A02 4892707 C T upstream_gene_variant MODIFIER c.-1450C>T| S5
164414 BAA02g10920 A02 4893606 C T upstream_gene_variant MODIFIER c.-551C>T| S183
S198
164415 BAA02g10920 A02 4893972 C T upstream_gene_variant MODIFIER c.-185C>T| S64
164416 BAA02g10920 A02 4894594 C T synonymous_variant LOW c.438C>T|p.Ser146Ser S185
164417 BAA02g10920 A02 4894606 C T synonymous_variant LOW c.450C>T|p.Asp150Asp S175
164418 BAA02g10920 A02 4894626 C T missense_variant MODERATE c.470C>T|p.Ser157Phe S118
164419 BAA02g10920 A02 4894862 G A missense_variant MODERATE c.706G>A|p.Gly236Arg S303
164420 BAA02g10920 A02 4895188 C T synonymous_variant LOW c.1032C>T|p.Phe344Phe S183
S198
164421 BAA02g10930 A02 4897298 G A downstream_gene_variant MODIFIER c.*1251C>T| S235
164422 BAA02g10920 A02 4898034 C T missense_variant MODERATE c.2437C>T|p.Leu813Phe S156
S34
164423 BAA02g10930 A02 4898709 C T missense_variant&splice_region_variant MODERATE c.2381G>A|p.Gly794Glu S18
164424 BAA02g10930 A02 4899674 G A missense_variant MODERATE c.1702C>T|p.Pro568Ser S169
164425 BAA02g10930 A02 4899701 C T missense_variant MODERATE c.1675G>A|p.Gly559Arg S130